Cancer-Related Fatigue, Version 2.2015

Authors:
Ann M. Berger
Search for other papers by Ann M. Berger in
Current site
Google Scholar
PubMed
Close
 PhD, APRN
,
Kathi Mooney
Search for other papers by Kathi Mooney in
Current site
Google Scholar
PubMed
Close
 RN, PhD
,
Amy Alvarez-Perez
Search for other papers by Amy Alvarez-Perez in
Current site
Google Scholar
PubMed
Close
 MD
,
William S. Breitbart
Search for other papers by William S. Breitbart in
Current site
Google Scholar
PubMed
Close
 MD
,
Kristen M. Carpenter
Search for other papers by Kristen M. Carpenter in
Current site
Google Scholar
PubMed
Close
 PhD
,
David Cella
Search for other papers by David Cella in
Current site
Google Scholar
PubMed
Close
 PhD
,
Charles Cleeland
Search for other papers by Charles Cleeland in
Current site
Google Scholar
PubMed
Close
 PhD
,
Efrat Dotan
Search for other papers by Efrat Dotan in
Current site
Google Scholar
PubMed
Close
 MD
,
Mario A. Eisenberger
Search for other papers by Mario A. Eisenberger in
Current site
Google Scholar
PubMed
Close
 MD
,
Carmen P. Escalante
Search for other papers by Carmen P. Escalante in
Current site
Google Scholar
PubMed
Close
 MD
,
Paul B. Jacobsen
Search for other papers by Paul B. Jacobsen in
Current site
Google Scholar
PubMed
Close
 PhD
,
Catherine Jankowski
Search for other papers by Catherine Jankowski in
Current site
Google Scholar
PubMed
Close
 PhD
,
Thomas LeBlanc
Search for other papers by Thomas LeBlanc in
Current site
Google Scholar
PubMed
Close
 MD, MA
,
Jennifer A. Ligibel
Search for other papers by Jennifer A. Ligibel in
Current site
Google Scholar
PubMed
Close
 MD
,
Elizabeth Trice Loggers
Search for other papers by Elizabeth Trice Loggers in
Current site
Google Scholar
PubMed
Close
 MD, PhD
,
Belinda Mandrell
Search for other papers by Belinda Mandrell in
Current site
Google Scholar
PubMed
Close
 PhD, RN
,
Barbara A. Murphy
Search for other papers by Barbara A. Murphy in
Current site
Google Scholar
PubMed
Close
 MD
,
Oxana Palesh
Search for other papers by Oxana Palesh in
Current site
Google Scholar
PubMed
Close
 PhD, MPH
,
William F. Pirl
Search for other papers by William F. Pirl in
Current site
Google Scholar
PubMed
Close
 MD
,
Steven C. Plaxe
Search for other papers by Steven C. Plaxe in
Current site
Google Scholar
PubMed
Close
 MD
,
Michelle B. Riba
Search for other papers by Michelle B. Riba in
Current site
Google Scholar
PubMed
Close
 MD, MS
,
Hope S. Rugo
Search for other papers by Hope S. Rugo in
Current site
Google Scholar
PubMed
Close
 MD
,
Carolina Salvador
Search for other papers by Carolina Salvador in
Current site
Google Scholar
PubMed
Close
 MD
,
Lynne I. Wagner
Search for other papers by Lynne I. Wagner in
Current site
Google Scholar
PubMed
Close
 PhD
,
Nina D. Wagner-Johnston
Search for other papers by Nina D. Wagner-Johnston in
Current site
Google Scholar
PubMed
Close
 MD
,
Finly J. Zachariah
Search for other papers by Finly J. Zachariah in
Current site
Google Scholar
PubMed
Close
 MD
,
Mary Anne Bergman
Search for other papers by Mary Anne Bergman in
Current site
Google Scholar
PubMed
Close
, and
Courtney Smith
Search for other papers by Courtney Smith in
Current site
Google Scholar
PubMed
Close
 PhD
Full access

Cancer-related fatigue is defined as a distressing, persistent, subjective sense of physical, emotional, and/or cognitive tiredness or exhaustion related to cancer or cancer treatment that is not proportional to recent activity and interferes with usual functioning. It is one of the most common side effects in patients with cancer. Fatigue has been shown to be a consequence of active treatment, but it may also persist into posttreatment periods. Furthermore, difficulties in end-of-life care can be compounded by fatigue. The NCCN Clinical Practice Guidelines in Oncology (NCCN Guidelines) for Cancer-Related Fatigue provide guidance on screening for fatigue and recommendations for interventions based on the stage of treatment. Interventions may include education and counseling, general strategies for the management of fatigue, and specific nonpharmacologic and pharmacologic interventions. Fatigue is a frequently underreported complication in patients with cancer and, when reported, is responsible for reduced quality of life. Therefore, routine screening to identify fatigue is an important component in improving the quality of life for patients living with cancer.

NCCN Categories of Evidence and Consensus

Category 1: Based upon high-level evidence, there is uniform NCCN consensus that the intervention is appropriate.

Category 2A: Based upon lower-level evidence, there is uniform NCCN consensus that the intervention is appropriate.

Category 2B: Based upon lower-level evidence, there is NCCN consensus that the intervention is appropriate.

Category 3: Based upon any level of evidence, there is major NCCN disagreement that the intervention is appropriate.

All recommendations are category 2A unless otherwise noted.

Clinical trials: NCCN believes that the best management for any cancer patient is in a clinical trial. Participation in clinical trials is especially encouraged.

Overview

Fatigue is a common symptom in patients with cancer. It is nearly universal in those receiving cytotoxic chemotherapy, radiation therapy, bone marrow transplantation, or treatment with biologic response modifiers.13 According to a survey of 1569 patients with cancer, fatigue is experienced by 80% of individuals who receive chemotherapy and/or radiotherapy.4,5 In patients with metastatic disease, the prevalence of cancer-related fatigue (CRF) exceeds 75%.69 Using a cutpoint of 4 or higher for moderate fatigue and 7 or higher for severe fatigue on a 0- to 10-point scale, moderate to severe fatigue was reported by 983 of 2177 patients (45%) who were undergoing active outpatient treatment, and 150 of 515 survivors (29%) experiencing complete remission from breast, prostate, colorectal, or lung cancer.10 Cancer survivors report that fatigue is a disruptive symptom experienced months or even years after treatment ends.1118 The distinction between tiredness, fatigue, and exhaustion has not been made in practice, despite conceptual differences.19,20 Patients perceive fatigue to be the most distressing symptom associated with cancer and its treatment, more distressing even than pain or nausea and vomiting, which can generally be managed using medications.21

Fatigue in patients with cancer has been underreported, underdiagnosed, and undertreated. Persistent CRF affects quality of life (QOL), because patients become too tired to fully participate in the roles and activities that make life meaningful.13,22 Health care professionals have been challenged in their efforts to help patients manage this distressful symptom and to remain as fully engaged in life as possible. Because of the successes in cancer treatment, health care professionals are now likely to see patients with prolonged states of fatigue related to the late effects of treatment. Disability-related issues are relevant and often challenging, especially for patients with cancer who are cured of the malignancy but have continued fatigue.23 Despite biomedical literature documenting this entity, it is often difficult

F1

NCCN Clinical Practice Guidelines in Oncology: Cancer-Related Fatigue, Version 2.2015

Version 2.2015, 01-22-15 ©2015 National Comprehensive Cancer Network, Inc. All rights reserved. The NCCN Guidelines® and this illustration may not be reproduced in any form without the express written permission of NCCN®.

Citation: Journal of the National Comprehensive Cancer Network J Natl Compr Canc Netw 13, 8; 10.6004/jnccn.2015.0122

F2

NCCN Clinical Practice Guidelines in Oncology: Cancer-Related Fatigue, Version 2.2015

Version 2.2015, 01-22-15 ©2015 National Comprehensive Cancer Network, Inc. All rights reserved. The NCCN Guidelines® and this illustration may not be reproduced in any form without the express written permission of NCCN®.

Citation: Journal of the National Comprehensive Cancer Network J Natl Compr Canc Netw 13, 8; 10.6004/jnccn.2015.0122

F3

NCCN Clinical Practice Guidelines in Oncology: Cancer-Related Fatigue, Version 2.2015

Version 2.2015, 01-22-15 ©2015 National Comprehensive Cancer Network, Inc. All rights reserved. The NCCN Guidelines® and this illustration may not be reproduced in any form without the express written permission of NCCN®.

Citation: Journal of the National Comprehensive Cancer Network J Natl Compr Canc Netw 13, 8; 10.6004/jnccn.2015.0122

for patients with CRF to obtain or retain disability benefits from insurers. Health care professionals should advocate for patients who require disability benefits, and educate insurers about this issue.

Despite the prevalence of CRF, the specific mechanisms involved in its pathophysiology are unknown. Proposed mechanisms include proinflammatory cytokines,2426 hypothalamic-pituitary-adrenal (HPA) axis dysregulation,24 circadian rhythm desynchronization,27 skeletal muscle wasting,28 and genetic dysregulation29; however, limited evidence supports these proposed mechanisms.

To address the important problem of CRF, NCCN convened a panel of experts. The NCCN Guidelines for Cancer-Related Fatigue, first published in 200030 and updated annually, synthesize the available research and clinical experience in this field and provide recommendations for patient care.

Defining Cancer-Related Fatigue

The panel defines CRF as a distressing, persistent, subjective sense of physical, emotional, and/or cognitive tiredness or exhaustion related to cancer or cancer treatment that is not proportional to recent activity and interferes with usual functioning. Compared with the fatigue experienced by healthy individuals, CRF is more severe, more distressing, and less likely to be relieved by rest. In terms of the defining characteristics, the subjective sense of tiredness reported by the patient is important to note. As with pain, the clinician must rely on the description of fatigue and accompanying distress provided by the patient. Fatigue that interferes with usual functioning is another substantial component of the definition for CRF and the source of much distress for patients.31 Investigations have documented a significant effect of fatigue on physical functioning during cancer treatment, and whether patients regain full functioning when treatment is complete is uncertain.32,33

Standards of Care for Assessment and Management

The panel developed the Standards of Care for CRF Management using the NCCN Clinical Practice Guidelines in Oncology (NCCN Guidelines) for Adult Cancer Pain and for Distress Management as exemplar models (see “Standards of Care for Cancer-Related Fatigue in Children/Adolescents and Adults,” page 1014 [FT-2]; to view the most recent versions of all NCCN Guidelines, visit NCCN.org). These fatigue standards represent the best level of care for the assessment and management of fatigue in patients with cancer, including children, adolescents, and adults, and should provide guidance for health care professionals as they implement these guidelines in their respective institutions and clinical settings. The overall goal of the standards and guidelines is to ensure that all patients with cancer experiencing fatigue are identified and given prompt, effective treatment.

The first standard recognizes fatigue as a subjective experience that should be systematically assessed using patient self-reports and other sources of data. Because it is a symptom that is perceived by the patient, fatigue can be described most accurately through self-report. The history and physical examination, laboratory data, and descriptions of patient behavior provided by family members, especially regarding children, are important sources of additional information.

Fatigue should be screened, assessed, and managed in most patients according to the clinical practice guidelines. The NCCN Guidelines provide “best care” information based on current evidence to support treatment.34 Patients should be screened for the presence and severity of fatigue at their initial clinical visit, at appropriate intervals during and after cancer treatment, and as clinically indicated. Screening should identify fatigue. Patients and families should be informed that managing fatigue is an integral part of total health care. All patients should receive symptom management. Furthermore, if patients cannot tolerate their cancer treatment or if they must choose between treatment and QOL, control of their disease may be diminished.35

Health care professionals experienced in fatigue evaluation and management should be available for consultation in a timely manner. The guidelines for fatigue are best implemented by an interdisciplinary institutional committee, including experts in medicine, nursing, social work, physical therapy, and nutrition.36 The panel recognizes that education and training programs are needed to prepare oncology experts in fatigue management. These are now being offered, but much more attention to these programs within the institutional setting is necessary if professionals are to become skilled in managing fatigue. Variation exists among institutions regarding which professional disciplines and staff can provide appropriate specialized consultation for fatigue. Therefore, in addition to implementation of fatigue treatment guidelines, health care providers should familiarize themselves with the type of supportive care staff available at their institution.

The NCCN Panel recommends that assessment of CRF levels be included in outcomes research. Quality of fatigue management should be included in institutional continuous quality improvement projects. Institutions can make faster progress in implementing these guidelines if they monitor adherence and progress with the recommendations. Medical care contracts should reimburse for managing fatigue, including referrals to a physical therapist, dietitian, or the institution's symptom management service. Disability insurance should include coverage for the continuing effects of fatigue that lead to persistent disability. Rehabilitation should begin with a cancer diagnosis and should continue even after cancer treatment ends.

Guidelines for Evaluation and Treatment

The general schema of the fatigue algorithm defines 4 phases: screening, primary evaluation, intervention, and reevaluation. During the first phase, the health care professional must screen for fatigue and, if present, assess the intensity level. If the intensity level is moderate to severe, the health care professional is directed during the primary evaluation phase of the algorithm to conduct a more focused history and physical examination. This phase also includes an in-depth fatigue assessment and an evaluation of concurrent symptoms and contributing factors frequently associated with fatigue, and can be treated as an initial step in managing fatigue. If, however, a patient either does not have one of these treatable contributing factors or continues to have moderate to severe fatigue after treatment of the factors, the health care professional should recommend additional treatment based on the NCCN Guidelines for CRF.

After the evaluation phase, the guidelines delineate a set of interventions for the amelioration of fatigue based on clinical status (ie, active cancer treatment, posttreatment, end of life). Education and counseling are believed to be central to the effective management of fatigue. Additional interventions that are both nonpharmacologic and pharmacologic may be introduced; in many instances a combination of approaches must be used. The treatment of fatigue is continuous and, as indicated by the reevaluation of patients, leads to an iterative loop of fatigue screening and management. Regardless of whether a patient demonstrates moderate to severe fatigue, health care professionals should continue to monitor for fatigue both throughout and after treatment, because fatigue symptoms have been shown to persist for years. Although no studies have evaluated the long-term treatment of fatigue, it should be assessed and measures should be taken to reduce its impact on QOL.

Screening

The first phase of the algorithm emphasizes the screening of every patient for the presence or absence of fatigue. If fatigue is present, a quantitative or semiquantitative assessment should be performed and documented. For example, on a 0 to 10 numeric rating scale (0 = no fatigue; 10 = worst fatigue imaginable), mild fatigue is indicated as a score of 1 to 3, moderate fatigue as 4 to 6, and severe fatigue as 7 to 10. The evaluation of fatigue in children may be simplified to a scale of 1 to 5 and modified even further in young children (age 5–6 years) who may be asked more simply if they are “tired” or “not tired.”2,3739 If the screening process determines that fatigue is absent or at a mild level, the patient and family should receive education and common management strategies for fatigue. Periodic rescreening and re-evaluation are recommended. Inpatients should be screened daily and outpatients should be screened at subsequent routine and follow-up visits. Survivors and patients who have completed treatment must still be monitored for fatigue, because fatigue may exist beyond the period of active treatment.40

Valid and reliable instruments are available to measure fatigue in children, adolescents, and adults (Table 1, available online, in these guidelines, at NCCN.org [MS-23]); however, the effectiveness of these methods is limited without adequate implementation. Currently, screening is not systematic or effective in many practice settings for various reasons, which often include patient or family barriers and clinician barriers. For example, patients may not want to bother their health care professional in the clinic or office or when they are hospitalized. Patients are also concerned that if they report high levels of fatigue, they might have their treatment altered. Patients do not want to be perceived as complaining, and therefore may not mention fatigue. Or, they may assume that they must live with fatigue, because they believe there is no treatment for it.

Health care professionals may not start a discussion about fatigue for many of the same reasons. First, clinicians may not recognize that fatigue is a problem for the patient. As a symptom, fatigue has been unrecognized and untreated, whereas medical advances have led to better control over the more noticeable or less subtle acute symptoms of nausea, vomiting, and pain. More recently, researchers have begun to document the prevalence and incidence of fatigue, correlating these data with the degree of disruption to QOL.4143 Second, health care professionals may not be aware that effective treatments are available for fatigue despite a lack of knowledge about the underlying pathophysiology and mechanisms.

Given these barriers, screening for CRF must be emphasized. Clinical experience with fatigue assessment has shown that some patients cannot put a numeric value on their fatigue. Consequently, some patients may need to rate fatigue as mild, moderate, or severe. In some circumstances, other sources of data must be used. For example, the patient may not be aware that fatigue has negatively affected his or her life; the spouse, parents, or other family members may be more cognizant of these changes and the effect of fatigue in the patient.

Using the numeric rating scale (ie, 0–10), fatigue studies in patients with cancer have revealed a marked decrease in physical functioning at the level of 7 or higher.44 In another study, ratings of symptom interference guided the selection of numeric rating cutpoints for the levels of mild, moderate, and severe fatigue. Interference levels on the MD Anderson Symptom Inventory (MDASI) scale were found to be well differentiated with the cutpoints for mild, moderate, or severe fatigue.10 Based on these validated levels of fatigue intensity, the panel believes that the numeric rating scale can be used as a guide in practice settings and decision-making.

Primary Evaluation Phase

Focused History and Physical Examination

When fatigue is rated as moderate to severe, with a score of 4 to 10, a more focused history and physical examination should be conducted as part of the primary evaluation phase outlined in the algorithm. One component of this evaluation is an assessment of the patient's current disease status, which encompasses the type and length of treatment, its capacity to induce fatigue, and the patient's response to treatment (see “Primary Evaluation,” page 1016 [FT-4]). If possible, clinicians should determine whether the fatigue is related to a recurrence of the malignancy for those patients assumed to be disease-free or whether it is related to a progression of the malignancy for patients with underlying disease. This is often an important factor causing patients with fatigue to seek further evaluation. If clinicians determine that the fatigue is not related to disease recurrence, informing patients and family members will substantially reduce their anxiety levels. In addition to cancer treatment, clinicians should be aware of any other prescription or over-the-counter medications and supplements the patient is taking.

As part of a focused history, a review of systems should be completed. This review may be helpful in determining the various organ systems affected and in directing the physical evaluation and diagnostic workup. Another component of the focused history is an in-depth fatigue assessment that includes evaluation of several aspects of fatigue: onset, pattern, duration, change over time, associated or alleviating factors, and interference with function. Other physical, emotional, and cognitive symptoms may be associated with fatigue. The health care professional must evaluate the effect of fatigue on normal functioning, including effects on daily living or enjoyable activities. Because fatigue is a subjective condition involving a combination of symptoms and is experienced and reported differently by each person, it is important that the in-depth assessment includes the patient's self-assessment of the causes of fatigue.

The panel also recognized the important role of social support throughout the course of cancer treatment and survivorship (reviewed by Given et al45). Fatigue is a major cause of functional dependence for patients with cancer, especially among the elderly.46 Besides assisting with daily living, caregivers provide cancer-specific support, such as monitoring treatment side effects, aiding in fatigue and pain management, and administering medicine.47 The availability of dependable caregivers can significantly impact the functional, emotional, and financial capacity of a patient coping with cancer and pursuant fatigue. A support network also can be provided when the patient lacks the economic and supportive resources to obtain tangible support.

Assessment of Concurrent Symptoms and Treatable Contributing Factors

As part of this focused evaluation, the NCCN Panel identified factors that are often causative elements in the fatigue experience and, therefore, should be specifically assessed. These factors include pain, emotional distress, sleep disturbance, poor sleep hygiene, anemia, nutrition, activity level, medication side effects profiles, alcohol/substance abuse, and comorbidities.

Descriptive studies have shown that, in adults and children, fatigue seldom occurs alone; it more commonly clusters with sleep disturbance, poor sleep hygiene, emotional distress (eg, depression, anxiety), or pain.4851 Assessment of pain along with emotional distress and institution of effective treatment are essential. In a randomized controlled trial (RCT) of 152 patients with advanced cancer, protocol patient-tailored treatment of the accompanying physical symptoms was coordinated by a nurse and resulted in a higher impact on fatigue than standard oncologic care.52

Fatigue and depression have been documented as concurrent symptoms in patients with cancer. Hopwood and Stephens53 documented depression in 33% of 987 patients with lung cancer and found that fatigue was an independent predictor of depression in this group. In 457 patients with Hodgkin's disease, Loge et al54 found that 26% of patients had fatigue for 6 months or longer (defined as fatigue “cases”) and that fatigue correlated moderately with depression (r=.41).

Sleep disturbances are a neglected problem in oncology55 and may range from hypersomnia to insomnia.56,57 Sleep disturbances are prevalent in 30% to 75% of patients with cancer.58 Several studies have shown that patients with cancer experiencing fatigue during active treatment spend increased time resting and sleeping but that their pattern of sleep is often severely disrupted. When sleep disturbances are present, the patient should be assessed for depression, because this is a common manifestation.59 Patients may benefit from evaluation and education to improve sleep quality. In addition, sleep apnea can develop as a consequence of cancer treatment in the settings of surgery affecting the upper airway, changes in body composition, and alterations in hormone status (eg, thyroid, estrogen, testosterone); therefore, obstructive sleep apnea should also be evaluated.

Poor sleep hygiene behaviors are frequent in patients with cancer. Factors that contribute to poor sleep hygiene include poor individual habits, a poor sleep environment, or an inability to decompress before bedtime. Habits that may be an issue include deviating from a regular sleep schedule, napping during the daytime, and ingesting caffeine, alcohol, or high-sugar foods before bed. An environment conducive to sleep should be dark, quiet, and comfortable to improve sleep quality. Positive sleep hygiene habits include sleeping in a dark room and engaging in activities to reduce stress before bedtime, such as reading, journaling, yoga, meditation, or listening to quiet music. Although all patients should be aware of factors that hinder sleep hygiene, younger patients are especially prone to some of these factors, including late-night gaming, TV watching, computer and cell phone use, and social media use in the hours that interfere with sleep. Both adults and school-aged patients should also be assessed for anxiety that may arise from work or school and the concern of falling behind.

Patients should undergo a nutritional assessment to evaluate weight gain and loss, caloric intake changes, impediments to nutritional intake, anemia, and fluid and electrolyte imbalances. Weight and weight changes should be carefully noted. The health care provider should review and discuss changes in caloric intake with the patient. If there are substantial abnormalities, consultation with a nutrition expert may be appropriate. Often fatigue symptoms can be lessened through improving anemia and modifying dietary intake with appropriate caloric exchanges. Imbalances in sodium, potassium, calcium, iron, and magnesium serum levels are often reversible and, with appropriate supplementation, may reduce fatigue. Nutritional intake may be affected by nausea, vomiting, loss of appetite, food disinterest, mucositis, odynophagia, bowel obstruction, diarrhea, and constipation.

Patients with moderate to severe fatigue should be queried about their functional status, including changes in exercise or activity patterns and the influence of deconditioning. Can patients accomplish normal daily activities? Can they participate in formal or informal exercise programs? What is the amount and frequency of exercise? Has the patient modified exercise or other activity patterns since the development of fatigue? This assessment is important when formulating a treatment plan that may include exercise. Exercise has been beneficial in lowering fatigue levels in certain populations of patients with cancer.60,61 However, before recommending an exercise program, the health care provider or exercise expert (eg, physiatrist, physical therapist) should assess the conditioning level of the patient. It is often difficult to convince fatigued patients that exercise will improve their symptoms. It may be best to begin with discussions and low-level activities, which gradually increase over time. This is especially important if the patient is significantly deconditioned.

Review of current medications (including over-the-counter, herbal, vitamins, and other supplements) is essential. Recent medication changes should also be noted. Medications and medication interactions may contribute to the worsening of fatigue. For example, certain cardiac medications (such as β-blockers) may elicit bradycardia and subsequent fatigue. Combinations of different classes of medications (such as narcotics, antidepressants, antiemetics, and antihistamines) may contribute to excessive drowsiness and increasing fatigue. It may be appropriate to delete or adjust the dose of medications to treat fatigue. In some cases, altering either the dosage or dosing interval of a medication may be sufficient to improve the condition.

During the examination, health care providers should also be alert for signs of alcohol or substance abuse. These detrimental habits can often lead to or aggravate other health problems, such as sleep disturbance, and result in fatigue.

Noncancer comorbidities may contribute substantially to symptoms of fatigue in patients with cancer. Therefore, the status of comorbidities must be reviewed in conjunction with the present treatment management strategies. If the comorbidity is not optimally managed, it may be necessary to further evaluate and improve management. For example, if a patient has underlying congestive heart failure secondary to anthracycline cardiomyopathy and is experiencing symptoms of dyspnea and angina, fatigue may often be improved by stabilizing the condition and decreasing the frequency of episodes of congestive heart failure. This may entail introduction of new medications, titration of current medications, or both. It may also involve an invasive interventional assessment of the patient's cardiac status. Comorbidities that need review and assessment include cardiac, pulmonary, renal, gastrointestinal, hepatic, neurologic, and endocrine dysfunction (including hot flashes, hypothyroidism, hypogonadism, or adrenal insufficiency), and infection. Canaris et al62 noted the high incidence of thyroid dysfunction in “normal” individuals and in patients receiving thyroid medications; they suggested that more attention be given to thyroid problems in both the general population and patients with cancer. Development of hypothyroidism occurs after radiation therapy for Hodgkin disease and other non-Hodgkin's lymphomas, head and neck cancers, and breast cancer, and after total body irradiation in bone marrow transplantation. Hypothyroidism has been noted in patients who have received interferon alfa-2b, aldesleukin (interleukin-2), l-asparaginase, and a multitude of combination chemotherapies. Hypogonadism is commonly seen in patients with advanced cancer. A recent cross-sectional pilot study by Strasser et al63 explored whether hypogonadism contributes to fatigue in men with advanced cancer. Data indicate that abnormally low levels of testosterone are associated with fatigue. However, additional research in a larger patient population is needed to clarify the incidence of hypogonadism and its association with specific malignancies and neurotoxic chemotherapy.

Patient Clinical Status

After the primary fatigue evaluation is completed, the patient's clinical status (active cancer treatment, posttreatment with no active treatment except hormonal therapy, or end of life) should be determined because of its influence on CRF management and treatment strategies. However, some general treatment guidelines apply across all clinical categories.64

If any of the treatable contributing factors discussed earlier is identified during the primary evaluation phase, it should be treated as an initial approach to fatigue management. Other NCCN Guidelines are also available to guide supportive care, including those for Adult Cancer Pain, Distress Management, Cancer- and Chemotherapy-Induced Anemia, Antiemesis, and the Prevention and Treatment of Cancer-Related Infections (to view the most recent version of these guidelines, visit NCCN.org). Treatment of sleep disturbances, poor sleep hygiene, nutritional alterations, and physical deconditioning are discussed under “Nonpharmacologic Interventions” for patients on active treatment, posttreatment, or at end of life in the NCCN Guidelines for Survivorship and for Palliative Care (to view the most recent versions of these guidelines, visit NCCN.org).

Interventions for Patients on Active Treatment

Education and Counseling of Patient and Family

Education about fatigue and its natural history should be offered to all patients with cancer, but it is particularly essential for patients beginning potential fatigue-inducing treatments (such as radiation, chemotherapy, or biotherapy), before onset. Patients should be informed that if fatigue does occur, it may be a consequence of the treatment and is not necessarily an indication that the treatment is not working or that the disease is progressing. This reassurance is important, because fear of progression is a main reason for the underreporting of fatigue. Daily self-monitoring of fatigue levels in a treatment log or diary can be helpful.

General Strategies for Management of Fatigue

In addition to education, the panel recommends counseling for patients about general strategies (energy conservation and distraction) that can be useful in coping with fatigue. Energy conservation is defined as the deliberately planned management of one's personal energy resources to prevent their depletion. It encompasses a common sense approach that helps patients set realistic expectations, prioritize and pace activities, and delegate less-essential activities.65 Patients should be counseled that it is permissible to postpone all nonessential activities if they are experiencing moderate to severe fatigue. One useful plan is to maintain a daily and weekly diary that allows patients to ascertain peak energy periods and then plan activities accordingly within a structured routine. A multisite clinical trial of energy conservation in 296 patients receiving cancer treatment reported significantly lower fatigue in patients receiving the experimental intervention.66 Some participants in the descriptive studies suggested that activities designed to distract (eg, games, music, reading, socializing) are helpful in decreasing fatigue, although the mechanism is unknown. Daytime naps can replenish energy, but it is advisable to limit these to less than an hour to avoid disturbing nighttime sleep. Patients may also use labor-saving techniques, such as wearing a bath robe instead of drying off with a towel, or using devices, including a walker, grabbing tools, and a bedside commode.

Emphasis should be given to finding meaning in the current situation, focusing on meaningful interactions, and promoting the dignity of the patient.

Nonpharmacologic Interventions

Of the specific nonpharmacologic interventions during active cancer treatment, physical activity (category 1), physically based therapies (category 1), and psychosocial interventions (category 1) have the strongest evidence base for treating fatigue; however, nutritional consultation and cognitive behavioral therapy (CBT) for sleep have some supporting evidence.67 These interventions align with recommendations from the Oncology Nursing Society (ONS).6870 Both ASCO71 and the pan-Canadian practice guidelines72 used the ADAPTE method to take advantage of these existing guidelines (ie, NCCN, ONS) to enhance efficient production, reduce duplication, and promote the local update of quality guideline recommendations by their organizations.

Physical Activity: In patients with cancer, the adverse effects of therapy result in decreased activity and physical performance. Although several factors contribute to the decline in functionality, fatigue is one of the major contributors. Mustian et al73 conducted a study in patients receiving systemic chemotherapy to determine the impact of fatigue on physical function as measured by the Activities of Daily Living (ADLs) Index. Of the 753 patients enrolled, 64% were female. In the first and second cycles of chemotherapy, 85.4% and 79.3% of patients reported fatigue, respectively. The mean severity of fatigue was 5.0 for the first cycle and 4.7 for the second cycle (scale of 0–10, with 10 = severe fatigue). CRF interfered with all ADLs in most patients. Interference was moderate, and was noted to be higher in women, non-whites, and patients with metastatic disease.

A large number of small- to moderate-sized studies have been performed to evaluate the feasibility of interventions designed to increase physical activity during therapy, and to explore the impact of increased activity on CRF, QOL, treatment-related side effects, and other end points. A thorough review of the impact of physical activity on these varied outcomes is beyond the scope of this discussion. However, many of these studies have specifically evaluated the effect of increased activity on CRF, and several meta-analyses have been conducted in recent years to provide a comprehensive evaluation of the impact of increased activity on CRF.

The largest meta-analysis to date included 70 studies and 4881 patients with cancer during or after treatment.74 Exercise reduced CRF by a mean effect of 0.32 (95% CI, 0.21–0.43) and 0.38 (95% CI, 0.21–0.54) during and after cancer therapy, respectively.74 A 2012 Cochrane analysis included 56 randomized trials (n=4826), 36 of which were conducted among participants undergoing active cancer treatment.75 Exercise resulted in a decrease in fatigue from baseline to 12 weeks' follow-up (standardized mean difference [SMD], −0.38; 95% CI, −0.57 to −0.18) or when comparing differences in follow-up scores at 12 weeks (SMD,−0.73; 95% CI, −1.14 to −0.31). Systematic reviews have correlated exercise with improvement in fatigue for patients with prostate cancer76 and lymphoma,77 and in those who have undergone hematopoietic cell transplant.78 Other smaller analyses confirmed a significant effect of exercise intervention on fatigue.7983

It is reasonable to encourage all patients to engage in a moderate level of physical activity during and after cancer treatment. Currently evidence is insufficient to recommend a specific amount of physical activity. The US Surgeon General recommends 30 minutes of moderate activity most days of the week for all populations.84 Some observational and interventional studies have suggested that patients with cancer who engage in at least 3 to 5 hours of moderate activity per week may experience better outcomes and have fewer side effects of therapy, including fatigue.60,8589

Patients may require referrals to exercise specialists (eg, physical therapist, physical medicine or rehabilitation specialist) for assessment and an exercise prescription. The American College of Sports Medicine recently developed a certification program for cancer rehabilitation that is available for exercise professionals who specialize in the care of patients with cancer. They also convened a roundtable discussion and published specific guidelines for physical activity testing and exercise programs for patients with cancer.90

Specific issues that should trigger a referral for physical therapy include:

  • Patients with comorbidities (eg, cardiovascular disease or chronic obstructive pulmonary disease)

  • Recent major surgery

  • Specific functional or anatomic deficits (eg, decreased range of motion due to neck dissection in patients with head and neck cancer)

  • Substantial deconditioning

Exercise interventions must be used with caution in patients with any of the following:

  • Bone metastases

  • Thrombocytopenia (low platelets)

  • Anemia (low red blood cells)

  • Fever or active infection

  • Limitations secondary to metastasis or other comorbid illnesses

The exercise program itself should be individualized based on the patient's age, gender, type of cancer, and physical fitness level. Consider cancer-specific exercise programs if available. The program should begin at a low level of intensity and duration, progress slowly, and be modified as the patient's condition changes.

Physically Based Therapies: Therapies performed on the patient by a therapist or layperson include acupuncture and massage therapy. Positive effects of acupuncture on fatigue have been reported in small samples and need to be confirmed with RCTs.91 These small trials were conducted during active non-palliative radiation therapy92,93 and postchemotherapy treatment.94,95 One RCT (n=230)96 and one retrospective review (n=1290)97 reported positive effects of massage therapy on fatigue during active therapy. A decade after these publications, the data remain limited; 2 systemic reviews suggest that acupuncture may have beneficial properties, although the studies acknowledge that a paucity of data makes it difficult to definitively evaluate the benefits.98,99 For further guidance on physical activity, see the NCCN Guidelines for Survivorship (to view the most recent version of these guidelines, visit NCCN.org).

Complementary Therapies: Complementary therapies, such as massage therapy,96,97,100 yoga,101105 muscle relaxation, and stress reduction based on mindfulness,106108 have been evaluated alone or in combination with CBT approaches. The data suggest that these therapies may be effective in reducing fatigue in patients with cancer. Several recent RCTs have demonstrated that yoga intervention, compared with standard care, was effective in lowering CRF during radiotherapy103 and in survivors.101,104,105 However, most of the trials have been conducted in women with breast cancer, and more data are needed to establish the effectiveness of yoga in reducing fatigue in men and in individuals with other cancers.102

Psychosocial Interventions: Patients should be counseled about coping with fatigue and educated about anxiety and depression, which are commonly associated with fatigue during cancer treatment.109 Although a strong correlation exists between emotional distress and fatigue, the precise relationship is not clearly understood.

Studies testing interventions to decrease fatigue can be grouped as CBTs/behavioral therapy (BT), psychoeducational therapies/educational therapies, and supportive expressive therapies, based on review of 3 meta-analyses.81,110,111 Of note, the categories in which interventions have been grouped are different in each of the meta-analyses and have been compared with the work reported by the ONS's Putting Evidence into Practice (PEP) initiative.69,70,112 These studies can be categorized based on their primary outcome parameter: fatigue or other. In many studies, fatigue was a secondary end point measured by a single item or a subscale of an instrument designed to measure emotional distress, QOL, or general symptom burden. Furthermore, fatigue was not an eligibility requirement. In studies specifically designed to measure fatigue, no severity cutoff score was used. Thus, patients enrolled in these studies may or may not have had significant levels of fatigue, thereby limiting the potential impact of the intervention.

Current knowledge regarding CRF includes the following proposed mechanisms: 5-HT3 neurotransmitter deregulation, vagal afferent activation, alteration in muscle and adenosine triphosphate metabolism, HPA axis dysfunction, circadian rhythm dysfunction, and cytokine deregulation. Current psychosocial interventional studies may target one or more of these biologic mechanisms; however, most studies to date fail to identify the underlying targeted mechanism. The exception includes interventions aimed at increasing relaxation, thereby diminishing stress and activation of the HPA axis. Because of the inherent difficulty of conducting mechanistically based interventions, most studies to date have been designed to address educational and coping deficits in order to optimize the patient's ability to deal with this often debilitating symptom.

In addition to the issues noted earlier, outcome parameters used by investigators are highly variable. Currently published studies generally use patient's self-reporting exclusively as the outcome measure. Most studies do not reflect the impact of fatigue on function, report on fatigue-related behaviors, or use objective measures of functionality (eg, the 6-minute walk).

Several meta-analyses evaluated the impact of psychosocial interventions on CRF. Analyzing 41 studies on 3620 patients with cancer, Kangas et al81 reported a weighted pooled mean effect of −0.31 for psychosocial interventions on fatigue. Goedendorp et al110 reported that of 27 RCTs included in their analysis, 7 showed significantly reduced fatigue. Of interest, 80% of fatigue-specific interventions were effective, compared with 14% of nonspecific strategies. Jacobsen et al111 analyzed 30 RCTs and found a significant effect for psychological interventions but not for activity-based programs. A meta-analysis by Duijts et al80 reported that, like exercise programs, behavioral techniques, including cognitive therapy, relaxation techniques, counseling, social support, hypnosis, and biofeedback, are beneficial in improving fatigue among patients with breast cancer during and after treatment. Substantial data in the literature provide high-level evidence during active treatment for CBT/BT106,113116 and psychoeducational therapies/educational therapies.32,67,117124 Supportive expressive therapies (eg, in-person or online support groups, counseling, journal writing) may serve as an emotional outlet and as a support network. There is less-robust evidence for supportive expressive therapies during active treatment; therefore, their use is a category 2A recommendation.

Nutrition Consultation: Many patients with cancer have changes in nutritional status. Because cancer and treatment can interfere with dietary intake, nutrition consultation may be helpful in managing the nutritional deficiencies that result from anorexia, diarrhea, nausea, and vomiting.125 Adequate hydration and electrolyte balance are also essential in preventing and treating fatigue.

Sleep Therapy: Patients with cancer report significant disturbances in sleep patterns that could cause or exacerbate fatigue. Both insomnia and hypersomnia are common, with disrupted sleep as a common denominator. Nonpharmacologic interventions designed to improve sleep quality have been organized into 4 general types of therapies that include cognitive-behavioral, complementary, psychoeducation/information, and exercise therapies.126 Some have also been shown to decrease fatigue.112

There are numerous types of CBT; the most frequently used include stimulus control, sleep restriction, and sleep hygiene. Stimulus control includes going to bed when sleepy, going to bed at approximately the same time each night, and maintaining a regular rising time each day. Getting out of bed after 20 minutes if unable to fall asleep, both when first going to bed and when awakening during the night, is a key aspect of stimulus control. Sleep restriction requires avoiding long or late afternoon naps and limiting total time in bed.127 Techniques to promote a good night's sleep and optimal functioning the next day, such as avoiding caffeine after noon and establishing an environment that is conducive to sleep (eg, dark, quiet, comfortable) are components of sleep hygiene. These strategies were used in a pilot study with women during adjuvant breast cancer chemotherapy. Sleep/wake patterns remained consistent with normal values except for increased number and length of nighttime awakenings.128 For children with cancer, a consistent bedtime and routine, an environment conducive for sleeping, and the presence of security objects (such as blankets and toys) are effective measures (see “Assessment of Concurrent Symptoms and Treatable Contributing Factors,” page 1023).

Pharmacologic Interventions

Although a wide variety of prescription pharmacologic options are available to improve sleep quality, little empirical evidence exists for the use of these agents in patients with cancer, and their use may be associated with adverse side effect profiles. Clinicians need to be aware of the FDA warning regarding the potential risks associated with sedative-hypnotic drugs, including severe allergic reactions and complex sleep-related behaviors, including sleep-driving.129 A table summarizing the medications commonly used to promote sleep is provided on the NCI Physician Data Query Web site.130 Prescribing considerations for these classes of agents include increased likelihood of problems with daytime sleepiness, fatigue, withdrawal symptoms, dependency, rebound insomnia, problems with sleep maintenance, memory problems, anticholinergic symptoms, orthostasis, and the potential for drug-drug interactions involving the cytochrome p450 isoenzyme system. Increased public and professional education regarding sleep, sleep hygiene, sleep disturbances, and daytime consequences of sleep loss are recommended.

Some evidence supports pharmacologic therapy as a fatigue treatment, although a significant placebo response has been observed in a randomized trial.131 Studies on the selective serotonin reuptake inhibitor paroxetine showed no influence by this antidepressant on fatigue in patients receiving chemotherapy.132,133 Antidepressants are not recommended to reduce fatigue. See the relevant NCCN Guidelines for Supportive Care for details on the management of pain, emotional distress, emesis, and anemia (available at NCCN.org). Treatment for nutritional deficit or imbalance and comorbidities may be optimized as indicated.

The psychostimulant methylphenidate has been evaluated for its effect on CRF, with mixed results in patients undergoing cancer therapy. A pilot study found a benefit in fatigue scores in 12 patients with melanoma undergoing interferon-based treatment compared with historical controls.134 However, a randomized, placebo-controlled trial of d-threomethylphenidate to prevent fatigue during radiotherapy for brain tumors did not demonstrate efficacy for the drug in preventing fatigue.135 Similarly, an RCT of 57 women receiving adjuvant chemotherapy for breast cancer failed to show a difference between the active arm and placebo.136 Most recently, Moraska et al137 reported results of a double-blinded phase III trial, in which 148 patients, most of whom were receiving chemotherapy, were randomized to methylphenidate (54 mg/d) or placebo for 4 weeks. No difference in fatigue score was observed between the groups; however, a subset analysis found a benefit with the psychostimulant in patients with severe fatigue and/or advanced disease (P=.02). Analyzing 5 RCTs, Minton et al138 attributed a significant benefit to psychostimulants in alleviating fatigue compared with placebo (z score=2.83; P=.005). Patients have reported minor side effects with methylphenidate, including headache and nausea.

The wakefulness-promoting nonamphetamine psychostimulant modafinil has been approved for use in narcolepsy. In a large RCT, Jean-Pierre et al139 randomized 867 patients undergoing chemotherapy to 200 mg/d of modafinil or placebo. Of the 631 evaluable patients, 315 received modafinil and 316 received placebo. Improvement in fatigue was observed in patients with severe fatigue (P=.017), but not in those with mild or moderate fatigue. Toxicity was similar between the 2 arms. More recently, a phase III randomized, placebo-controlled trial measured the improvement in fatigue in patients with metastatic prostate or breast cancer undergoing docetaxel chemotherapy.140 Fatigue was measured using the MDASI scale, and no statistically significant difference was seen between treatment arms (35.9 vs 39.6; 95% CI, −8.9 to 1.4; P=.15). An increase in toxicity was seen, with patients experiencing grade 2 or higher nausea and vomiting in the modafinil arm (45.4% vs 25%). Because of the limited number of studies and the marginal improvement in CRF in response to modafinil, it is not a recommended treatment.

The use of dietary supplements to alleviate the symptoms of fatigue has yielded mixed results. Although coenzyme Q10 and l-carnitine were evaluated and showed no benefit,141,142 limited data may support the use of ginseng. In a phase III RCT of 364 patients experiencing cancer-related fatigue, improvement of symptoms was observed, as measured by the Multidimensional Fatigue Symptom Inventory-Short Form (MFSI-SF), following treatment with 2000 mg of Wisconsin ginseng.143 In the overall population, improvement at 4 weeks was not statistically significant (ginseng, 14.4 points; SD, 27.1, vs placebo, 8.2 points; SD, 24.8; P=.07). However, at 8 weeks a statistically significant improvement (P=.003) was observed in patients receiving ginseng (20 points; SD, 27) versus patients given the placebo (10.3 points; SD, 26.1). Furthermore, improvement was greatest in patients undergoing active cancer treatment compared with those who had completed treatment. Statistical significance was observed at 4 weeks in the patients undergoing active treatment (P=.02) compared with the after-treatment group (P=.86), with an even greater improvement over placebo at 8 weeks (active treatment, P=.01 vs posttreatment, P=.07). These values were based on the percent change from baseline measured by the MFSI-SF.

After a review of the current literature, the NCCN Panel included consideration of the psychostimulant methylphenidate as a recommendation for treating fatigue in patients undergoing active cancer treatment when other causes of fatigue have been excluded. The data were not sufficient to support the recommendation for modafinil.

Interventions for Patients Posttreatment

More than 11 million US residents now living have a history of cancer. Of the approximately 1,658,370 persons in the United States who will be diagnosed with cancer in 2015, 68% are expected to survive at least 5 years.144 These improvements in survival have led to efforts to enhance symptom management, QOL, and overall functioning of individuals posttreatment. As previously mentioned, fatigue can be an acute effect of cancer or treatment, but it can also be a long-term or late effect.145 Patients may continue to report unusual fatigue for months or years after treatment cessation.11,12,1418 Researchers have suggested that such fatigue may be due to persistent activation of the immune system11,146 or to other factors, including the late effects of treatment on major organ systems.146 However, there are few longitudinal studies examining fatigue in long-term disease-free survivors.

Incidence and prevalence rates for fatigue in this population range from 17% to 21% when strict ICD-10 diagnostic criteria are applied,147 and range from 33% to 53% when other criteria (such as a score of 4 or more on the 0–10 fatigue scale) are used.148 In contrast to these findings, Canadian and US ovarian cancer survivors (n=100), who were diagnosed a mean of 7.2 years before the survey, reported equivalent energy levels when compared with the general population.149 As a consequence, what constitutes valid incidence and prevalence rates in disease-free patients requires more study. Variation of prevalence rates in the literature likely reflects a lack of consistency in applying diagnostic criteria.150

Most research reports to date are limited by their cross-sectional designs,42,145,147,151,152 lack of comparison groups,42 heterogeneous samples,147 differing fatigue scales, small sample sizes,146 varying baseline survivorship definitions (ie, time since diagnosis vs time since treatment cessation), and different mean survivorship durations. These design issues make it difficult to reach conclusions about the prevalence, incidence, and duration of fatigue; the associated risk factors; and QOL. Additionally, most fatigue studies of posttreatment disease-free patients have been conducted in Caucasian, English-speaking patients with breast cancer,11,146,151 and patients who have undergone peripheral stem cell or bone marrow transplant,153,154 with few exceptions.14,16,18

The cause of posttreatment fatigue in patients who are disease-free is unclear and probably multifactorial.155 One cross-sectional comparative study investigated fatigue and physiologic biomarkers of immune system activation in 20 breast cancer survivors who were fatigued (mean, 5 years since diagnosis) and in 20 nonfatigued survivors.146 Fatigued survivors had significantly higher serum markers (interleukin-1 receptor antagonist [IL-1ra], soluble tumor necrosis factor type II, and neopterin) and lower cortisol levels when compared with nonfatigued survivors. Significantly higher numbers of circulating T lymphocytes that correlated with elevated serum IL-1ra levels also suggest that persistent fatigue in survivors may be caused by a chronic inflammatory process involving the T-cell compartment.11

Other risk factors associated with posttreatment fatigue in patients who are disease-free include pretreatment fatigue, anxiety and depression levels,156 physical activity levels,157,158 coping methods and cancer-related stressors, comorbidities, type of malignancy, prior treatment patterns, and treatment late effects. In a Norwegian study of Hodgkin disease survivors in remission for more than 5 years, higher fatigue levels were documented in those who had pulmonary dysfunction148; the prevalence of chronic fatigue was 2 to 3 times higher than in survivors without pulmonary dysfunction. No significant correlations were found between fatigue and cardiac sequelae as measured by echocardiography, exercise testing, and chest radiography.148

Prior treatment patterns may affect the fatigue. Women who had received radiation therapy had the lowest fatigue scores. Two studies testing the effects of physical activity interventions on fatigue in breast cancer survivors found that individualized, prescriptive exercise reduced fatigue. However, researchers emphasize that it is critical for exercise to be individualized to the survivor's abilities to prevent exacerbation of cancer treatment toxicities.157,158

Education and Counseling of Patient and Family

Patients who are completing treatment and their families should be educated about the pattern and level of fatigue that can be expected during this period. Although a significant subset of patients continue to experience distressing levels of fatigue that interfere with function, most patients experience a gradual decrease in fatigue and return of energy to normal levels.12,149 Regular monitoring of fatigue levels can document the decrease in fatigue that normally occurs after treatment. Health care providers should continue to screen patients regularly for fatigue during follow-up visits. Patients can benefit from general fatigue management strategies, including energy conservation and distraction. A focus on finding meaning in life should be an ongoing effort.

Nonpharmacologic Interventions

Specific interventions recommended to manage fatigue during active cancer treatment are also recommended for use in the posttreatment period in patients who are disease-free64; however, there are fewer studies of physically based therapies in posttreatment.

Physical Activity: Physical activity is a category 1 recommendation. Improving strength, energy, and fitness through regular exercise have been shown to facilitate the transition from patient to survivor, decrease anxiety and depression, improve body image, and increase tolerance for physical activity even in patients who implement a moderate walking exercise program. However, if the patient is significantly deconditioned, weak, or has relevant late effects of treatment (such as cardiopulmonary limitations), referral to a physiatrist or a supervised rehabilitation program may be indicated. Exercise should be recommended with caution in patients who have fever or remain anemic, neutropenic, or thrombocytopenic after treatment. Of the nonpharmacologic approaches for managing CRF, exercise has the best evidence to support its effectiveness.64,159163 A meta-analysis of 44 studies including 3254 cancer survivors concluded that exercise reduced fatigue, especially in programs that involved moderate-intensity resistance exercise among older cancer survivors.164 Further guidance on physical activity can be found in the NCCN Guidelines for Survivorship (to view the most recent version of these guidelines, visit NCCN.org).

Psychosocial Interventions: Psychosocial interventions, including CBT/BT, mindfulness-based stress reduction, psychoeducational therapies/educational therapies, and supportive expressive therapies are category 1 recommendations80,107,108,117,119,155,165168 (see “Interventions for Patients on Active Treatment,” page 1025).

Additional Nonpharmacologic Approaches: Nutritional consultation and CBT for sleep (category 1)112,126 may be helpful for fatigue management during posttreatment. Several published studies169171 support the conclusion that CBT interventions designed to optimize sleep quality in patients with cancer may also improve fatigue. Positive effects on both sleep and fatigue after 4 to 5 weekly BT sessions have been reported in RCTs of patients who reported chronic insomnia in the survivorship phase after cancer treatment.172174 Two smaller studies of patients with current complaints of insomnia in the survivorship phase reported improved sleep and fatigue.169,170 Two other studies found positive benefits of a behavioral intervention on sleep and fatigue that were not sustained over time.128,171 The American Academy of Sleep Medicine (AASM) has recommended 3 specific therapies for chronic insomnia in healthy individuals: relaxation training, CBT, and stimulus control therapy.175 AASM has also published clinical guidelines for the management of chronic insomnia in adults.176

Pharmacologic Interventions

If indicated, anemia, pain, and emotional distress should be treated according to the NCCN Guidelines for Supportive Care (available at NCCN.org). Treatment may also be individually optimized as necessary for sleep dysfunction, nutritional deficit or imbalance, and comorbidities.

Some evidence supports the use of psychostimulants after cancer therapy. A 54% response rate to methylphenidate has been reported in a phase II trial of 37 patients with breast cancer in remission.177 An RCT of 154 patients postchemotherapy also found an improvement in fatigue symptoms in the active arm.178 Similar to patients receiving active treatment, modafinil has limited study data in patients posttreatment. Although pilot studies suggested that modafinil may be associated with reduced fatigue,179,180 the improved outcome did not hold in larger trials140,181 (see “Interventions for Patients on Active Treatment,” page 1025). The panel agrees that methylphenidate may be considered after ruling out other causes of fatigue, but does not recommend the use of modafinil.

Interventions for Patients at the End of Life

Although the assessment and management of fatigue at the end of life parallels the general principles of this guideline, a few issues are specific to this population. Factors that have a greater likelihood of association with fatigue at the end of life include anemia, medication adverse effects and polypharmacy, cognitive impairment, adverse effects of recent treatment, and malnutrition.182 Evaluating and correcting these contributing factors could reduce fatigue severity.

It is likely that fatigue will increase substantially as the disease progresses; however, patterns of fatigue are variable. For some adults, fatigue may be characterized as constant and unrelenting; for others, it is unpredictable and may occur suddenly.41,183 At the end of life, most research has demonstrated that patients with cancer experience fatigue in the context of multiple symptoms. In a study of 278 Swedish adults admitted to a palliative care unit, 100% reported fatigue; other symptoms included pain (83%), dyspnea (77%), and appetite loss (75%).184 In a large sample of adults receiving palliative care (N=1000), Walsh et al185 noted that individuals with advanced cancer had multiple symptoms. Pain was the most prevalent (84%), followed by fatigue (69%), weakness (66%), and lack of energy (61%). Walsh and Rybicki186 cluster-analyzed 25 symptoms in 1000 consecutive admissions to a palliative care program and found 7 symptom clusters. The fatigue cluster included easy fatigue, weakness, anorexia, lack of energy, dry mouth, early satiety, weight loss, and taste changes. Given et al31,187 postulate that pain and fatigue could have a synergistic effect that worsens the overall symptom experience in elderly patients with cancer. Children with advanced cancer also experienced multiple symptoms at the end of life, most commonly fatigue, pain, and dyspnea.188

Education and Counseling of Patient and Family

Individuals with advanced cancer and their caregivers need information about the management of symptoms, including fatigue.189 This includes information about the causes, patterns, and consequences of fatigue during treatment for advanced cancer and end-of-life care.

Several major consequences of fatigue have been described, including its effect on functional status, emotional distress, and suffering. As fatigue escalates, it is likely to increasingly interfere with usual activities.183 Families need to be apprised of this issue so they can plan accordingly. Fatigue is likely to have a significant effect on emotional well-being.183,188 According to parents who cared for a child at the end of life, more than 90% of the children experienced fatigue and almost 60% experienced significant suffering from it.188 In a case study of 15 adults with advanced disease, fatigue resulted in substantial regret, sadness, and sense of loss due to the deterioration of one's health.183 Mystakidou et al190 reported that a patient's desire for hastened death was predicted by feelings of sadness, a lack of appetite, pain, and fatigue.

Given the high prevalence of fatigue and other symptoms at the end of life, symptom management needs to be a major focus of care. Active commitment by the health care team to palliative care is critical when aggressive cancer therapy is given to patients with a low likelihood of long-term survival.188 Interventions for fatigue should be initiated to relieve or diminish suffering, although it is recognized that some causes of fatigue cannot be assuaged.64

General Strategies for Management of Fatigue

Energy conservation is a self-care strategy for individuals with advanced cancer and their caregivers.66 The goal of energy conservation is to maintain a balance between rest and activity during times of high fatigue so that valued activities can be maintained. Energy conservation strategies include setting priorities and realistic expectations, delegating activities of lesser importance, eliminating nonessential activities, pacing oneself, taking extra rest periods, and planning high-energy activities at times of peak energy. It may also include the use of assistive devices and labor-saving techniques. Distraction may also be helpful. Patients receiving palliative care should be allowed daytime naps as long as they do not disturb nighttime sleep. In a situation of escalating fatigue at the end of life, family members may wish to designate individuals to assume activities relinquished by the individual with cancer.

Nonpharmacologic Interventions

Although there is no category 1 evidence for nonpharmacologic interventions at the end of life, clinicians are encouraged to consider matching the patient with physical activity or psychosocial intervention as indicated. Psychosocial intervention at this stage may focus on meaning and dignity, and gaining acceptance of the limitations imposed by fatigue. It may include a reemphasis on meaningful family interactions that do not require high-level physical activity.191 Sustaining a sense of meaning has been demonstrated to allow patients with cancer to endorse a high QOL despite significant symptoms.192 Studies suggest that interventions aimed at sustaining or enhancing meaning and/or dignity can significantly reduce distress related to symptoms and improve overall QOL.193195

Although fatigue may increase at end of life, some individuals may choose to be active despite failing health. Some evidence shows that exercise is beneficial to individuals with incurable cancer and a short life expectancy. A group exercise program was evaluated in a pilot study of 63 Norwegian outpatients receiving palliative care.196 The program consisted of two 50-minute sessions twice a week for 6 weeks that combined strength building, standing balance, and aerobic exercise. The exercise participants had less physical fatigue and increased walking distance. There were no adverse effects of exercise, although 29 of the 63 participants did not complete the program due to sudden death, or for medical and social reasons.

A small pilot study was conducted to evaluate an exercise program for 9 individuals with advanced cancer enrolled in a home hospice program.197 A physical therapist guided participants in the selection of several activities (eg, walking, arm exercises with resistance, marching in place, dancing). These were performed at different times throughout the day on a schedule devised jointly by the therapist and participant. All participants were able to increase their activity level over a 2-week period without increased fatigue. A trend was seen toward increased QOL and decreased anxiety. Although more research is needed, enhanced activity shows promise as a fatigue management strategy at the end of life; psychosocial interventions, sleep therapy, family interaction, and nutritional therapy are also helpful.

Reports of fatigue from 82 men with locally advanced or metastatic prostate cancer who underwent a 12-week exercise program was compared with those from a wait-list control group (N=73). The men in the exercise group reported less interference of fatigue with daily activities and better QOL. They also demonstrated better upper and lower body muscle fitness. Body composition was not affected.

Based on a systematic review of 20 exercise studies relevant to fatigue and muscle wasting in multiple myeloma, Strong et al198 summarized weight-bearing precautions for bone metastases and exercise guidelines for adults with solid tumors and hematologic cancers, older cancer survivors, and individuals with CRF. An exercise protocol for multiple myeloma that incorporated aerobic, resistance, and flexibility exercises was also recommended.

Pharmacologic Interventions

There continues to be interest in psychostimulant drugs for patients with cancer at the end of life, although studies have had mixed results. Methylphenidate has been shown to yield improvement in fatigue in patients with advanced cancer in 2 pilot studies.199,200 However, 2 RCTs reported an improvement in fatigue in both the methylphenidate and placebo arms.201,202 Another psychostimulant, dexamphetamine (10 mg twice daily for 8 days), was evaluated for fatigue in patients with advanced cancer.203 The results of an RCT showed tolerance of the drug and short-term improvement in fatigue on the second day, but no long-term benefit by the end of the 8-day study. A recent RCT in patients with advanced non–small cell lung cancer (n=160) showed no significant improvement between patients treated with modafinil (n=75) versus placebo (n=85). Although well-tolerated, the mean score change between groups as measured by the FACT-F scale was not significant (0.20; 95% CI, −3.56 to 3.97).181 Overall, methylphenidate may be considered with caution for selected terminal patients.

Evidence supports the effectiveness of corticosteroids (prednisone and its derivative, and dexamethasone) in providing short-term relief for fatigue and improving QOL.204207 An RCT in patients with advanced cancer demonstrated significant improvement of fatigue in patients receiving dexamethasone (n=43) compared with those receiving placebo (n=41) for 14 days (P=.008).208 Improved outcome was determined from the FACT-F subscale as the primary end point. An assessment of overall QOL showed improvement at day 15 (P=.03) and in physical well-being measured at day 8 (P=.007) and day 15 (P=.002), as measured by the Edmonton Symptom Assessment Scale for physical distress. This study was effective as a short-term therapy, but the long-term effects were not evaluated.208 Recently, in a second RCT investigating the effects of methylprednisone in patients with advanced cancer receiving opium, fatigue was measured in patients given 16 mg of methylprednisone twice daily (n=26) versus patients in the placebo group (n=24).209 Patients receiving methylprednisone experienced a 17-point improvement on the EORTC-QOL Questionnaire C30210 compared with the 3-point decline recorded by the placebo group (−17 vs 3 points; P=.003).209

Given the toxicity associated with long-term use, consideration of steroids is restricted to the terminally ill, patients with fatigue and concomitant anorexia, and patients with pain related to brain or bone metastases. In addition, interest has been shown in the progestational agent megestrol acetate for improving fatigue. A systematic review demonstrated the safety and efficacy of megestrol acetate in treating cachexia for patients with cancer.211 However, a second systematic review and meta-analysis of 4 studies revealed no benefit of progestational steroids compared with placebo for treatment of CRF (z score=0.78; P=.44).138,212

Treatment for sleep dysfunction, nutritional deficit, or comorbidities may be optimized to the specific needs of the patient and family along the illness trajectory, and clinicians are advised to refer to the appropriate NCCN Guidelines for Supportive Care (available at NCCN.org) for the management of pain, distress, and anemia in patients at the end of life. The NCCN Panel would like to emphasize that eating and nutrition should be tailored to the terminal patient's comfort and should not be forced on the patient, because nutritional decline is expected.

Reevaluation Phase

Because fatigue may arise at many points during the course of a patient's disease and treatment, ongoing reevaluation of the patient's status (with appropriate modifications and institution of new treatments) is an integral part of effective overall fatigue management.

Summary

The NCCN Guidelines for CRF propose a treatment algorithm in which patients are evaluated regularly for fatigue using a brief screening instrument and are treated as indicated by their fatigue level. Fatigue should be minimally evaluated with the scale outlined in the algorithm; however, there are additional tools for the measurement of fatigue that may be used to identify fatigue as appropriate (see Table 1; available online, in these guidelines, at NCCN.org [MS-23]).

Management of fatigue begins with primary oncology team members who perform the initial screening and either provide basic education and counseling or expand the initial screening to a more focused evaluation for moderate or higher levels of fatigue. The focused evaluation includes assessment of current disease and treatment status, a review of body systems, and an in-depth fatigue evaluation. In addition, the patient is assessed for the presence of treatable factors known to contribute to fatigue. If present, factors should be treated according to practice guidelines, with referral to other care professionals as appropriate, and the patient's fatigue should be reevaluated regularly. If none of the factors is present or if the fatigue is unresolved, appropriate fatigue management and treatment strategies are selected within the context of the patient's clinical status (ie, active cancer treatment, posttreatment, end-of-life care). Management of fatigue is cause-specific when conditions known to induce fatigue can be identified and treated. When specific causes of fatigue cannot be identified and corrected, nonpharmacologic and pharmacologic treatment of fatigue should be initiated.

Nonpharmacologic interventions may include a moderate exercise program to improve functional capacity and activity tolerance; psychosocial programs to manage stress and increase support; implementation of energy conservation strategies; and nutritional and sleep interventions as appropriate. Pharmacologic therapy may include drugs used to treat comorbidities, such as levothyroxine. A recent update on the use of the psychostimulant methylphenidate suggests that it may provide some benefit.213 A second agent that may be helpful for short-term use in advanced cancer is the corticosteroid methylprednisolone.208,209,214 However, potential treatment modalities in managing fatigue require further research.

Effective management of CRF involves an informed and supportive oncology care team that assesses fatigue levels regularly, counsels and educates patients regarding strategies for coping with fatigue, and uses institutional experts for referral of patients with unresolved fatigue.36 The oncology care team must recognize the many patient-, provider-, and system-related behaviors that can impede effective fatigue management. Reducing barriers by use of available resources and evidence-based guidelines increases benefits to patients experiencing fatigue.215,216

Individual Disclosures of the NCCN Cancer-Related Fatigue Panel

T1

References

  • 1.

    Ahlberg K, Ekman T, Gaston-Johansson F, Mock V. Assessment and management of cancer-related fatigue in adults. Lancet 2003;362:640650.

  • 2.

    Collins JJ, Devine TD, Dick GS et al.. The measurement of symptoms in young children with cancer: the validation of the Memorial Symptom Assessment Scale in children aged 7–12. J Pain Symptom Manage 2002;23:1016.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 3.

    Wagner LI, Cella D. Fatigue and cancer: causes, prevalence and treatment approaches. Br J Cancer 2004;91:822828.

  • 4.

    Henry DH, Viswanathan HN, Elkin EP et al.. Symptoms and treatment burden associated with cancer treatment: results from a cross-sectional national survey in the U.S. Support Care Cancer 2008;16:791801.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 5.

    Hofman M, Ryan JL, Figueroa-Moseley CD et al.. Cancer-related fatigue: the scale of the problem. Oncologist 2007;12(Suppl 1):410.

  • 6.

    Portenoy RK, Kornblith AB, Wong G et al.. Pain in ovarian cancer patients. Prevalence, characteristics, and associated symptoms. Cancer 1994;74:907915.

  • 7.

    Ventafridda V, De Conno F, Ripamonti C et al.. Quality-of-life assessment during a palliative care programme. Ann Oncol 1990;1:415420.

  • 8.

    Curtis EB, Krech R, Walsh TD. Common symptoms in patients with advanced cancer. J Palliat Care 1991;7:2529.

  • 9.

    Portenoy RK, Thaler HT, Kornblith AB et al.. Symptom prevalence, characteristics and distress in a cancer population. Qual Life Res 1994;3:183189.

  • 10.

    Wang XS, Zhao F, Fisch MJ et al.. Prevalence and characteristics of moderate to severe fatigue: a multicenter study in cancer patients and survivors. Cancer 2014;120:425432.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 11.

    Bower JE, Ganz PA, Aziz N et al.. T-cell homeostasis in breast cancer survivors with persistent fatigue. J Natl Cancer Inst 2003;95:11651168.

  • 12.

    Bower JE, Ganz PA, Desmond KA et al.. Fatigue in breast cancer survivors: occurrence, correlates, and impact on quality of life. J Clin Oncol 2000;18:743753.

  • 13.

    Crom DB, Hinds PS, Gattuso JS et al.. Creating the basis for a breast health program for female survivors of Hodgkin disease using a participatory research approach. Oncol Nurs Forum 2005;32:11311141.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 14.

    Fossa SD, Dahl AA, Loge JH. Fatigue, anxiety, and depression in long-term survivors of testicular cancer. J Clin Oncol 2003;21:12491254.

  • 15.

    Haghighat S, Akbari ME, Holakouei K et al.. Factors predicting fatigue in breast cancer patients. Support Care Cancer 2003;11:533538.

  • 16.

    Ruffer JU, Flechtner H, Tralls P et al.. Fatigue in long-term survivors of Hodgkin's lymphoma; a report from the German Hodgkin Lymphoma Study Group (GHSG). Eur J Cancer 2003;39:21792186.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 17.

    Servaes P, Verhagen S, Bleijenberg G. Determinants of chronic fatigue in disease-free breast cancer patients: a cross-sectional study. Ann Oncol 2002;13:589598.

  • 18.

    Servaes P, Verhagen S, Schreuder HW et al.. Fatigue after treatment for malignant and benign bone and soft tissue tumors. J Pain Symptom Manage 2003;26:11131122.

  • 19.

    Olson K. A new way of thinking about fatigue: a reconceptualization. Oncol Nurs Forum 2007;34:9399.

  • 20.

    Olson K, Krawchuk A, Quddusi T. Fatigue in individuals with advanced cancer in active treatment and palliative settings. Cancer Nurs 2007;30:E110.

  • 21.

    Hinds PS, Quargnenti A, Bush AJ et al.. An evaluation of the impact of a self-care coping intervention on psychological and clinical outcomes in adolescents with newly diagnosed cancer. Eur J Oncol Nurs 2000;4:6e–17; discussion 18–19.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 22.

    Janda M, Gerstner N, Obermair A et al.. Quality of life changes during conformal radiation therapy for prostate carcinoma. Cancer 2000;89:13221328.

  • 23.

    Morrow GR, Andrews PL, Hickok JT et al.. Fatigue associated with cancer and its treatment. Support Care Cancer 2002;10:389398.

  • 24.

    Bower JE. Cancer-related fatigue: links with inflammation in cancer patients and survivors. Brain Behav Immun 2007;21:863871.

  • 25.

    Schubert C, Hong S, Natarajan L et al.. The association between fatigue and inflammatory marker levels in cancer patients: a quantitative review. Brain Behav Immun 2007;21:413427.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 26.

    Miller AH, Ancoli-Israel S, Bower JE et al.. Neuroendocrine-immune mechanisms of behavioral comorbidities in patients with cancer. J Clin Oncol 2008;26:971982.

  • 27.

    Berger AM, Wielgus K, Hertzog M et al.. Patterns of circadian activity rhythms and their relationships with fatigue and anxiety/depression in women treated with breast cancer adjuvant chemotherapy. Support Care Cancer 2010;18:105114.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 28.

    al-Majid S, McCarthy DO. Cancer-induced fatigue and skeletal muscle wasting: the role of exercise. Biol Res Nurs 2001;2:186197.

  • 29.

    Rich TA. Symptom clusters in cancer patients and their relation to EGFR ligand modulation of the circadian axis. J Support Oncol 2007;5:167174; discussion 176–167.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 30.

    Mock V, Atkinson A, Barsevick A et al.. NCCN Practice Guidelines for Cancer-Related Fatigue. Oncology (Williston Park) 2000;14:151161.

  • 31.

    Given CW, Given B, Azzouz F et al.. Comparison of changes in physical functioning of elderly patients with new diagnoses of cancer. Med Care 2000;38:482493.

  • 32.

    Given B, Given CW, McCorkle R et al.. Pain and fatigue management: results of a nursing randomized clinical trial. Oncol Nurs Forum 2002;29:949956.

  • 33.

    Mock V, McCorkle R, Ropka ME. Fatigue and physical functioning during breast cancer treatment. Oncol Nurs Forum 2002;29:338.

  • 34.

    Nail LM. Fatigue in patients with cancer. Oncol Nurs Forum 2002;29:537.

  • 35.

    Malik UR, Makower DF, Wadler S. Interferon-mediated fatigue. Cancer 2001;92:16641668.

  • 36.

    Escalante CP, Grover T, Johnson BA et al.. A fatigue clinic in a comprehensive cancer center: design and experiences. Cancer 2001;92:17081713.

  • 37.

    Hinds PS, Hockenberry M, Tong X et al.. Validity and reliability of a new instrument to measure cancer-related fatigue in adolescents. J Pain Symptom Manage 2007;34:607618.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 38.

    Hockenberry MJ, Hinds PS, Barrera P et al.. Three instruments to assess fatigue in children with cancer: the child, parent and staff perspectives. J Pain Symptom Manage 2003;25:319328.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 39.

    Varni JW, Burwinkle TM, Katz ER et al.. The PedsQL in pediatric cancer: reliability and validity of the Pediatric Quality of Life Inventory Generic Core Scales, Multidimensional Fatigue Scale, and Cancer Module. Cancer 2002;94:20902106.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 40.

    Grant M. Fatigue and quality of life with cancer. In: Winningham ML, Barton-Burke M, eds. Fatigue in Cancer: A Multidimensional Approach. Sudbury, MA: Jones & Bartlett; 2000:353364.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 41.

    Barsevick AM, Whitmer K, Walker L. In their own words: using the common sense model to analyze patient descriptions of cancer-related fatigue. Oncol Nurs Forum 2001;28:13631369.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 42.

    Curt GA, Breitbart W, Cella D et al.. Impact of cancer-related fatigue on the lives of patients: new findings from the Fatigue Coalition. Oncologist 2000;5:353360.

  • 43.

    Holley S. Cancer-related fatigue. Suffering a different fatigue. Cancer Pract 2000;8:8795.

  • 44.

    Mendoza TR, Wang XS, Cleeland CS et al.. The rapid assessment of fatigue severity in cancer patients: use of the Brief Fatigue Inventory. Cancer 1999;85:11861196.

  • 45.

    Given BA, Given CW, Kozachik S. Family support in advanced cancer. CA Cancer J Clin 2001;51:213231.

  • 46.

    Luciani A, Jacobsen PB, Extermann M et al.. Fatigue and functional dependence in older cancer patients. Am J Clin Oncol 2008;31:424430.

  • 47.

    van Ryn M, Sanders S, Kahn K et al.. Objective burden, resources, and other stressors among informal cancer caregivers: a hidden quality issue? Psychooncology 2011;20:4452.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 48.

    Ancoli-Israel S, Moore PJ, Jones V. The relationship between fatigue and sleep in cancer patients: a review. Eur J Cancer Care (Engl) 2001;10:245255.

  • 49.

    Berger AM, Walker SN. An explanatory model of fatigue in women receiving adjuvant breast cancer chemotherapy. Nurs Res 2001;50:4252.

  • 50.

    Dodd MJ, Miaskowski C, Paul SM. Symptom clusters and their effect on the functional status of patients with cancer. Oncol Nurs Forum 2001;28:465470.

  • 51.

    Hinds PS, Hockenberry M, Rai SN et al.. Nocturnal awakenings, sleep environment interruptions, and fatigue in hospitalized children with cancer. Oncol Nurs Forum 2007;34:393402.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 52.

    de Raaf PJ, de Klerk C, Timman R et al.. Systematic monitoring and treatment of physical symptoms to alleviate fatigue in patients with advanced cancer: a randomized controlled trial. J Clin Oncol 2013;31:716723.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 53.

    Hopwood P, Stephens RJ. Depression in patients with lung cancer: prevalence and risk factors derived from quality-of-life data. J Clin Oncol 2000;18:893903.

  • 54.

    Loge JH, Abrahamsen AF, Ekeberg, Kaasa S. Fatigue and psychiatric morbidity among Hodgkin's disease survivors. J Pain Symptom Manage 2000;19:9199.

  • 55.

    Savard J, Morin CM. Insomnia in the context of cancer: a review of a neglected problem. J Clin Oncol 2001;19:895908.

  • 56.

    Berger AM, Mitchell SA. Modifying cancer-related fatigue by optimizing sleep quality. J Natl Compr Canc Netw 2008;6:313.

  • 57.

    Roscoe JA, Kaufman ME, Matteson-Rusby SE et al.. Cancer-related fatigue and sleep disorders. Oncologist 2007;12(Suppl 1):3542.

  • 58.

    Berger AM, Parker KP, Young-McCaughan S et al.. Sleep wake disturbances in people with cancer and their caregivers: state of the science. Oncol Nurs Forum 2005;32:E98126.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 59.

    Palesh OG, Collie K, Batiuchok D et al.. A longitudinal study of depression, pain, and stress as predictors of sleep disturbance among women with metastatic breast cancer. Biol Psychol 2007;75:3744.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 60.

    Mock V, Frangakis C, Davidson NE et al.. Exercise manages fatigue during breast cancer treatment: a randomized controlled trial. Psychooncology 2005;14:464477.

  • 61.

    Schwartz AL. Daily fatigue patterns and effect of exercise in women with breast cancer. Cancer Pract 2000;8:1624.

  • 62.

    Canaris GJ, Manowitz NR, Mayor G, Ridgway EC. The Colorado thyroid disease prevalence study. Arch Intern Med 2000;160:526534.

  • 63.

    Strasser F, Palmer JL, Schover LR et al.. The impact of hypogonadism and autonomic dysfunction on fatigue, emotional function, and sexual desire in male patients with advanced cancer: a pilot study. Cancer 2006;107:29492957.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 64.

    Mitchell SA, Beck SL, Hood LE et al.. Putting evidence into practice: evidence-based interventions for fatigue during and following cancer and its treatment. Clin J Oncol Nurs 2007;11:99113.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 65.

    Barsevick AM, Whitmer K, Sweeney C, Nail LM. A pilot study examining energy conservation for cancer treatment-related fatigue. Cancer Nurs 2002;25:333341.

  • 66.

    Barsevick AM, Dudley W, Beck S et al.. A randomized clinical trial of energy conservation for patients with cancer-related fatigue. Cancer 2004;100:13021310.

  • 67.

    Mustian KM, Morrow GR, Carroll JK et al.. Integrative nonpharmacologic behavioral interventions for the management of cancer-related fatigue. Oncologist 2007;12(Suppl 1):5267.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 68.

    Mitchell SA, Hoffman AJ, Clark JC et al.. Putting evidence into practice: an update of evidence-based interventions for cancer-related fatigue during and following treatment. Clin J Oncol Nurs 2014;18(Suppl):3858.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 69.

    Oncology Nursing Society Putting Evidence into Practice (PEP). Fatigue. Available at: https://www.ons.org/practice-resources/pep. Accessed April 24, 2015.

  • 70.

    Irwin M, Johnson LA, eds. Putting Evidence Into Practice: A Pocket Guide to Cancer Symptom Management. Pittsburgh, PA: Oncology Nursing Society; 2014.

  • 71.

    Bower JE, Bak K, Berger A et al.. Screening, assessment, and management of fatigue in adult survivors of cancer: an American Society of Clinical oncology clinical practice guideline adaptation. J Clin Oncol 2014;32:18401850.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 72.

    Howell D, Keller-Olaman S, Oliver TK et al.. A pan-Canadian practice guideline and algorithm: screening, assessment, and supportive care of adults with cancer-related fatigue. Curr Oncol 2013;20:e233246.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 73.

    Mustian K, Palesh OG, Heckler CE et al.. Cancer-related fatigue interferes with activities of daily living among 753 patients receiving chemotherapy: a URCC CCOP study [abstract]. J Clin Oncol 2008;26(Suppl):Abstract 9500.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 74.

    Puetz TW, Herring MP. Differential effects of exercise on cancer-related fatigue during and following treatment: a meta-analysis. Am J Prev Med 2012;43:e124.

  • 75.

    Mishra SI, Scherer RW, Snyder C et al.. Exercise interventions on health-related quality of life for people with cancer during active treatment. Cochrane Database Syst Rev 2012;8:CD008465.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 76.

    Gardner JR, Livingston PM, Fraser SF. Effects of exercise on treatment-related adverse effects for patients with prostate cancer receiving androgen-deprivation therapy: a systematic review. J Clin Oncol 2014;32:335346.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 77.

    Vermaete N, Wolter P, Verhoef G, Gosselink R. Physical activity, physical fitness and the effect of exercise training interventions in lymphoma patients: a systematic review. Ann Hematol 2013;92:10071021.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 78.

    van Haren IE, Timmerman H, Potting CM et al.. Physical exercise for patients undergoing hematopoietic stem cell transplantation: systematic review and meta-analyses of randomized controlled trials. Phys Ther 2013;93:514528.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 79.

    Cramp F, Daniel J. Exercise for the management of cancer-related fatigue in adults. Cochrane Database Syst Rev 2008:CD006145.

  • 80.

    Duijts SF, Faber MM, Oldenburg HS et al.. Effectiveness of behavioral techniques and physical exercise on psychosocial functioning and health-related quality of life in breast cancer patients and survivors—a meta-analysis. Psychooncology 2011;20:115126.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 81.

    Kangas M, Bovbjerg DH, Montgomery GH. Cancer-related fatigue: a systematic and meta-analytic review of non-pharmacological therapies for cancer patients. Psychol Bull 2008;134:700741.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 82.

    McMillan EM, Newhouse IJ. Exercise is an effective treatment modality for reducing cancer-related fatigue and improving physical capacity in cancer patients and survivors: a meta-analysis. Appl Physiol Nutr Metab 2011;36:892903.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 83.

    Velthuis MJ, Agasi-Idenburg SC, Aufdemkampe G, Wittink HM. The effect of physical exercise on cancer-related fatigue during cancer treatment: a meta-analysis of randomised controlled trials. Clin Oncol (R Coll Radiol) 2010;22:208221.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 84.

    U.S. Department of Health & Human Services. Physical Activity Guidelines for Americans. 2008. Available at: http://www.health.gov/paguidelines/. Accessed April 24, 2015.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 85.

    Courneya KS, Friedenreich CM, Sela RA et al.. The group psychotherapy and home-based physical exercise (group-hope) trial in cancer survivors: physical fitness and quality of life outcomes. Psychooncology 2003;12:357374.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 86.

    Courneya KS, Mackey JR, Bell GJ et al.. Randomized controlled trial of exercise training in postmenopausal breast cancer survivors: cardiopulmonary and quality of life outcomes. J Clin Oncol 2003;21:16601668.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 87.

    Drouin JS, Armstrong H, Krause S. Effects of aerobic exercise training on peak aerobic capacity, fatigue, and psychological factors during radiation for breast cancer. Rehab Oncol 2005;23:1117.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 88.

    Schwartz AL, Mori M, Gao R et al.. Exercise reduces daily fatigue in women with breast cancer receiving chemotherapy. Med Sci Sports Exerc 2001;33:718723.

  • 89.

    Segal RJ, Reid RD, Courneya KS et al.. Resistance exercise in men receiving androgen deprivation therapy for prostate cancer. J Clin Oncol 2003;21:16531659.

  • 90.

    Schmitz KH, Courneya KS, Matthews C et al.. American College of Sports Medicine roundtable on exercise guidelines for cancer survivors. Med Sci Sports Exerc 2010;42:14091426.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 91.

    Sood A, Barton DL, Bauer BA, Loprinzi CL. A critical review of complementary therapies for cancer-related fatigue. Integr Cancer Ther 2007;6:813.

  • 92.

    Balk J, Day R, Rosenzweig M, Beriwal S. Pilot, randomized, modified, double-blind, placebo-controlled trial of acupuncture for cancer-related fatigue. J Soc Integr Oncol 2009;7:411.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 93.

    Mao JJ, Styles T, Cheville A et al.. Acupuncture for nonpalliative radiation therapy-related fatigue: feasibility study. J Soc Integr Oncol 2009;7:5258.

  • 94.

    Molassiotis A, Sylt P, Diggins H. The management of cancer-related fatigue after chemotherapy with acupuncture and acupressure: a randomised controlled trial. Complement Ther Med 2007;15:228237.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 95.

    Vickers AJ, Straus DJ, Fearon B, Cassileth BR. Acupuncture for postchemotherapy fatigue: a phase II study. J Clin Oncol 2004;22:17311735.

  • 96.

    Post-White J, Kinney ME, Savik K et al.. Therapeutic massage and healing touch improve symptoms in cancer. Integr Cancer Ther 2003;2:332344.

  • 97.

    Cassileth BR, Vickers AJ. Massage therapy for symptom control: outcome study at a major cancer center. J Pain Symptom Manage 2004;28:244249.

  • 98.

    Towler P, Molassiotis A, Brearley SG. What is the evidence for the use of acupuncture as an intervention for symptom management in cancer supportive and palliative care: an integrative overview of reviews. Support Care Cancer 2013;21:29132923.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 99.

    Posadzki P, Moon TW, Choi TY et al.. Acupuncture for cancer-related fatigue: a systematic review of randomized clinical trials. Support Care Cancer 2013;21:20672073.

  • 100.

    Ahles TA, Tope DM, Pinkson B et al.. Massage therapy for patients undergoing autologous bone marrow transplantation. J Pain Symptom Manage 1999;18:157163.

  • 101.

    Bower JE, Garet D, Sternlieb B et al.. Yoga for persistent fatigue in breast cancer survivors: a randomized controlled trial. Cancer 2012;118:37663775.

  • 102.

    Buffart LM, van Uffelen JG, Riphagen II et al.. Physical and psychosocial benefits of yoga in cancer patients and survivors, a systematic review and meta-analysis of randomized controlled trials. BMC Cancer 2012;12:559.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 103.

    Chandwani KD, Perkins G, Nagendra HR et al.. Randomized, controlled trial of yoga in women with breast cancer undergoing radiotherapy. J Clin Oncol 2014;32:10581065.

  • 104.

    Kiecolt-Glaser JK, Bennett JM, Andridge R et al.. Yoga's impact on inflammation, mood, and fatigue in breast cancer survivors: a randomized controlled trial. J Clin Oncol 2014;32:10401049.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 105.

    Sprod LK, Fernandez ID, Janelsins MC et al.. Effects of yoga on cancer-related fatigue and global side-effect burden in older cancer survivors. J Geriatr Oncol 2015;6:814.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 106.

    Carlson LE, Garland SN. Impact of mindfulness-based stress reduction (MBSR) on sleep, mood, stress and fatigue symptoms in cancer outpatients. Int J Behav Med 2005;12:278285.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 107.

    Lengacher CA, Reich RR, Post-White J et al.. Mindfulness based stress reduction in post-treatment breast cancer patients: an examination of symptoms and symptom clusters. J Behav Med 2012;35:8694.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 108.

    Hoffman CJ, Ersser SJ, Hopkinson JB et al.. Effectiveness of mindfulness-based stress reduction in mood, breast- and endocrine-related quality of life, and well-being in stage 0 to III breast cancer: a randomized, controlled trial. J Clin Oncol 2012;30:13351342.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 109.

    Stark D, Kiely M, Smith A et al.. Anxiety disorders in cancer patients: their nature, associations, and relation to quality of life. J Clin Oncol 2002;20:31373148.

  • 110.

    Goedendorp MM, Gielissen MF, Verhagen CA, Bleijenberg G. Psychosocial interventions for reducing fatigue during cancer treatment in adults. Cochrane Database Syst Rev 2009:CD006953.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 111.

    Jacobsen PB, Donovan KA, Vadaparampil ST, Small BJ. Systematic review and meta-analysis of psychological and activity-based interventions for cancer-related fatigue. Health Psychol 2007;26:660667.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 112.

    Eaton LH, Tipton JM, eds. Oncology Nursing Society Putting Evidence into Practice: Improving oncology patient outcomes. Pittsburgh, PA: Oncology Nursing Society; 2009.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 113.

    Jacobsen PB, Meade CD, Stein KD et al.. Efficacy and costs of two forms of stress management training for cancer patients undergoing chemotherapy. J Clin Oncol 2002;20:28512862.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 114.

    Armes J, Chalder T, Addington-Hall J et al.. A randomized controlled trial to evaluate the effectiveness of a brief, behaviorally oriented intervention for cancer-related fatigue. Cancer 2007;110:13851395.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 115.

    Luebbert K, Dahme B, Hasenbring M. The effectiveness of relaxation training in reducing treatment-related symptoms and improving emotional adjustment in acute non-surgical cancer treatment: a meta-analytical review. Psychooncology 2001;10:490502.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 116.

    Montgomery GH, Kangas M, David D et al.. Fatigue during breast cancer radiotherapy: an initial randomized study of cognitive-behavioral therapy plus hypnosis. Health Psychol 2009;28:317322.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 117.

    Boesen EH, Ross L, Frederiksen K et al.. Psychoeducational intervention for patients with cutaneous malignant melanoma: a replication study. J Clin Oncol 2005;23:12701277.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 118.

    Gaston-Johansson F, Fall-Dickson JM, Nanda J et al.. The effectiveness of the comprehensive coping strategy program on clinical outcomes in breast cancer autologous bone marrow transplantation. Cancer Nurs 2000;23:277285.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 119.

    Lindemalm C, Strang P, Lekander M. Support group for cancer patients. Does it improve their physical and psychological wellbeing? A pilot study. Support Care Cancer 2005;13:652657.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 120.

    Ream E, Richardson A, Alexander-Dann C. Supportive intervention for fatigue in patients undergoing chemotherapy: a randomized controlled trial. J Pain Symptom Manage 2006;31:148161.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 121.

    Yates P, Aranda S, Hargraves M et al.. Randomized controlled trial of an educational intervention for managing fatigue in women receiving adjuvant chemotherapy for early-stage breast cancer. J Clin Oncol 2005;23:60276036.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 122.

    Allison PJ, Edgar L, Nicolau B et al.. Results of a feasibility study for a psycho-educational intervention in head and neck cancer. Psychooncology 2004;13:482485.

  • 123.

    Godino C, Jodar L, Duran A et al.. Nursing education as an intervention to decrease fatigue perception in oncology patients. Eur J Oncol Nurs 2006;10:150155.

  • 124.

    Yun YH, Lee KS, Kim YW et al.. Web-based tailored education program for disease-free cancer survivors with cancer-related fatigue: a randomized controlled trial. J Clin Oncol 2012;30:12961303.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 125.

    Brown JK. A systematic review of the evidence on symptom management of cancer-related anorexia and cachexia. Oncol Nurs Forum 2002;29:517532.

  • 126.

    Page MS, Berger AM, Johnson LB. Putting evidence into practice: evidence-based interventions for sleep-wake disturbances. Clin J Oncol Nurs 2006;10:753767.

  • 127.

    Morin C, Espie C. Insomnia: A Clinical Guide to Assessment and Treatment. New York: Kluwer Academic; 2003.

  • 128.

    Berger AM, VonEssen S, Khun BR et al.. Feasibilty of a sleep intervention during adjuvant breast cancer chemotherapy. Oncol Nurs Forum 2002;29:14311441.

  • 129.

    Food and Drug Administration. FDA News (March 14, 2007). Available at: http://www.fda.gov/NewsEvents/Newsroom/PressAnnouncements/2007/ucm108868.htm. Accessed April 24, 2015.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 130.

    National Cancer Institute. Sleep Disorders PDQ (Health Professional Version). 2010. Available at: http://www.cancer.gov/cancertopics/pdq/supportivecare/sleepdisorders/HealthProfessional. Accessed April 24, 2015.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 131.

    de la Cruz M, Hui D, Parsons HA, Bruera E. Placebo and nocebo effects in randomized double-blind clinical trials of agents for the therapy for fatigue in patients with advanced cancer. Cancer 2010;116:766774.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 132.

    Morrow GR, Hickok JT, Roscoe JA et al.. Differential effects of paroxetine on fatigue and depression: a randomized, double-blind trial from the University of Rochester Cancer Center Community Clinical Oncology Program. J Clin Oncol 2003;21:46354641.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 133.

    Roscoe JA, Morrow GR, Hickok JT et al.. Effect of paroxetine hydrochloride (Paxil) on fatigue and depression in breast cancer patients receiving chemotherapy. Breast Cancer Res Treat 2005;89:243249.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 134.

    Schwartz AL, Thompson JA, Masood N. Interferon-induced fatigue in patients with melanoma: a pilot study of exercise and methylphenidate. Oncol Nurs Forum 2002;29:E8590.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 135.

    Butler JM Jr, Case LD, Atkins J et al.. A phase III, double-blind, placebo-controlled prospective randomized clinical trial of d-threo-methylphenidate HCl in brain tumor patients receiving radiation therapy. Int J Radiat Oncol Biol Phys 2007;69:14961501.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 136.

    Mar Fan HG, Clemons M, Xu W et al.. A randomised, placebo-controlled, double-blind trial of the effects of d-methylphenidate on fatigue and cognitive dysfunction in women undergoing adjuvant chemotherapy for breast cancer. Support Care Cancer 2008;16:577583.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 137.

    Moraska AR, Sood A, Dakhil SR et al.. Phase III, randomized, double-blind, placebo-controlled study of long-acting methylphenidate for cancer-related fatigue: North Central Cancer Treatment Group NCCTG-N05C7 trial. J Clin Oncol 2010;28:36733679.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 138.

    Minton O, Richardson A, Sharpe M et al.. Drug therapy for the management of cancer-related fatigue. Cochrane Database Syst Rev 2010;7:CD006704.

  • 139.

    Jean-Pierre P, Morrow GR, Roscoe JA et al.. A phase 3 randomized, placebo-controlled, double-blind, clinical trial of the effect of modafinil on cancer-related fatigue among 631 patients receiving chemotherapy: a University of Rochester Cancer Center Community Clinical Oncology Program Research base study. Cancer 2010;116:35133520.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 140.

    Hovey E, de Souza P, Marx G et al.. Phase III, randomized, double-blind, placebo-controlled study of modafinil for fatigue in patients treated with docetaxel-based chemotherapy. Support Care Cancer 2014;22:12331242.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 141.

    Lesser GJ, Case D, Stark N et al.. A randomized, double-blind, placebo-controlled study of oral coenzyme Q10 to relieve self-reported treatment-related fatigue in newly diagnosed patients with breast cancer. J Support Oncol 2013;11:3142.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 142.

    Cruciani RA, Dvorkin E, Homel P et al.. L-carnitine supplementation in patients with advanced cancer and carnitine deficiency: a double-blind, placebo-controlled study. J Pain Symptom Manage 2009;37:622631.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 143.

    Barton DL, Liu H, Dakhil SR et al.. Wisconsin Ginseng (Panax quinquefolius) to improve cancer-related fatigue: a randomized, double-blind trial, N07C2. J Natl Cancer Inst 2013;105:12301238.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 144.

    Siegel RL, Miller KD, Jemal A. Cancer statistics, 2015. CA Cancer J Clin 2015;65:529.

  • 145.

    Knobel H, Loge JH, Nordoy T et al.. High level of fatigue in lymphoma patients treated with high dose therapy. J Pain Symptom Manage 2000;19:446456.

  • 146.

    Bower JE, Ganz PA, Aziz N, Fahey JL. Fatigue and proinflammatory cytokine activity in breast cancer survivors. Psychosom Med 2002;64:604611.

  • 147.

    Cella D, Davis K, Breitbart W et al.. Cancer-related fatigue: prevalence of proposed diagnostic criteria in a United States sample of cancer survivors. J Clin Oncol 2001;19:33853391.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 148.

    Knobel H, Havard Loge J, Lund MB et al.. Late medical complications and fatigue in Hodgkin's disease survivors. J Clin Oncol 2001;19:32263233.

  • 149.

    Stewart DE, Wong F, Duff S et al.. “What doesn't kill you makes you stronger”: an ovarian cancer survivor survey. Gynecol Oncol 2001;83:537542.

  • 150.

    Donovan KA, McGinty HL, Jacobsen PB. A systematic review of research using the diagnostic criteria for cancer-related fatigue. Psychooncology 2013;22:737744.

  • 151.

    Servaes P, Prins J, Verhagen S, Bleijenberg G. Fatigue after breast cancer and in chronic fatigue syndrome: similarities and differences. J Psychosom Res 2002;52:453459.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 152.

    Stone P, Richardson A, Ream E et al.. Cancer-related fatigue: inevitable, unimportant and untreatable? Results of a multi-centre patient survey. Cancer Fatigue Forum. Ann Oncol 2000;11:971975.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 153.

    Hann DM, Jacobsen PB, Martin SC et al.. Fatigue in women treated with bone marrow transplantation for breast cancer: a comparison with women with no history of cancer. Support Care Cancer 1997;5:4452.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 154.

    Mock V, Cameron L, Tompkins C. Every Step Counts: A Walking Exercise Program for Persons Living With Cancer. Baltimore, MD: Johns Hopkins University; 1997.

  • 155.

    Gielissen MF, Verhagen S, Witjes F, Bleijenberg G. Effects of cognitive behavior therapy in severely fatigued disease-free cancer patients compared with patients waiting for cognitive behavior therapy: a randomized controlled trial. J Clin Oncol 2006;24:48824887.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 156.

    Geinitz H, Zimmermann FB, Thamm R et al.. Fatigue in patients with adjuvant radiation therapy for breast cancer: long-term follow-up. J Cancer Res Clin Oncol 2004;130:327333.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 157.

    Schneider CM, Hsieh CC, Sprod LK et al.. Effects of supervised exercise training on cardiopulmonary function and fatigue in breast cancer survivors during and after treatment. Cancer 2007;110:918925.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 158.

    Vallance JK, Courneya KS, Plotnikoff RC et al.. Randomized controlled trial of the effects of print materials and step pedometers on physical activity and quality of life in breast cancer survivors. J Clin Oncol 2007;25:23522359.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 159.

    Conn VS, Hafdahl AR, Porock DC et al.. A meta-analysis of exercise interventions among people treated for cancer. Support Care Cancer 2006;14:699712.

  • 160.

    Knols R, Aaronson NK, Uebelhart D et al.. Physical exercise in cancer patients during and after medical treatment: a systematic review of randomized and controlled clinical trials. J Clin Oncol 2005;23:38303842.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 161.

    McNeely ML, Campbell KL, Rowe BH et al.. Effects of exercise on breast cancer patients and survivors: a systematic review and meta-analysis. CMAJ 2006;175:3441.

  • 162.

    Stricker CT, Drake D, Hoyer KA, Mock V. Evidence-based practice for fatigue management in adults with cancer: exercise as an intervention. Oncol Nurs Forum 2004;31:963976.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 163.

    Cantarero-Villanueva I, Fernandez-Lao C, Cuesta-Vargas AI et al.. The effectiveness of a deep water aquatic exercise program in cancer-related fatigue in breast cancer survivors: a randomized controlled trial. Arch Phys Med Rehabil 2013;94:221230.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 164.

    Brown JC, Huedo-Medina TB, Pescatello LS et al.. Efficacy of exercise interventions in modulating cancer-related fatigue among adult cancer survivors: a meta-analysis. Cancer Epidemiol Biomarkers Prev 2011;20:123133.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 165.

    Dolbeault S, Cayrou S, Bredart A et al.. The effectiveness of a psycho-educational group after early-stage breast cancer treatment: results of a randomized French study. Psychooncology 2009;18:647656.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 166.

    Soares A, Biasoli I, Scheliga A et al.. Association of social network and social support with health-related quality of life and fatigue in long-term survivors of Hodgkin lymphoma. Support Care Cancer 2013;21:21532159.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 167.

    Garssen B, Boomsma MF, Meezenbroek Ede J et al.. Stress management training for breast cancer surgery patients. Psychooncology 2013;22:572580.

  • 168.

    Reif K, de Vries U, Petermann F, Gorres S. A patient education program is effective in reducing cancer-related fatigue: a multi-centre randomised two-group waiting-list controlled intervention trial. Eur J Oncol Nurs 2013;17:204213.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 169.

    Davidson JR, Waisberg JL, Brundage MD, MacLean AW. Nonpharmacologic group treatment of insomnia: a preliminary study with cancer survivors. Psychooncology 2001;10:389397.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 170.

    Quesnel C, Savard J, Simard S et al.. Efficacy of cognitive-behavioral therapy for insomnia in women treated for nonmetastatic breast cancer. J Consult Clin Psychol 2003;71:189200.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 171.

    Savard J, Simard S, Ivers H, Morin CM. Randomized study on the efficacy of cognitive-behavioral therapy for insomnia secondary to breast cancer, part I: sleep and psychological effects. J Clin Oncol 2005;23:60836096.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 172.

    Dirksen SR, Epstein DR. Efficacy of an insomnia intervention on fatigue, mood and quality of life in breast cancer survivors. J Adv Nurs 2008;61:664675.

  • 173.

    Epstein DR, Dirksen SR. Randomized trial of a cognitive-behavioral intervention for insomnia in breast cancer survivors. Oncol Nurs Forum 2007;34:E5159.

  • 174.

    Espie CA, Fleming L, Cassidy J et al.. Randomized controlled clinical effectiveness trial of cognitive behavior therapy compared with treatment as usual for persistent insomnia in patients with cancer. J Clin Oncol 2008;26:46514658.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 175.

    Morgenthaler T, Kramer M, Alessi C et al.. Practice parameters for the psychological and behavioral treatment of insomnia: an update. An American Academy of Sleep Medicine report. Sleep 2006;29:14151419.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 176.

    Schutte-Rodin S, Broch L, Buysse D et al.. Clinical guideline for the evaluation and management of chronic insomnia in adults. J Clin Sleep Med 2008;4:487504.

  • 177.

    Hanna A, Sledge G, Mayer ML et al.. A phase II study of methylphenidate for the treatment of fatigue. Support Care Cancer 2006;14:210215.

  • 178.

    Lower EE, Fleishman S, Cooper A et al.. Efficacy of dexmethylphenidate for the treatment of fatigue after cancer chemotherapy: a randomized clinical trial. J Pain Symptom Manage 2009;38:650662.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 179.

    Morrow GR, Gillies LJ, Hickok JT et al.. The positive effect of the psychostimulant modafinil on fatigue from cancer that persists after treatment is completed [abstract]. J Clin Oncol 2005;23(Suppl):Abstract 8012.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 180.

    Kaleita T, Cloughesy J, Ford W. A pilot study of modafinil (Provigil®) for treatment of fatigue and neurobehavioral dysfunction in adult brain tumor patients [abstract]. Presented at the Ninth Annual Meeting of the Society for Neuro-Oncology; November 18–21, 2004; Toronto, Ontario, Canada. Abstract QL-06.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 181.

    Spathis A, Fife K, Blackhall F et al.. Modafinil for the treatment of fatigue in lung cancer: results of a placebo-controlled, double-blind, randomized trial. J Clin Oncol 2014;32:18821888.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 182.

    Yennurajalingam S, Bruera E. Palliative management of fatigue at the close of life: “it feels like my body is just worn out”. JAMA 2007;297:295304.

  • 183.

    Krishnasamy M. Fatigue in advanced cancer —meaning before measurement? Int J Nurs Stud 2000;37:401414.

  • 184.

    Lundh Hagelin C, Seiger A, Furst CJ. Quality of life in terminal care—with special reference to age, gender and marital status. Support Care Cancer 2006;14:320328.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 185.

    Walsh D, Donnelly S, Rybicki L. The symptoms of advanced cancer: relationship to age, gender, and performance status in 1,000 patients. Support Care Cancer 2000;8:175179.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 186.

    Walsh D, Rybicki L. Symptom clustering in advanced cancer. Support Care Cancer 2006;14:831836.

  • 187.

    Given B, Given C, Azzouz F, Stommel M. Physical functioning of elderly cancer patients prior to diagnosis and following initial treatment. Nurs Res 2001;50:222232.

  • 188.

    Wolfe J, Grier HE, Klar N et al.. Symptoms and suffering at the end of life in children with cancer. N Engl J Med 2000;342:326333.

  • 189.

    Wong RK, Franssen E, Szumacher E et al.. What do patients living with advanced cancer and their carers want to know? A needs assessment. Support Care Cancer 2002;10:408415.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 190.

    Mystakidou K, Parpa E, Katsouda E et al.. The role of physical and psychological symptoms in desire for death: a study of terminally ill cancer patients. Psychooncology 2006;15:355360.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 191.

    Miovic M, Block S. Psychiatric disorders in advanced cancer. Cancer 2007;110:16651676.

  • 192.

    Brady MJ, Peterman AH, Fitchett G et al.. A case for including spirituality in quality of life measurement in oncology. Psychooncology 1999;8:417428.

  • 193.

    Breitbart W, Rosenfeld B, Gibson C et al.. Meaning-centered group psychotherapy for patients with advanced cancer: a pilot randomized controlled trial. Psychooncology 2010;19:2128.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 194.

    Breitbart W, Poppito S, Rosenfeld B et al.. Pilot randomized controlled trial of individual meaning-centered psychotherapy for patients with advanced cancer. J Clin Oncol 2012;30:13041309.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 195.

    Chochinov HM, Kristjanson LJ, Breitbart W et al.. Effect of dignity therapy on distress and end-of-life experience in terminally ill patients: a randomised controlled trial. Lancet Oncol 2011;12:753762.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 196.

    Oldervoll LM, Loge JH, Paltiel H et al.. The effect of a physical exercise program in palliative care: a phase II study. J Pain Symptom Manage 2006;31:421430.

  • 197.

    Porock D, Kristjanson LJ, Tinnelly K et al.. An exercise intervention for advanced cancer patients experiencing fatigue: a pilot study. J Palliat Care 2000;16:3036.

  • 198.

    Strong A, Karavatas G, Reicherter EA. Recommended exercise protocol to decrease cancer-related fatigue and muscle wasting in patients with multiple myeloma: an evidence-based systematic review. Top Geriatr Rehabil 2006;22:172186.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 199.

    Sarhill N, Walsh D, Nelson KA et al.. Methylphenidate for fatigue in advanced cancer: a prospective open-label pilot study. Am J Hosp Palliat Care 2001;18:187192.

  • 200.

    Bruera E, Driver L, Barnes EA et al.. Patient-controlled methylphenidate for the management of fatigue in patients with advanced cancer: a preliminary report. J Clin Oncol 2003;21:44394443.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 201.

    Bruera E, Valero V, Driver L et al.. Patient-controlled methylphenidate for cancer fatigue: a double-blind, randomized, placebo-controlled trial. J Clin Oncol 2006;24:20732078.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 202.

    Bruera E, Yennurajalingam S, Palmer JL et al.. Methylphenidate and/or a nursing telephone intervention for fatigue in patients with advanced cancer: a randomized, placebo-controlled, phase II trial. J Clin Oncol 2013;31:24212427.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 203.

    Auret KA, Schug SA, Bremner AP, Bulsara M. A randomized, double-blind, placebo-controlled trial assessing the impact of dexamphetamine on fatigue in patients with advanced cancer. J Pain Symptom Manage 2009;37:613621.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 204.

    Hardy JR, Rees E, Ling J et al.. A prospective survey of the use of dexamethasone on a palliative care unit. Palliat Med 2001;15:38.

  • 205.

    Peuckmann V, Elsner F, Krumm N et al.. Pharmacological treatments for fatigue associated with palliative care. Cochrane Database Syst Rev 2010:CD006788.

  • 206.

    Matsuo N, Morita T, Iwase S. Physician-reported corticosteroid therapy practices in certified palliative care units in Japan: a nationwide survey. J Palliat Med 2012;15:10111016; quiz 1117–1018.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 207.

    Matsuo N, Morita T, Iwase S. Efficacy and undesirable effects of corticosteroid therapy experienced by palliative care specialists in Japan: a nationwide survey. J Palliat Med 2011;14:840845.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 208.

    Yennurajalingam S, Frisbee-Hume S, Palmer JL et al.. Reduction of cancer-related fatigue with dexamethasone: a double-blind, randomized, placebo-controlled trial in patients with advanced cancer. J Clin Oncol 2013;31:30763082.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 209.

    Paulsen O, Klepstad P, Rosland JH et al.. Efficacy of methylprednisolone on pain, fatigue, and appetite loss in patients with advanced cancer using opioids: a randomized, placebo-controlled, double-blind trial. J Clin Oncol 2014;32:32213228.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 210.

    Aaronson NK, Ahmedzai S, Bergman B et al.. The European Organization for Research and Treatment of Cancer QLQ-C30: a quality-of-life instrument for use in international clinical trials in oncology. J Natl Cancer Inst 1993;85:365376.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 211.

    Pascual Lopez A, Roque i Figuls M, Urrutia Cuchi G et al.. Systematic review of megestrol acetate in the treatment of anorexia-cachexia syndrome. J Pain Symptom Manage 2004;27:360369.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 212.

    Minton O, Richardson A, Sharpe M et al.. A systematic review and meta-analysis of the pharmacological treatment of cancer-related fatigue. J Natl Cancer Inst 2008;100:11551166.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 213.

    Gong S, Sheng P, Jin H et al.. Effect of methylphenidate in patients with cancer-related fatigue: a systematic review and meta-analysis. PLoS One 2014;9:e84391.

  • 214.

    Berger AM, Mitchell SA, Jacobsen PB, Pirl WF. Screening, evaluation, and management of cancer-related fatigue: Ready for implementation to practice? CA Cancer J Clin 2015;65:190211.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 215.

    Borneman T, Piper BF, Sun VC et al.. Implementing the Fatigue Guidelines at one NCCN member institution: process and outcomes. J Natl Compr Canc Netw 2007;5:10921101.

  • 216.

    Piper BF, Borneman T, Sun VC et al.. Cancer-related fatigue: role of oncology nurses in translating National Comprehensive Cancer Network assessment guidelines into practice. Clin J Oncol Nurs 2008;12:3747.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • Collapse
  • Expand
  • NCCN Clinical Practice Guidelines in Oncology: Cancer-Related Fatigue, Version 2.2015

    Version 2.2015, 01-22-15 ©2015 National Comprehensive Cancer Network, Inc. All rights reserved. The NCCN Guidelines® and this illustration may not be reproduced in any form without the express written permission of NCCN®.

  • NCCN Clinical Practice Guidelines in Oncology: Cancer-Related Fatigue, Version 2.2015

    Version 2.2015, 01-22-15 ©2015 National Comprehensive Cancer Network, Inc. All rights reserved. The NCCN Guidelines® and this illustration may not be reproduced in any form without the express written permission of NCCN®.

  • NCCN Clinical Practice Guidelines in Oncology: Cancer-Related Fatigue, Version 2.2015

    Version 2.2015, 01-22-15 ©2015 National Comprehensive Cancer Network, Inc. All rights reserved. The NCCN Guidelines® and this illustration may not be reproduced in any form without the express written permission of NCCN®.

  • 1.

    Ahlberg K, Ekman T, Gaston-Johansson F, Mock V. Assessment and management of cancer-related fatigue in adults. Lancet 2003;362:640650.

  • 2.

    Collins JJ, Devine TD, Dick GS et al.. The measurement of symptoms in young children with cancer: the validation of the Memorial Symptom Assessment Scale in children aged 7–12. J Pain Symptom Manage 2002;23:1016.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 3.

    Wagner LI, Cella D. Fatigue and cancer: causes, prevalence and treatment approaches. Br J Cancer 2004;91:822828.

  • 4.

    Henry DH, Viswanathan HN, Elkin EP et al.. Symptoms and treatment burden associated with cancer treatment: results from a cross-sectional national survey in the U.S. Support Care Cancer 2008;16:791801.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 5.

    Hofman M, Ryan JL, Figueroa-Moseley CD et al.. Cancer-related fatigue: the scale of the problem. Oncologist 2007;12(Suppl 1):410.

  • 6.

    Portenoy RK, Kornblith AB, Wong G et al.. Pain in ovarian cancer patients. Prevalence, characteristics, and associated symptoms. Cancer 1994;74:907915.

  • 7.

    Ventafridda V, De Conno F, Ripamonti C et al.. Quality-of-life assessment during a palliative care programme. Ann Oncol 1990;1:415420.

  • 8.

    Curtis EB, Krech R, Walsh TD.