Compliance With NCCN Guidelines for Evaluation and Treatment of Anemia Among Patients With Solid Tumors

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Demetra Hypatia Hufnagel Vanderbilt University School of Medicine, Nashville, TN
Department of Obstetrics and Gynecology, University of California, Los Angeles, Los Angeles, CA

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Lia Manfredi Bos Division of Gynecologic Oncology, Department of Obstetrics and Gynecology, University of Alabama, Birmingham, AL

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Alaina Johnson Brown Division of Gynecologic Oncology, Department of Obstetrics and Gynecology, Vanderbilt University Medical Center, Nashville, TN

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Lauren Shore Prescott Division of Gynecologic Oncology, Department of Obstetrics and Gynecology, Vanderbilt University Medical Center, Nashville, TN

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Background: NCCN Guidelines for Hematopoietic Growth Factors recommend evaluation and treatment of anemia in patients with cancer. However, a paucity of data exists regarding compliance with these recommendations. Methods: A retrospective cohort study was performed of patients diagnosed with any solid tumor at Vanderbilt University Medical Center from 2008 to 2017. Tumor registry–confirmed cancer cases were identified by ICD-O codes using the Synthetic Derivative database. Anemia was defined as hemoglobin (Hgb) level ≤11 g/dL and graded according to CTCAE version 5.0. Absolute, functional, and possible functional iron deficiency were defined based on NCCN Guidelines. Results: A total of 25,018 patients met inclusion criteria. Median age was 60 years. The most common malignancies were respiratory tract, prostate, and nonprostate urologic (11% each). Among 8,695 patients with Hgb levels available prior to diagnosis, 1,484 (17%) were noted to be anemic proximal to diagnosis. Of the 25,018 patients, 11,019 (44%) were anemic within 6 months of diagnosis. Of these patients, 4,686 (43%) had grade 2 (moderate) anemia and 9,623 (87%) had normocytic anemia. Patients with retroperitoneal/peritoneal cancers had the highest prevalence of anemia (83/110; 75%). A total of 4,125 (37%) underwent any evaluation of their anemia, of whom 1,742 (16%) had iron studies performed and 1,528 (14%) had vitamin B12 or folate studies performed. Fewer than half of patients with anemia received treatment (n=4,318; 39%), including blood transfusion (n=3,528; 32%), oral iron supplementation (n=1,279; 12%), or intravenous iron supplementation (n=97; 1%). Anemia treatment was significantly more frequent as the grade of anemia increased (any treatment among grade 1/mild: 12%; grade 2/moderate: 31%; grade 3/severe: 77%; χ2 [2, n=11,019]=3,020.6; P<.001). Patients with penile and testicular cancers had the highest prevalence of anemia evaluation (n=57; 79%). Conclusions: Anemia is common in patients with solid tumors; yet, compliance with NCCN Guidelines for evaluation and treatment of anemia remains low. There are opportunities to improve compliance with guidelines across the spectrum of cancer care.

Submitted March 6, 2023; final revision received October 16, 2023; accepted for publication November 8, 2023. Published online March 15, 2024.

Author contributions: Conceptualization: Brown, Prescott. Collection and assembly of data: Hufnagel, Prescott. Data analysis and interpretation: Hufnagel, Bos, Prescott. Manuscript writing: Hufnagel, Prescott. Manuscript editing and final approval: All authors.

Disclosures: The authors have disclosed that they have not received any financial consideration from any person or organization to support the preparation, analysis, results, or discussion of this article.

Funding: This project was supported by the Vanderbilt Institute for Clinical and Translational Research (VICTR) Voucher VR54036 (L.S. Prescott). VICTR is funded by the National Center for Advancing Translational Sciences Clinical Sciences of the National Institutes of Health under award number UL1TR000445.

Disclaimer: The content is solely the responsibility of the authors and does not necessarily represent the official views of the National Center for Advancing Translational Sciences or the National Institutes of Health.

Supplementary material: Supplementary material associated with this article is available online at doi:10.6004/jnccn.2023.7108. The supplementary material has been supplied by the author(s) and appears in its originally submitted form. It has not been edited or vetted by JNCCN. All contents and opinions are solely those of the author. Any comments or questions related to the supplementary materials should be directed to the corresponding author.

Correspondence: Lauren Shore Prescott, MD, MPH, Division of Gynecologic Oncology, Department of Obstetrics and Gynecology, Vanderbilt University Medical Center, 1301 Medical Center Drive, Nashville, TN 37203. Email: lauren.prescott@vumc.org

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