Occult Primary, Version 3.2014

The NCCN Guidelines for Occult Primary tumors provide recommendations for the evaluation, workup, management, and follow-up of patients with occult primary tumors (cancers of unknown primary). These NCCN Guidelines Insights summarize major discussion points of the 2014 NCCN Occult Primary panel meeting. The panel discussed gene expression profiling (GEP) for the identification of the tissue of origin and concluded that, although GEP has a diagnostic benefit, a clinical benefit has not been demonstrated. The panel recommends against GEP as standard management, although 20% of the panel believes the diagnostic benefit of GEP warrants its routine use. In addition, the panel discussed testing for actionable mutations (eg, ALK) to help guide choice of therapy, but declined to add this recommendation.

Abstract

The NCCN Guidelines for Occult Primary tumors provide recommendations for the evaluation, workup, management, and follow-up of patients with occult primary tumors (cancers of unknown primary). These NCCN Guidelines Insights summarize major discussion points of the 2014 NCCN Occult Primary panel meeting. The panel discussed gene expression profiling (GEP) for the identification of the tissue of origin and concluded that, although GEP has a diagnostic benefit, a clinical benefit has not been demonstrated. The panel recommends against GEP as standard management, although 20% of the panel believes the diagnostic benefit of GEP warrants its routine use. In addition, the panel discussed testing for actionable mutations (eg, ALK) to help guide choice of therapy, but declined to add this recommendation.

NCCN: Continuing Education

Accreditation Statement

This activity has been designated to meet the educational needs of physicians, nurses, and pharmacists involved in the management of patients with cancer. There is no fee for this article. The National Comprehensive Cancer Network (NCCN) is accredited by the ACCME to provide continuing medical education for physicians. NCCN designates this journal-based CE activity for a maximum of 1.0 AMA PRA Category 1 Credit(s)™. Physicians should claim only the credit commensurate with the extent of their participation in the activity.

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This activity is accredited for 1.0 contact hour. Accreditation as a provider refers to recognition of educational activities only; accredited status does not imply endorsement by NCCN or ANCC of any commercial products discussed/displayed in conjunction with the educational activity. Kristina M. Gregory, RN, MSN, OCN, is our nurse planner for this educational activity.

National Comprehensive Cancer Network is accredited by the Accreditation Council for Pharmacy Education as a provider of continuing pharmacy education. NCCN designates this continuing education activity for 1.0 contact hour(s) (0.1 CEUs) of continuing education credit in states that recognize ACPE accredited providers. This is a knowledge-based activity. UAN: 0836-0000-14-007-H01-P

All clinicians completing this activity will be issued a certificate of participation. To participate in this journal CE activity: 1) review the learning objectives and author disclosures; 2) study the education content; 3) take the posttest with a 66% minimum passing score and complete the evaluation at http://education.nccn.org/node/48804; and 4) view/print certificate.

Release date: July 8, 2014; Expiration date: July 8, 2015

Learning Objectives:

Upon completion of this activity, participants will be able to:

  • Integrate into professional practice the updates to NCCN Guidelines for Occult Primary

  • Describe the rationale behind the decision-making process for developing the NCCN Guidelines for Occult Primary

F1NCCN Guidelines Insights: Occult Primary, Version 3.2014

Version 3.2014 © National Comprehensive Cancer Network, Inc. 2014, 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 12, 7; 10.6004/jnccn.2014.0093

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

Occult primary tumors, or cancers of unknown primary (CUPs), are defined as histologically proven metastatic malignant tumors whose primary site cannot be identified during pretreatment evaluation.1,2 These tumors have a wide variety of clinical presentations, and most patients have a poor prognosis. Patients with occult primary tumors often present with general complaints, such as anorexia and weight loss. Early dissemination, aggressiveness, and unpredictability of metastatic pattern are characteristic of these tumors.3 Life expectancy is very short, with a median survival of 6 to 9 months.4

Tissue of Origin Identification

In an attempt to identify the tissue of origin of occult primary tumors, biopsy specimens are often analyzed using immunohistochemistry (IHC).5-8 In addition, gene expression profiling (GEP, or gene signature profiling) or other molecular profiling assays have been developed to attempt to identify the tissue of origin in these patients.9,10 The hope is that through basing treatment on the suspected tumor type, patient outcomes will be improved.

Molecular Profiling

Talantov et al11 developed a GEP assay designed to detect tumors originating from the lung, breast, colon, ovary, pancreas, and prostate through evaluating the expression of 10 specific genes using real-time quantitative reverse-transcription polymerase chain reaction (qRT-PCR). In a blinded study, this assay identified the tissue of origin of metastatic carcinomas for which the primary was known in 204 of 260 tested samples, with an overall accuracy of 78%. Varadhachary et al12 assessed the feasibility of this assay retrospectively in 104 patients with CUPs. A presumed tissue of origin was identified in 61% of patients, and the results were believed to be compatible with clinicopathologic features and response to therapy in most cases.

Similarly, Ma et al13 developed a 92 gene-based qRT-PCR assay to identify the site of origin of metastatic tumors, especially in patients with CUPs. In a retrospective multicenter study, this assay identified primary sites in 75% of patients after the initial diagnosis of CUP.14 A more recent validation study of 149 archival tumor specimens found similar rates (74%-77%) of diagnostic accuracy compared with identified primary tumors, IHC diagnoses, and clinical/histologic findings.15 This test is commercially available.

Using a microarray approach, Monzon et al16,17 developed a 1550-gene test, which had an 88% sensitivity and a 99% specificity for diagnosing uncertain primary tumors in a blinded multicenter validation study.18 This test is also commercially available.

Another microarray GEP assay has been developed that assesses the expression of 495 genes to identify the tissue of origin.19 This assay has also been validated20 but is not currently commercially available in the United States. A recent feasibility study by GEFCAPI (Groupe d'Etude Français des Carcinomes de site Primitif Inconnu) found that use of this test changed clinical management in as many as 50% of cases.21 This group is planning a randomized phase III trial to assess changes in progression-free survival (PFS) between patients with CUP treated empirically and those treated based on results of GEP.

Another form of molecular profiling has recently generated some interest for its potential to identify the tissue of origin of CUPs. This assay is based on the presence of microRNAs (miRNAs), which are noncoding RNAs that regulate gene expression and show high tissue specificity.22-24 Using a panel of 48 miRNAs, blinded sets of samples were identified with an accuracy of 85% to 89%.22,23 When this assay was prospectively studied in patients with occult primary tumors, the tissue of origin diagnosed was consistent with clinical and/or pathologic features of the disease in 62 of 74 patients (84%).24 This assay is commercially available. This research group recently developed a second-generation microarray assessing the levels of 64 miRNAs to identify 42 tumor types.25 The assay was validated on a set of 509 blinded samples and showed a sensitivity of 85%.

Several GEP tests are now commercially available and are being evaluated in prospective clinical studies in an attempt to determine whether the information they provide translates into clinically meaningful benefit for patients.26 In one study, 32 patients whose tumors were classified as being of colorectal origin by 2 GEP assays (the 10-gene assay of Talantov et al11 and the 92-gene assay of Ma et al13) showed a response to colorectal chemotherapy regimens as expected for patients with stage IV colorectal cancer.27 Results from a prospective, nonrandomized phase II study of 289 patients with CUPs in which treatments were based on the identification of primary sites by the 92-gene assay showed that clinical features and response to treatment were generally consistent with assay results.26 Although the median survival time of 12.5 months in the subset of patients that received GEP-directed treatment was better than that in the predefined historical cohort, the panel believes that similar results might be expected from empiric use of these regimens in a group of patients with unknown primary cancer predominantly below the diaphragm who have good performance status (PS). Thus, the clinical benefit from use of these molecular assays, remains to be determined. A recent review compared 3 commercially available tests.28

IHC vs GEP

In a recent, blinded, multicenter study by Handorf et al,29 the diagnostic accuracy of the 1550-gene GEP assay was compared with that of IHC staining in a set of metastases from known primaries. The results indicated that the accuracies were similar, with 89% accuracy for GEP and 83% accuracy for IHC (P=.013). A similarly designed study by Weiss et al30 compared the 92-gene GEP assay with IHC and found similar results (79% accuracy for GEP vs 69% for IHC; P=.019). The Handorf study29 also showed that performing additional rounds of IHC testing after a first round generally failed to provide additional diagnostic information. The panel thus recommends that only one round of staining (8-10 stains) be performed when IHC is used.

Panel Recommendations Regarding Tissue of Origin Identification

Overall, the panel believes that neither IHC, a diagnostic tool in widespread use, nor GEP should be used indiscriminately. The panel finds it noteworthy that thus far the literature on GEP and IHC in the workup of CUPs has focused far more on establishing a tissue of origin than on establishing whether such identification leads to better outcomes in patients.

Currently, the panel believes that available outcomes data are not sufficient to recommend the routine use of molecular profiling in the workup of occult primary tumors; use of these tests is thus a category 3 recommendation. Therefore, although the panel recognizes the diagnostic benefit of GEP, most members have concerns that a clinical benefit has not been shown. However, some panelists believe the diagnostic benefit of GEP warrants its routine use. Consequently, the panel added a footnote to the 2014 version of the NCCN Guidelines explaining that the use of molecular profiling as standard management is a category 3 recommendation. Overall, the panel does not recommend molecular profiling for identifying tissue of origin as standard management in the diagnostic workup of patients with CUP.

Testing for Actionable Mutations

The panel also discussed whether to recommend testing for actionable mutations (eg, EGFR and ALK mutations if lung cancer is suspected), using either individual gene testing or comprehensive profiling, to guide choice of therapy. Identification of certain mutations would allow molecularly targeted agents to be given to patients in attempt to improve outcomes. For example, crizotinib is used in patients with locally advanced or metastatic non-small cell lung cancer positive for the ALK gene rearrangement,31-33 and could therefore be tried in patients with ALK mutations and CUPs of possible lung origin. The panel noted, however, that data in the CUP setting for such an approach are lacking. Furthermore, some panel members reported that they have not seen good results from such an approach in their clinical experience. For these reasons, the panel declined to add a recommendation for actionable mutation testing in the 2014 version of the guidelines.

Conclusions

These NCCN Guidelines Insights for Occult Primary tumors highlight the shift in consensus for the recommendation against routine molecular profiling for identifying tissue origin. This year, more panelists support GEP for standard diagnostic workup, because they believe the diagnostic benefit is sufficient to warrant this recommendation. However, most of the panelists still believe that a clinical benefit must be shown before GEP can be recommended as part of standard management (thus a statement was added explaining that the use of GEP is a category 3 recommendation). The panel also believes that, until more robust outcomes and comparative effectiveness data are available, pathologists and oncologists must collaborate on the judicious use of both GEP and IHC on a case-by-case basis, with the best possible individualized patient outcomes in mind.

The panel also discussed testing for actionable mutations, with the intention of administering molecularly targeted therapy, but did not include that recommendation, citing a lack of data showing a clinical benefit with this approach.

References

  • 1.

    GrecoFAHainsworthJD. Cancer of unknown primary site. In: DeVitaVTLawrenceTSRosenburgSA eds. DeBita Hellman and Rosenberg's Cancer: Principles & Practice of Oncology. Vol. 2. 8th ed.Philadelphia, PA: Lippincott Williams & Wilkins; 2008:23632387.

    • Search Google Scholar
    • Export Citation
  • 2.

    GrecoFAHainsworthJD. Tumors of unknown origin. CA Cancer J Clin1992;42:969115.

  • 3.

    PavlidisN. Cancer of unknown primary: biological and clinical characteristics. Ann Oncol2003;14(Suppl 3):iii1118.

  • 4.

    PavlidisNBriasoulisEHainsworthJGrecoFA. Diagnostic and therapeutic management of cancer of an unknown primary. Eur J Cancer2003;39:19902005.

    • Search Google Scholar
    • Export Citation
  • 5.

    DabbsDJ. Diagnostic Immunohistochemistry. 3rd ed.Philadelphia, PA: Saunders Elsevier; 2010.

  • 6.

    OienKA. Pathologic evaluation of unknown primary cancer. Semin Oncol2009;36:837.

  • 7.

    VaradhacharyGRGrecoFA. Overview of patient management and future directions in unknown primary carcinoma. Semin Oncol2009;36:7580.

  • 8.

    WickMR. Immunohistochemical approaches to the diagnosis of undifferentiated malignant tumors. Ann Diagn Pathol2008;12:7284.

  • 9.

    BenderRAErlanderMG. Molecular classification of unknown primary cancer. Semin Oncol2009;36:3843.

  • 10.

    MonzonFAKoenTJ. Diagnosis of metastatic neoplasms: molecular approaches for identification of tissue of origin. Arch Pathol Lab Med2010;134:216224.

    • Search Google Scholar
    • Export Citation
  • 11.

    TalantovDBadenJJatkoeT. A quantitative reverse transcriptase-polymerase chain reaction assay to identify metastatic carcinoma tissue of origin. J Mol Diagn2006;8:320329.

    • Search Google Scholar
    • Export Citation
  • 12.

    VaradhacharyGRTalantovDRaberMN. Molecular profiling of carcinoma of unknown primary and correlation with clinical evaluation. J Clin Oncol2008;26:44424448.

    • Search Google Scholar
    • Export Citation
  • 13.

    MaXJPatelRWangX. Molecular classification of human cancers using a 92-gene real-time quantitative polymerase chain reaction assay. Arch Pathol Lab Med2006;130:465473.

    • Search Google Scholar
    • Export Citation
  • 14.

    GrecoFASpigelDRYardleyDA. Molecular profiling in unknown primary cancer: accuracy of tissue of origin prediction. Oncologist2010;15:500506.

    • Search Google Scholar
    • Export Citation
  • 15.

    GrecoFALenningtonWJSpigelDRHainsworthJD. Molecular profiling diagnosis in unknown primary cancer: accuracy and ability to complement standard pathology. J Natl Cancer Inst2013;105:782790.

    • Search Google Scholar
    • Export Citation
  • 16.

    DumurCILyons-WeilerMSciulliC. Interlaboratory performance of a microarray-based gene expression test to determine tissue of origin in poorly differentiated and undifferentiated cancers. J Mol Diagn2008;10:6777.

    • Search Google Scholar
    • Export Citation
  • 17.

    MonzonFALyons-WeilerMButurovicLJ. Multicenter validation of a 1,550-gene expression profile for identification of tumor tissue of origin. J Clin Oncol2009;27:25032508.

    • Search Google Scholar
    • Export Citation
  • 18.

    MonzonFADumurCI. Diagnosis of uncertain primary tumors with the pathwork tissue-of-origin test. Expert Rev Mol Diagn2010;10:1725.

  • 19.

    HorlingsHMvan LaarRKKerstJM. Gene expression profiling to identify the histogenetic origin of metastatic adenocarcinomas of unknown primary. J Clin Oncol2008;26:44354441.

    • Search Google Scholar
    • Export Citation
  • 20.

    van LaarRKMaXJde JongD. Implementation of a novel microarray-based diagnostic test for cancer of unknown primary. Int J Cancer2009;125:13901397.

    • Search Google Scholar
    • Export Citation
  • 21.

    Gross-GoupilMMassardCLesimpleT. Identifying the primary site using gene expression profiling in patients with carcinoma of an unknown primary (CUP): a feasibility study from the GEFCAPI. Onkologie2012;35:5455.

    • Search Google Scholar
    • Export Citation
  • 22.

    RosenfeldNAharonovRMeiriE. MicroRNAs accurately identify cancer tissue origin. Nat Biotechnol2008;26:462469.

  • 23.

    RosenwaldSGiladSBenjaminS. Validation of a microRNA-based qRT-PCR test for accurate identification of tumor tissue origin. Mod Pathol2010;23:814823.

    • Search Google Scholar
    • Export Citation
  • 24.

    VaradhacharyGRSpectorYAbbruzzeseJL. Prospective gene signature study using microRNA to identify the tissue of origin in patients with carcinoma of unknown primary (CUP). Clin Cancer Res2011;17:40634070.

    • Search Google Scholar
    • Export Citation
  • 25.

    MeiriEMuellerWCRosenwaldS. A second-generation microRNA-based assay for diagnosing tumor tissue origin. Oncologist2012;17:801812.

  • 26.

    HainsworthJDRubinMSSpigelDR. Molecular gene expression profiling to predict the tissue of origin and direct site-specific therapy in patients with carcinoma of unknown primary site: a prospective trial of the Sarah Cannon research institute. J Clin Oncol2013;31:217223.

    • Search Google Scholar
    • Export Citation
  • 27.

    GrecoFALenningtonWJSpigelDR. Carcinoma of unknown primary site (CUP): outcomes in patients with a colorectal molecular profile treated with site-specific chemotherapy [abstract]. J Clin Oncol2011;29(Suppl):Abstract 3563.

    • Search Google Scholar
    • Export Citation
  • 28.

    HandorfCR. Gene expression analysis and immunohistochemistry in evaluation of cancer of unknown primary: time for a patient-centered approach. J Natl Compr Canc Netw2011;9:14151420.

    • Search Google Scholar
    • Export Citation
  • 29.

    HandorfCRKulkarniAGrenertJP. A multicenter study directly comparing the diagnostic accuracy of gene expression profiling and immunohistochemistry for primary site identification in metastatic tumors. Am J Surg Pathol2013;37:10671075.

    • Search Google Scholar
    • Export Citation
  • 30.

    WeissLMChuPSchroederBE. Blinded comparator study of immunohistochemical analysis versus a 92-gene cancer classifier in the diagnosis of the primary site in metastatic tumors. J Mol Diagn2013;15:263269.

    • Search Google Scholar
    • Export Citation
  • 31.

    CamidgeDRBangYKwakEL. Progression-free survival (PFS) from a phase I study of crizotinib (PF-02341066) in patients with ALK-positive non-small cell lung cancer (NSCLC) [abstract]. J Clin Oncol2011;29(Suppl 15):Abstract 2501.

    • Search Google Scholar
    • Export Citation
  • 32.

    CrinoLKimDRielyGJ. Initial phase II results with crizotinib in advanced ALK-positive non-small cell lung cancer (NSCLC): PROFILE 1005 [abstract]. J Clin Oncol2011;29(Suppl 15):Abstract 7514.

    • Search Google Scholar
    • Export Citation
  • 33.

    ShawATKimDWNakagawaK. Crizotinib versus chemotherapy in advanced ALK-positive lung cancer. N Engl J Med2013;368:23852394.

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    NCCN Guidelines Insights: Occult Primary, Version 3.2014

    Version 3.2014 © National Comprehensive Cancer Network, Inc. 2014, All rights reserved. The NCCN Guidelines® and this illustration may not be reproduced in any form without the express written permission of NCCN®.

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