Prognostic Gene Expression Profiling in Cutaneous Melanoma: Identifying the Knowledge Gaps and Assessing the Clinical Benefit

Douglas Grossman, Nwanneka Okwundu, Edmund K. Bartlett, Michael A. Marchetti, Megan Othus, Daniel G. Coit, Rebecca I. Hartman, Sancy A. Leachman, Elizabeth G. Berry, Larissa Korde, Sandra J. Lee, Menashe Bar-Eli, Marianne Berwick, Tawnya Bowles, Elizabeth I. Buchbinder, Elizabeth M. Burton, Emily Y. Chu, Clara Curiel-Lewandrowski, Julia A. Curtis, Adil DaudDekker C. Deacon, Laura K. Ferris, Jeffrey E. Gershenwald, Kenneth F. Grossmann, Siwen Hu-Lieskovan, John Hyngstrom, Joanne M. Jeter, Robert L. Judson-Torres, Kari L. Kendra, Caroline C. Kim, John M. Kirkwood, David H. Lawson, Philip D. Leming, Georgina V. Long, Ashfaq A. Marghoob, Janice M. Mehnert, Michael E. Ming, Kelly C. Nelson, David Polsky, Richard A. Scolyer, Eric A. Smith, Vernon K. Sondak, Mitchell S. Stark, Jennifer A. Stein, John A. Thompson, John A. Thompson, Suraj S. Venna, Maria L. Wei, Susan M. Swetter

Research output: Contribution to journalReview article

7 Citations (Scopus)

Abstract

Importance: Use of prognostic gene expression profile (GEP) testing in cutaneous melanoma (CM) is rising despite a lack of endorsement as standard of care. Objective: To develop guidelines within the national Melanoma Prevention Working Group (MPWG) on integration of GEP testing into the management of patients with CM, including (1) review of published data using GEP tests, (2) definition of acceptable performance criteria, (3) current recommendations for use of GEP testing in clinical practice, and (4) considerations for future studies. Evidence Review: The MPWG members and other international melanoma specialists participated in 2 online surveys and then convened a summit meeting. Published data and meeting abstracts from 2015 to 2019 were reviewed. Findings: The MPWG members are optimistic about the future use of prognostic GEP testing to improve risk stratification and enhance clinical decision-making but acknowledge that current utility is limited by test performance in patients with stage I disease. Published studies of GEP testing have not evaluated results in the context of all relevant clinicopathologic factors or as predictors of regional nodal metastasis to replace sentinel lymph node biopsy (SLNB). The performance of GEP tests has generally been reported for small groups of patients representing particular tumor stages or in aggregate form, such that stage-specific performance cannot be ascertained, and without survival outcomes compared with data from the American Joint Committee on Cancer 8th edition melanoma staging system international database. There are significant challenges to performing clinical trials incorporating GEP testing with SLNB and adjuvant therapy. The MPWG members favor conducting retrospective studies that evaluate multiple GEP testing platforms on fully annotated archived samples before embarking on costly prospective studies and recommend avoiding routine use of GEP testing to direct patient management until prospective studies support their clinical utility. Conclusions and Relevance: More evidence is needed to support using GEP testing to inform recommendations regarding SLNB, intensity of follow-up or imaging surveillance, and postoperative adjuvant therapy. The MPWG recommends further research to assess the validity and clinical applicability of existing and emerging GEP tests. Decisions on performing GEP testing and patient management based on these results should only be made in the context of discussion of testing limitations with the patient or within a multidisciplinary group.

Original languageEnglish
Pages (from-to)1004-1011
Number of pages8
JournalJAMA Dermatology
Volume156
Issue number9
DOIs
Publication statusPublished - Sep 2020
Externally publishedYes

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