TY - JOUR
T1 - 31-Gene Expression Profile Testing in Cutaneous Melanoma and Survival Outcomes in a Population-Based Analysis
T2 - A SEER Collaboration
AU - Bailey, Christine N.
AU - Martin, Brian J.
AU - Petkov, Valentina I.
AU - Schussler, Nicola C.
AU - Stevens, Jennifer L.
AU - Bentler, Suzanne
AU - Cress, Rosemary D.
AU - Doherty, Jennifer A.
AU - Durbin, Eric B.
AU - Gomez, Scarlett L.
AU - Gonsalves, Lou
AU - Hernandez, Brenda Y.
AU - Liu, Lihua
AU - Morawski, Bozena M.
AU - Schymura, Maria J.
AU - Schwartz, Stephen M.
AU - Ward, Kevin C.
AU - Wiggins, Charles
AU - Wu, Xiao Cheng
AU - Goldberg, Matthew S.
AU - Siegel, Jennifer J.
AU - Cook, Robert W.
AU - Covington, Kyle R.
AU - Kurley, Sarah J.
N1 - Publisher Copyright:
© 2023 American Society of Clinical Oncology.
PY - 2023
Y1 - 2023
N2 - PURPOSEThe DecisionDx-Melanoma 31-gene expression profile (31-GEP) test is validated to classify cutaneous malignant melanoma (CM) patient risk of recurrence, metastasis, or death as low (class 1A), intermediate (class 1B/2A), or high (class 2B). This study aimed to examine the effect of 31-GEP testing on survival outcomes and confirm the prognostic ability of the 31-GEP at the population level.METHODSPatients with stage I-III CM with a clinical 31-GEP result between 2016 and 2018 were linked to data from 17 SEER registries (n = 4,687) following registries' operation procedures for linkages. Melanoma-specific survival (MSS) and overall survival (OS) differences by 31-GEP risk category were examined using Kaplan-Meier analysis and the log-rank test. Crude and adjusted hazard ratios (HRs) were calculated using Cox regression model to evaluate variables associated with survival. 31-GEP tested patients were propensity score-matched to a cohort of non-31-GEP tested patients from the SEER database. Robustness of the effect of 31-GEP testing was assessed using resampling.RESULTSPatients with a 31-GEP class 1A result had higher 3-year MSS and OS than patients with a class 1B/2A or class 2B result (MSS: 99.7% v 97.1% v 89.6%, P <.001; OS: 96.6% v 90.2% v 79.4%, P <.001). A class 2B result was an independent predictor of MSS (HR, 7.00; 95% CI, 2.70 to 18.00) and OS (HR, 2.39; 95% CI, 1.54 to 3.70). 31-GEP testing was associated with a 29% lower MSS mortality (HR, 0.71; 95% CI, 0.53 to 0.94) and 17% lower overall mortality (HR, 0.83; 95% CI, 0.70 to 0.99) relative to untested patients.CONCLUSIONIn a population-based, clinically tested melanoma cohort, the 31-GEP stratified patients by their risk of dying from melanoma.
AB - PURPOSEThe DecisionDx-Melanoma 31-gene expression profile (31-GEP) test is validated to classify cutaneous malignant melanoma (CM) patient risk of recurrence, metastasis, or death as low (class 1A), intermediate (class 1B/2A), or high (class 2B). This study aimed to examine the effect of 31-GEP testing on survival outcomes and confirm the prognostic ability of the 31-GEP at the population level.METHODSPatients with stage I-III CM with a clinical 31-GEP result between 2016 and 2018 were linked to data from 17 SEER registries (n = 4,687) following registries' operation procedures for linkages. Melanoma-specific survival (MSS) and overall survival (OS) differences by 31-GEP risk category were examined using Kaplan-Meier analysis and the log-rank test. Crude and adjusted hazard ratios (HRs) were calculated using Cox regression model to evaluate variables associated with survival. 31-GEP tested patients were propensity score-matched to a cohort of non-31-GEP tested patients from the SEER database. Robustness of the effect of 31-GEP testing was assessed using resampling.RESULTSPatients with a 31-GEP class 1A result had higher 3-year MSS and OS than patients with a class 1B/2A or class 2B result (MSS: 99.7% v 97.1% v 89.6%, P <.001; OS: 96.6% v 90.2% v 79.4%, P <.001). A class 2B result was an independent predictor of MSS (HR, 7.00; 95% CI, 2.70 to 18.00) and OS (HR, 2.39; 95% CI, 1.54 to 3.70). 31-GEP testing was associated with a 29% lower MSS mortality (HR, 0.71; 95% CI, 0.53 to 0.94) and 17% lower overall mortality (HR, 0.83; 95% CI, 0.70 to 0.99) relative to untested patients.CONCLUSIONIn a population-based, clinically tested melanoma cohort, the 31-GEP stratified patients by their risk of dying from melanoma.
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U2 - 10.1200/PO.23.00044
DO - 10.1200/PO.23.00044
M3 - Article
C2 - 37384864
AN - SCOPUS:85179465195
VL - 7
JO - JCO Precision Oncology
JF - JCO Precision Oncology
M1 - e2300044
ER -