Mutation Detection in Patients With Advanced Cancer by Universal Sequencing of Cancer-Related Genes in Tumor and Normal DNA vs Guideline-Based Germline Testing

Diana Mandelker(Memorial Sloan Kettering Cancer Center), Liying Zhang(Memorial Sloan Kettering Cancer Center), Yelena Kemel(Memorial Sloan Kettering Cancer Center), Zsofia K. Stadler(Memorial Sloan Kettering Cancer Center), Joseph Vijai(Kettering University), Ahmet Zehir(Memorial Sloan Kettering Cancer Center), Nisha Pradhan(Memorial Sloan Kettering Cancer Center), Angela G. Arnold(Memorial Sloan Kettering Cancer Center), Michael F. Walsh(Cornell University), Yirong Li(Memorial Sloan Kettering Cancer Center), Anoop R. Balakrishnan(Memorial Sloan Kettering Cancer Center), Aijazuddin Syed(Memorial Sloan Kettering Cancer Center), Meera Prasad(Memorial Sloan Kettering Cancer Center), Khédoudja Nafa(Memorial Sloan Kettering Cancer Center), Maria I. Carlo(Memorial Sloan Kettering Cancer Center), Karen A. Cadoo(Cornell University), Meg Sheehan(Memorial Sloan Kettering Cancer Center), Megan Harlan Fleischut(Memorial Sloan Kettering Cancer Center), Erin Salo‐Mullen(Memorial Sloan Kettering Cancer Center), Magan Trottier(Memorial Sloan Kettering Cancer Center), Steven M. Lipkin(Cornell University), Anne Lincoln(Memorial Sloan Kettering Cancer Center), Semanti Mukherjee(Kettering University), Vignesh Ravichandran(Memorial Sloan Kettering Cancer Center), Roy Cambria(Memorial Sloan Kettering Cancer Center), Jesse Galle(Memorial Sloan Kettering Cancer Center), Wassim Abida(Cornell University), Marcia E. Arcila(Memorial Sloan Kettering Cancer Center), Ryma Benayed(Memorial Sloan Kettering Cancer Center), Ronak Shah(Memorial Sloan Kettering Cancer Center), Kenneth H. Yu(Cornell University), Dean F. Bajorin(Cornell University), Jonathan Coleman(Memorial Sloan Kettering Cancer Center), Steven D. Leach(Memorial Sloan Kettering Cancer Center), Maeve A. Lowery(Cornell University), Julio García‐Aguilar(Memorial Sloan Kettering Cancer Center), Philip W. Kantoff(Memorial Sloan Kettering Cancer Center), Charles L. Sawyers(Memorial Sloan Kettering Cancer Center), Maura N. Dickler(Cornell University), Leonard B. Saltz(Memorial Sloan Kettering Cancer Center), Robert J. Motzer(Memorial Sloan Kettering Cancer Center), Eileen M. O’Reilly(Memorial Sloan Kettering Cancer Center), Howard I. Scher(Memorial Sloan Kettering Cancer Center), José Baselga(Memorial Sloan Kettering Cancer Center), David S. Klimstra(Memorial Sloan Kettering Cancer Center), David B. Solit(Kettering University), David M. Hyman(Memorial Sloan Kettering Cancer Center), Michael F. Berger(Memorial Sloan Kettering Cancer Center), Marc Ladanyi(Memorial Sloan Kettering Cancer Center), Mark E. Robson(Memorial Sloan Kettering Cancer Center), Kenneth Offit(Cornell University)
JAMA
September 5, 2017
Cited by 517

Abstract

Importance: Guidelines for cancer genetic testing based on family history may miss clinically actionable genetic changes with established implications for cancer screening or prevention. Objective: To determine the proportion and potential clinical implications of inherited variants detected using simultaneous sequencing of the tumor and normal tissue ("tumor-normal sequencing") compared with genetic test results based on current guidelines. Design, Setting, and Participants: From January 2014 until May 2016 at Memorial Sloan Kettering Cancer Center, 10 336 patients consented to tumor DNA sequencing. Since May 2015, 1040 of these patients with advanced cancer were referred by their oncologists for germline analysis of 76 cancer predisposition genes. Patients with clinically actionable inherited mutations whose genetic test results would not have been predicted by published decision rules were identified. Follow-up for potential clinical implications of mutation detection was through May 2017. Exposure: Tumor and germline sequencing compared with the predicted yield of targeted germline sequencing based on clinical guidelines. Main Outcomes and Measures: Proportion of clinically actionable germline mutations detected by universal tumor-normal sequencing that would not have been detected by guideline-directed testing. Results: Of 1040 patients, the median age was 58 years (interquartile range, 50.5-66 years), 65.3% were male, and 81.3% had stage IV disease at the time of genomic analysis, with prostate, renal, pancreatic, breast, and colon cancer as the most common diagnoses. Of the 1040 patients, 182 (17.5%; 95% CI, 15.3%-19.9%) had clinically actionable mutations conferring cancer susceptibility, including 149 with moderate- to high-penetrance mutations; 101 patients tested (9.7%; 95% CI, 8.1%-11.7%) would not have had these mutations detected using clinical guidelines, including 65 with moderate- to high-penetrance mutations. Frequency of inherited mutations was related to case mix, stage, and founder mutations. Germline findings led to discussion or initiation of change to targeted therapy in 38 patients tested (3.7%) and predictive testing in the families of 13 individuals (1.3%), including 6 for whom genetic evaluation would not have been initiated by guideline-based testing. Conclusions and Relevance: In this referral population with selected advanced cancers, universal sequencing of a broad panel of cancer-related genes in paired germline and tumor DNA samples was associated with increased detection of individuals with potentially clinically significant heritable mutations over the predicted yield of targeted germline testing based on current clinical guidelines. Knowledge of these additional mutations can help guide therapeutic and preventive interventions, but whether all of these interventions would improve outcomes for patients with cancer or their family members requires further study. Trial Registration: clinicaltrials.gov Identifier: NCT01775072.


Related Papers

No related papers found

Powered by citation graph analysis