Artigo Acesso aberto Revisado por pares

Harnessing Clinical Sequencing Data for Survival Stratification of Patients With Metastatic Lung Adenocarcinomas

2019; Lippincott Williams & Wilkins; Issue: 3 Linguagem: Inglês

10.1200/po.18.00307

ISSN

2473-4284

Autores

Ronglai Shen, Axel Martin, Ai Ni, Matthew D. Hellmann, Kathryn C. Arbour, Emmet Jordan, Arshi Arora, Ryan Ptashkin, Ahmet Zehir, Mark G. Kris, Charles M. Rudin, Michael F. Berger, David B. Solit, Venkatraman Seshan, Maria E. Arcila, Marc Ladanyi, Gregory J. Riely,

Tópico(s)

Lung Cancer Research Studies

Resumo

Broad panel sequencing of tumors facilitates routine care of people with cancer as well as clinical trial matching for novel genome-directed therapies. We sought to extend the use of broad panel sequencing results to survival stratification and clinical outcome prediction.Using sequencing results from a cohort of 1,054 patients with advanced lung adenocarcinomas, we developed OncoCast, a machine learning tool for survival risk stratification and biomarker identification.With OncoCast, we stratified this patient cohort into four risk groups based on tumor genomic profile. Patients whose tumors harbored a high-risk profile had a median survival of 7.3 months (95% CI 5.5-10.9), compared to a low risk group with a median survival of 32.8 months (95% CI 26.3-38.5), with a hazard ratio of 4.6 (P<2e-16), far superior to any individual gene predictor or standard clinical characteristics. We found that co-mutations of both STK11 and KEAP1 are a strong determinant of unfavorable prognosis with currently available therapies. In patients with targetable oncogenes including EGFR/ALK/ROS1 and received targeted therapies, the tumor genetic background further differentiated survival with mutations in TP53 and ARID1A contributing to a higher risk score for shorter survival.Mutational profile derived from broad-panel sequencing presents an effective genomic stratification for patient survival in advanced lung adenocarcinoma. OncoCast is available as a public resource that facilitates the incorporation of mutational data to predict individual patient prognosis and compare risk characteristics of patient populations.

Referência(s)