| Literature DB >> 32552277 |
Andrew J Piper-Vallillo1,2,3, Lecia V Sequist2,3, Zofia Piotrowska2,3.
Abstract
Since its approval in April 2018, osimertinib has been widely adopted as first-line therapy for patients with advanced EGFR-mutant non -small cell lung cancer (NSCLC). Understanding osimertinib resistance mechanisms and currently available treatment options are essential to selecting optimal second line therapy for patients whose disease progresses during front-line osimertinib. Using data compiled from 6 osimertinib-resistance series, we describe here the heterogeneous profile of EGFR-dependent and independent mechanisms of osimertinib treatment failure. We identified MET alterations (7%-24%), EGFR C797X (0%-29%), SCLC transformation (2%-15%), and oncogene fusions (1%-10%) as the most common mechanisms of resistance. This review provides an evidence-based, algorithmic approach to the evaluation and management of post-osimertinib progression as well as a compendium of active, enrolling clinical trials for this population.Entities:
Year: 2020 PMID: 32552277 DOI: 10.1200/JCO.19.03123
Source DB: PubMed Journal: J Clin Oncol ISSN: 0732-183X Impact factor: 44.544