| Literature DB >> 28149768 |
Jaydira Del Rivero1, Lindsey Enewold2, Anish Thomas3.
Abstract
Epidermal growth factor receptor (EGFR) mutations are the most frequent targetable genetic abnormality observed in non-small cell lung cancer (NSCLC). More than a decade after EGFR mutations were shown to predict sensitivity to EGFR-tyrosine kinase inhibitors (EGFR-TKI), retrospective cohort studies are now identifying and characterizing 5-year survivors. While these studies indicate subsets of patients achieving long-term survival, there is paucity of data pertaining to the long-term survival benefits of these targeted therapies at a population level. Improving access to molecular testing and treatment are key to maximizing the survival benefits at a population level.Entities:
Keywords: Lung cancer; epidermal growth factor receptor (EGFR); erlotinib; genetics; survival
Year: 2016 PMID: 28149768 PMCID: PMC5233873 DOI: 10.21037/tlcr.2016.11.08
Source DB: PubMed Journal: Transl Lung Cancer Res ISSN: 2218-6751