Article
Co-occurrence of EGFR sensitising and resistance mutations at diagnosis in NSCLC.
Irish journal of medical science - 1 May 2019
Kelly Deirdre, Burke Louise, O'Brien Cathal, Kearns Rachel, Rafee Shareen, Power Derek, O'Reilly Seamus, O'Mahony Deirdre, Bambury Richard
Abstract excerpt
BACKGROUND: De novo epidermal growth factor receptor (EGFR) resistance mutations in tyrosine kinase inhibitor-naïve patients are rare when assessed by standard genotyping methods. METHODS: Patients with EGFR mutations were identified using PCR-based fragment length analysis, mass spectrometry-based genotyping (Sequenom), and Sanger sequencing. RESULTS: From 2008 to 2015, we observed de novo EGFR resistance...
Read the complete abstract on PubMedTopics
Share this publication in a Topic to start or enrich a Post.
