| Literature DB >> 28838405 |
A Oztan1, S Fischer2, A B Schrock3, R L Erlich3, C M Lovly4, P J Stephens3, J S Ross3, V Miller3, S M Ali3, S-H I Ou5, L E Raez6.
Abstract
Mutations in the epidermal growth factor receptor (EGFR) are drivers for a subset of lung cancers. Osimertinib is a third-generation tyrosine kinase inhibitor (TKI) recently approved for the treatment of T790M-positive non-small cell lung cancer (NSCLC); however, acquired resistance to osimertinib is evident and resistance mechanisms remain incompletely defined. The EGFR G724S mutation was detected using hybrid-capture based comprehensive genomic profiling (CGP) and a hybrid-capture based circulating tumor DNA (ctDNA) assays in two cases of EGFR-driven lung adenocarcinoma in patients who had progressed on osimertinib treatment. This study demonstrates the importance of both tissue and blood based hybrid-capture based genomic profiling at disease progression to identifying novel resistance mechanisms in the clinic.Entities:
Keywords: Acquired resistance; EGFR; G724S; Lung cancer; Osimertinib; T790M
Mesh:
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Year: 2017 PMID: 28838405 DOI: 10.1016/j.lungcan.2017.07.002
Source DB: PubMed Journal: Lung Cancer ISSN: 0169-5002 Impact factor: 5.705