| Literature DB >> 34918545 |
Egbert F Smit1, Christophe Dooms2, Jo Raskin3, Ernest Nadal4, Lye M Tho5, Xiuning Le6, Julien Mazieres7, How S Hin8, Masahire Morise9, Viola W Zhu10, Daniel Tan11, Kristina H Holmberg12, Barbara Ellers-Lenz13, Svenja Adrian14, Sabine Brutlach15, Karl M Schumacher14, Niki Karachaliou14, Yi-Long Wu16.
Abstract
MET amplification (METamp), a mechanism of acquired resistance to EGFR tyrosine kinase inhibitors, occurs in up to 30% of patients with non-small-cell lung cancer (NSCLC) progressing on first-line osimertinib. Combining osimertinib with a MET inhibitor, such as tepotinib, an oral, highly selective, potent MET tyrosine kinase inhibitor, may overcome METamp-driven resistance. INSIGHT 2 (NCT03940703), an international, open-label, multicenter phase II trial, assesses tepotinib plus osimertinib in patients with advanced/metastatic EGFR-mutant NSCLC and acquired resistance to first-line osimertinib and METamp, determined centrally by fluorescence in situ hybridization (gene copy number ≥5 and/or MET/CEP7 ≥2) at time of progression. Patients will receive tepotinib 500 mg (450 mg active moiety) plus osimertinib 80 mg once-a-day. The primary end point is objective response, and secondary end points include duration of response, progression-free survival, overall survival and safety. Trial registration number: NCT03940703 (clinicaltrials.gov).Entities:
Keywords: EGFR tyrosine kinase inhibitors; MET amplification; non-small-cell lung cancer; osimertinib; tepotinib
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Year: 2021 PMID: 34918545 DOI: 10.2217/fon-2021-1406
Source DB: PubMed Journal: Future Oncol ISSN: 1479-6694 Impact factor: 3.404