Phase Ib/II Study of Capmatinib (INC280) Plus Gefitinib After Failure of Epidermal Growth Factor Receptor (EGFR) Inhibitor Therapy in Patients With EGFR-Mutated, MET Factor–Dysregulated Non–Small-Cell Lung Cancer
Author(s) -
YiLong Wu,
Li Zhang,
DongWan Kim,
Xiaoqing Liu,
Dae Ho Lee,
James ChihHsin Yang,
MyungJu Ahn,
Johan Vansteenkiste,
WuChou Su,
Enriqueta Felip,
Vincent Chia,
Sabine Glaser,
Philippe Pultar,
Sylvia Zhao,
Bin Peng,
Mikhail Akimov,
Daniel S.W. Tan
Publication year - 2018
Publication title -
journal of clinical oncology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 10.482
H-Index - 548
eISSN - 1527-7755
pISSN - 0732-183X
DOI - 10.1200/jco.2018.77.7326
Subject(s) - gefitinib , medicine , rash , epidermal growth factor receptor , phases of clinical research , egfr inhibitors , clinical endpoint , peripheral edema , adverse effect , erlotinib , pharmacology , tyrosine kinase inhibitor , oncology , cancer , toxicity , clinical trial
MET dysregulation occurs in up to 26% of non-small-cell lung cancers (NSCLCs) after epidermal growth factor receptor (EGFR)-tyrosine kinase inhibitor (TKI) treatment. Capmatinib (INC280) is a potent and selective MET inhibitor with preclinical activity in combination with gefitinib in EGFR-mutant, MET-amplified/overexpressing models of acquired EGFR-TKI resistance. This phase Ib/II study investigated the safety and efficacy of capmatinib plus gefitinib in patients with EGFR-mutated, MET-dysregulated (amplified/overexpressing) NSCLC who experienced disease progression while receiving EGFR-TKI treatment.
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