Tepotinib in Non–Small-Cell Lung Cancer with MET Exon 14 Skipping Mutations
Author(s) -
Paul K. Paik,
Enriqueta Felip,
R. Veillon,
Hiroshi Sakai,
Alexis B. Cortot,
Marina Chiara Garassino,
Julien Mazières,
Santiago Viteri,
Hélène Senellart,
Jan P. van Meerbeeck,
Jo Raskin,
Niels Reinmuth,
Pierfranco Conté,
Dariusz M. Kowalski,
Byoung Chul Cho,
Jyoti D. Patel,
Leora Horn,
Frank Griesinger,
JiYoun Han,
YoungChul Kim,
GeeChen Chang,
ChenLiang Tsai,
James ChihHsin Yang,
Yuh-Min Chen,
Egbert F. Smit,
Anthonie J. van der Wekken,
Terufumi Kato,
Dilafruz Juraeva,
Christopher Stroh,
Rolf Bruns,
Josef Straub,
Andreas Johne,
J. Scheele,
John V. Heymach,
Xiuning Le
Publication year - 2020
Publication title -
new england journal of medicine
Language(s) - English
Resource type - Journals
eISSN - 1533-4406
pISSN - 0028-4793
DOI - 10.1056/nejmoa2004407
Subject(s) - medicine , exon , lung cancer , biopsy , confidence interval , liquid biopsy , exon skipping , population , oncology , gastroenterology , cancer , gene , genetics , alternative splicing , biology , environmental health
A splice-site mutation that results in a loss of transcription of exon 14 in the oncogenic driver MET occurs in 3 to 4% of patients with non-small-cell lung cancer (NSCLC). We evaluated the efficacy and safety of tepotinib, a highly selective MET inhibitor, in this patient population.
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