医学
肺癌
靶向治疗
肝细胞生长因子受体
受体酪氨酸激酶
癌症研究
酪氨酸激酶抑制剂
酪氨酸激酶
外显子
肿瘤科
肝细胞生长因子
临床试验
C-Met公司
表皮生长因子受体
内科学
癌症
受体
基因
生物
遗传学
作者
Alexander Drilon,Federico Cappuzzo,Sai‐Hong Ignatius Ou,D. Ross Camidge
标识
DOI:10.1016/j.jtho.2016.10.014
摘要
Abstract
The hepatocyte growth factor receptor (MET) is a potential therapeutic target in a number of cancers, including NSCLC. In NSCLC, MET pathway activation is thought to occur through a diverse set of mechanisms that influence properties affecting cancer cell survival, growth, and invasiveness. Preclinical and clinical evidence suggests a role for MET activation as both a primary oncogenic driver in subsets of lung cancer and as a secondary driver of acquired resistance to targeted therapy in other genomic subsets. In this review, we explore the biology and clinical significance behind MET proto-oncogene receptor tyrosine kinase (MET) exon 14 alterations and MET amplification in NSCLC, the role of MET amplification in the setting of acquired resistance to EGFR tyrosine kinase inhibitor therapy in EGFR-mutant NSCLC, and the history of MET pathway inhibitor drug development in NSCLC, highlighting current strategies that enrich for biomarkers likely to be predictive of response. Whereas previous trials that focused on MET pathway–directed targeted therapy in unselected or MET-overexpressing NSCLC yielded largely negative results, more recent investigations focusing on MET exon 14 alterations and MET amplification have been notable for meaningful clinical responses to MET inhibitor therapy in a substantial proportion of patients.
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