奥西默替尼
医学
内科学
突变体
肿瘤科
癌症研究
表皮生长因子受体
受体
埃罗替尼
基因
遗传学
生物
作者
Y. Yu,Nan Yang,Y. Zhang,H. Zhang,M. Li,Qingqing Yu,Jinhui Zhou,Xiuya Hu,Jike Fang,H. Zhao,J. Feng,Liang Li,Yichang Shu,Xiaohong Wang,Mengdan Sun,J. Zhang,M. Li,Yuan-Yuan Ren,Songlin Lu
标识
DOI:10.1016/j.annonc.2022.10.334
摘要
MET Amplification (METamp) commonly mediates resistance to EGFR TKIs in NSCLC patients with EGFR-mutation. Several clinical trials showed that the combination of MET inhibition with EGFR TKI is a promising therapeutic strategy to overcome the MET amplification-mediated resistance. SCC244 is a highly selective small molecular inhibitor of MET kinase. It was well tolerated and has shown favorable anti-tumor activities in patients with MET aberration as monotherapy in clinical studies.
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