医学
T790米
肺癌
内科学
表皮生长因子受体
吉非替尼
突变
抗药性
表皮生长因子受体抑制剂
肿瘤科
抗性突变
癌症研究
癌症
酪氨酸激酶
酪氨酸激酶抑制剂
受体
生物
基因
遗传学
聚合酶链反应
逆转录酶
作者
Pasi A. Jänne,James Chih‐Hsin Yang,Dong‐Wan Kim,David Planchard,Yuichiro Ohe,Suresh S. Ramalingam,Myung‐Ju Ahn,Sang-We Kim,Wu‐Chou Su,Leora Horn,Daniel Haggstrom,Enriqueta Felip,Joo-Hang Kim,Paul Frewer,Mireille Cantarini,Kathryn H. Brown,Paul A. Dickinson,Serban Ghiorghiu,Malcolm Ranson
标识
DOI:10.1056/nejmoa1411817
摘要
The EGFR T790M mutation is the most common mechanism of drug resistance to epidermal growth factor receptor (EGFR) tyrosine kinase inhibitors in patients who have lung cancer with an EGFR mutation (EGFR-mutated lung cancer). In preclinical models, the EGFR inhibitor AZD9291 has been shown to be effective against both EGFR tyrosine kinase inhibitor–sensitizing and T790M resistance mutations.
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