医学
融合基因
内科学
肿瘤科
酪氨酸激酶
癌症
蛋白激酶结构域
酪氨酸激酶抑制剂
肺癌
受体酪氨酸激酶
癌症研究
基因
受体
遗传学
生物
突变体
作者
Justin F. Gainor,Giuseppe Curigliano,Robert C. Doebele,Jessica J. Lin,S.-H.I. Ou,Steven P. Miller,Christopher D. Turner,Vivek Subbiah
标识
DOI:10.1016/j.jtho.2020.10.027
摘要
Chromosomal rearrangements involving the RET receptor tyrosine kinase are validated oncogenic drivers in 1–2% of patients with NSCLC. Pralsetinib is a selective RET tyrosine kinase inhibitor that has demonstrated clinical activity in patients with NSCLC harboring a RET fusion. Here, we report potential mechanisms of resistance in patients with NSCLC whose disease progressed on pralsetinib.
科研通智能强力驱动
Strongly Powered by AbleSci AI