阿替唑单抗
医学
肿瘤科
突变
肺癌
内科学
程序性细胞死亡1
表皮生长因子受体
癌症研究
PD-L1
免疫疗法
癌症
彭布罗利珠单抗
遗传学
基因
生物
作者
Ying Liu,Wei Zhang,Qian Chen,Hui Wang,Yue Wang,Hui Xia,Wei Chen,Ningjing Liu,Бо Лю,X. Wang
标识
DOI:10.1016/j.jtho.2023.09.542
摘要
Although immune checkpoint inhibitors (ICIs) targeting the programmed cell death 1 (PD-1)/programmed cell death ligand 1 (PD-L1) axis have improved the survival of patients with advanced non-small cell lung cancer (NSCLC), their efficacy in EGFR-mutated NSCLC is largely restricted in either first- or more advanced-line settings [1,2]. Previous studies have reported that co-mutations have profound impacts on the efficacy of ICIs [3]. Most EGFR-mutated NSCLC patients also have other mutations [4], but how these co-mutation patterns influence the effectiveness of ICIs is unclear.
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