免疫疗法
Notch信号通路
医学
癌症研究
肿瘤科
内科学
癌症
受体
作者
Zhimin Zhang,Yanyan Gu,Xiaona Su,Jing Bai,Wei Guan,Jungang Ma,Jia Luo,Juan He,Bicheng Zhang,Mingying Geng,Xuefeng Xia,Yanfang Guan,Cheng Shen,Chuan Chen
标识
DOI:10.3389/fonc.2021.659321
摘要
Although immune checkpoint inhibitors (ICIs) have shown remarkable benefit for treatment of advanced non-small lung cancer (NSCLC), only a minority of patients can achieve durable responses and the most patients produce an ultra-rapid progressive disease. Here, we collected the availably published datasets and mined the determinants of response to immunotherapy on pathway levels. One hundred six NSCLC patients treated with immunotherapy were combined from Rizvi et al. and Hellman et al. studies (whole exon sequencing). Two independent validation datasets consisted of the MSKCC cohort (targeted sequencing) and data by Anagnostou and colleagues (whole exon sequencing). The Cancer Genome Atlas (TCGA) somatic mutation and gene expression data were applied to explore the immunobiology features. In the first combined cohort, we detected NOTCH pathway altered in 71% patients with durable clinical benefit (DCB) while only 36% among no durable benefit (NDB) (p = 0.005). Compared to NDB group, co-occurrence of NOTCH and at least two DDR (co-DDR) pathway was discovered in DCB group and contributed to a prolonged progression-free survival (PFS) [22.1
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