医学
内科学
PD-L1
抗体
免疫抑制
胃肠病学
无容量
免疫系统
癌症
肿瘤科
免疫疗法
免疫学
作者
Takehiro Tozuka,Noriko Yanagitani,Hiroshi Yoshida,Ryo Manabe,Shinsuke Ogusu,Ryosuke Tsugitomi,Hiroaki Sakamoto,Yoshiaki Amino,Ryo Ariyasu,Ken Uchibori,Satoru Kitazono,Masahiro Seike,Akihiko Gemma,Makoto Nishio
出处
期刊:Anticancer Research
[Anticancer Research USA Inc.]
日期:2021-04-01
卷期号:41 (4): 2093-2100
被引量:12
标识
DOI:10.21873/anticanres.14980
摘要
Background/Aim: The Renin–Angiotensin system (RAS) induces immunosuppression in the tumor microenvironment, and RAS inhibitors (RASi) improve the tumor immune microenvironment. We evaluated the impact of RASi on the efficacy anti-programmed cell death-1/Ligand-1 (anti-PD-1/PD-L1) antibodies. Patients and Methods: This retrospective study analyzed non-small cell lung cancer (NSCLC) patients who received anti-PD-1/PD-L1 antibodies monotherapy as second- or later-line treatment. We classified patients into those with or without use of RASi. Results: A total of 256 NSCLC patients were included and 37 patients used RASi. The median PFS of patients treated with RASi was significantly longer than that of patients treated without (HR=0.59, 95%CI=0.40-0.88). The median OS of patients treated with RASi tended to be longer than that of patients treated without (HR=0.71, 95%CI=0.45-1.11). Conclusion: The use of RASi was associated with a significantly longer PFS in NSCLC patients treated with anti-PD-1/PD-L1 antibodies. RASi use may enhance the efficacy of anti-PD-1/PD-L1 antibodies.
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