Association of antibiotic treatment with immune-related adverse events in patients with cancer receiving immunotherapy

医学 内科学 肺癌 不利影响 癌症 回顾性队列研究 不良事件报告系统 抗生素 药物警戒 逻辑回归 肿瘤科 生物 微生物学
作者
Ying Jing,Xue Chen,Kunyan Li,Yaoming Liu,Zhao Zhang,Yiqing Chen,Yuan Liu,Yushu Wang,Steven H. Lin,Lixia Diao,Jing Wang,Yanyan Lou,Douglas B. Johnson,Xiang Chen,Hong Liu,Leng Han
出处
期刊:Journal for ImmunoTherapy of Cancer [BMJ]
卷期号:10 (1): e003779-e003779 被引量:64
标识
DOI:10.1136/jitc-2021-003779
摘要

To determine whether antibiotic treatment is a risk factor for immune-related adverse events (irAEs) across different patients with cancer receiving anti-PD-1/PD-L1 therapies.The retrospective analysis includes clinical information from 767 patients with cancer treated at Hunan Cancer Hospital from 2017 to 2020. The pharmacovigilance data analysis includes individual cases of 38,705 safety reports from the US Food and Drug Administration Adverse Event Reporting System (FAERS) from 2014 to 2020, and 25,122 cases of safety reports from the World Health Organization database VigiBase from 2014 to 2019. All cases that received anti-PD-1/PD-L1 treatment were included. Multiomics data from patients across 25 cancer types were download from The Cancer Genome Atlas. Logistic regression and propensity score algorithm was employed to calculate OR of irAEs.Retrospective analysis of in-house patients showed that irAE potential risks are higher in all cancer (OR 2.12, 95% CI 1.38 to 3.22, false discovery rate (FDR) adjusted-p=1.93×10-3) and patients with lung cancer (OR 3.16, 95% CI 1.67 to 5.95, FDR adjusted-p=1.93×10-3) when using antibiotics. Potential risk of irAEs in patients with lung cancer with antibiotic treatment is significantly higher in FAERS (OR 1.39, 95% CI 1.21 to 1.59; FDR adjusted-p=1.62×10-5) and VigiBase (OR 1.32, 95% CI 1.09 to 1.59, FDR adjusted-p=0.05). Mechanistically, decreased microbial diversity caused by antibiotics use may increase the irAE risk through mediating the irAE-related factors.Our study is the first to comprehensively demonstrate the associations of irAEs and antibiotic during anti-PD-1/PD-L1 therapy across a wide spectrum of cancers by analyzing multisource data. Administration of antibiotics should be carefully evaluated in patients with cancer treated by anti-PD-1/PD-L1 to avoid potentially increasing irAE risk.
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