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血液生化指标与抗生素暴露与接受 PD-1 抑制剂治疗的晚期癌症患者严重免疫相关不良事件的关联。

Association of Blood Biochemical Indexes and Antibiotic Exposure With Severe Immune-related Adverse Events in Patients With Advanced Cancers Receiving PD-1 Inhibitors.

机构信息

Departments of Radiation Oncology.

Medical Oncology, The Affiliated Cancer Hospital of Nanjing Medical University & Jiangsu Cancer Hospital & Jiangsu Institute of Cancer Research, Nanjing.

出版信息

J Immunother. 2022 May 1;45(4):210-216. doi: 10.1097/CJI.0000000000000415.

DOI:10.1097/CJI.0000000000000415
PMID:35250004
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8986630/
Abstract

Some patients with cancer treated with programmed death 1 (PD-1) inhibitors experience immune-related severe adverse events (ir-SAEs), however, predictors are limited. The objective was to identify clinicopathologic features that may be associated with a higher ir-SAE risk. This was a nested case-control study. After screening a total of 832 PD-1 inhibitor-treated patients, we identified 42 ir-SAE cases. According to the Common Terminology Criteria for Adverse Events (CTCAE) version 5.0, ir-SAEs were defined as grade ≥3 toxic effects associated with immunotherapy. A total of 126 controls were matched. The crude and adjusted risks of ir-SAEs were estimated by odds ratio (ORs) and 95% CIs using multivariate logistic regression models. Baseline neutrophil-to-lymphocyte ratio (NLR) [per SD increment-adjusted (aOR): 1.16], lactate dehydrogenase (LDH) ≥245 U/L (aOR: 2.39), and antibiotic exposure (aOR: 4.39) were associated with a higher risk of ir-SAEs. When NLR was categorized in 3 groups, significantly higher risks of ir-SAEs (aOR: 4.95) were found in participants in group 3 (>6) than in those in group 1 (<3). Furthermore, NLR (per SD increment-adjusted hazard ratio:1.08) were also significantly associated with shorter overall survival (OS). Baseline LDH ≥245 U/L and antibiotic exposure were no significant association with OS. In conclusion, ir-SAEs were associated between baseline NLR, LDH ≥245 U/L and antibiotic exposure. Lower NLR was correlated with longer OS for cancer.

摘要

一些接受程序性死亡 1 (PD-1) 抑制剂治疗的癌症患者经历免疫相关的严重不良事件 (ir-SAEs),但预测因素有限。本研究的目的是确定可能与更高的 ir-SAE 风险相关的临床病理特征。这是一项嵌套病例对照研究。在筛选了总共 832 名接受 PD-1 抑制剂治疗的患者后,我们确定了 42 例 ir-SAE 病例。根据不良事件通用术语标准 (CTCAE) 第五版,ir-SAEs 定义为与免疫治疗相关的≥3 级毒性作用。共匹配了 126 个对照。使用多变量逻辑回归模型,通过比值比 (OR) 和 95%置信区间 (CI) 估计 ir-SAEs 的粗风险和调整风险。基线中性粒细胞与淋巴细胞比值 (NLR) [每标准差增量调整 (aOR):1.16]、乳酸脱氢酶 (LDH) ≥245 U/L(aOR:2.39)和抗生素暴露 (aOR:4.39)与 ir-SAEs 的风险增加相关。当 NLR 分为 3 组时,与 NLR 处于第 1 组(<3)的患者相比,第 3 组(>6)的患者发生 ir-SAEs 的风险显著更高(aOR:4.95)。此外,NLR (每标准差增量调整的风险比:1.08)也与总生存期 (OS) 显著相关。基线 LDH ≥245 U/L 和抗生素暴露与 OS 无显著相关性。总之,基线 NLR、LDH ≥245 U/L 和抗生素暴露与 ir-SAEs 相关。较低的 NLR 与癌症患者的更长 OS 相关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef49/8986630/b8aa7e50653c/cji-45-210-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef49/8986630/f031555f6a9f/cji-45-210-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef49/8986630/11d697a2c42d/cji-45-210-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef49/8986630/b8aa7e50653c/cji-45-210-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef49/8986630/f031555f6a9f/cji-45-210-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef49/8986630/11d697a2c42d/cji-45-210-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef49/8986630/b8aa7e50653c/cji-45-210-g003.jpg

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