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免疫检查点抑制剂相关毛细血管渗漏综合征:系统评价和全球药物警戒研究。

Immune checkpoint inhibitor-associated capillary leak syndrome: A systematic review and a worldwide pharmacovigilance study.

机构信息

CHR d'Orléans, Service de Médecine Interne, Orléans, France.

CHR d'Orléans, Service de Médecine-Intensive Réanimation, Orléans, France.

出版信息

J Intern Med. 2023 Jul;294(1):58-68. doi: 10.1111/joim.13641. Epub 2023 Apr 20.

DOI:10.1111/joim.13641
PMID:37038359
Abstract

BACKGROUND

Although a few case reports have shown that immune checkpoint inhibitors (ICIs) are potential inducers of capillary leak syndrome (CLS), an incidental finding cannot be ruled out. The aim of this study was to describe the clinical characteristics of ICI-induced CLS through a systematic review and to assess a potential safety signal.

METHODS

Medline/PubMed, Embase, and Reactions Weekly were screened, and a global disproportionality study was performed using the World Health Organization pharmacovigilance database through January 15, 2023. A signal of disproportionate reporting was defined as a Bayesian information component (IC) with a 95% credibility interval (CrI) lower boundary that exceeds 0.

RESULTS

A total of 47 cases of ICI-associated CLS were included, 14 from the systematic review (of 61 screened articles) and 33 from VigiBase (of 34,058,481 reports of adverse drug reactions). The median time to CLS onset from the start of ICI was 12 weeks (interquartile range 8-49, n = 24). A total of 57% (8/14) of patients experienced an immune-related adverse event (irAE) before CLS. A fatal outcome was reported in 23% (7/31) of patients. A significant overreporting of CLS was found with ICIs compared with all other drugs (IC 2.4, 95% CrI from 1.8 to 2.8).

CONCLUSION

This study showed a significant signal of disproportionality reporting for ICI-induced CLS, characterized by a long time to onset, and compared with the idiopathic form of the disease with a less abrupt onset and a less consistent hemoconcentration pattern.

摘要

背景

尽管少数病例报告表明免疫检查点抑制剂(ICI)可能是毛细血管渗漏综合征(CLS)的诱因,但不能排除偶发发现的可能性。本研究旨在通过系统评价描述 ICI 诱导的 CLS 的临床特征,并评估潜在的安全信号。

方法

筛选了 Medline/PubMed、Embase 和 Reactions Weekly,并通过 2023 年 1 月 15 日之前的世界卫生组织药物警戒数据库进行了全球不成比例研究。报告比例不成比例的信号定义为贝叶斯信息分量(IC)的 95%可信度区间(CrI)下限超过 0。

结果

共纳入 47 例与 ICI 相关的 CLS 病例,其中 14 例来自系统评价(61 篇筛选文章中),33 例来自 VigiBase(34058481 例药物不良反应报告中)。ICI 开始后 CLS 发病的中位时间为 12 周(四分位距 8-49,n=24)。57%(8/14)的患者在 CLS 发生前经历了免疫相关不良事件(irAE)。31%(7/31)的患者报告了致命结局。与所有其他药物相比,ICI 引起的 CLS 报告存在显著的不成比例(IC 2.4,95%CrI 为 1.8 至 2.8)。

结论

本研究显示 ICI 诱导的 CLS 报告存在显著的不成比例信号,其特征为发病时间较长,与疾病的特发性形式相比,发病更突然,血液浓缩模式不一致。

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