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检查点抑制剂诱导的免疫相关不良事件的生物标志物——综述

Biomarkers of Checkpoint Inhibitor Induced Immune-Related Adverse Events-A Comprehensive Review.

作者信息

Hommes Josefien W, Verheijden Rik J, Suijkerbuijk Karijn P M, Hamann Dörte

机构信息

Center for Translational Immunology, University Medical Center Utrecht, Utrecht, Netherlands.

Department of Medical Oncology, Cancer Center, University Medical Center Utrecht, Utrecht, Netherlands.

出版信息

Front Oncol. 2021 Feb 11;10:585311. doi: 10.3389/fonc.2020.585311. eCollection 2020.

Abstract

Immune checkpoint inhibitors (ICIs) have substantially improved the prognosis of patients with different types of cancer. Through blockade of cytotoxic T-lymphocyte antigen 4 (CTLA-4) and programmed cell death protein 1 (PD-1), negative feedback mechanisms of the immune system are inhibited, potentially resulting in very durable anti-tumor responses. Despite their promise, ICIs can also elicit auto-immune toxicities. These immune-related adverse events (irAEs) can be severe and sometimes even fatal. Therefore, being able to predict severe irAEs in patients would be of added value in clinical decision making. A search was performed using "adverse events", "immune checkpoint inhibitor", "biomarker", and synonyms in PubMed, yielding 3580 search results. After screening title and abstract on the relevance to the review question, statistical significance of reported potential biomarkers, and evaluation of the remaining full papers, 35 articles were included. Five additional reports were obtained by means of citations and by using the similar article function on PubMed. The current knowledge is presented in comprehensive tables summarizing blood-based, immunogenetic and microbial biomarkers predicting irAEs prior to and during ICI therapy. Until now, no single biomarker has proven to be sufficiently predictive for irAE development. Recommendations for further research on this topic are presented.

摘要

免疫检查点抑制剂(ICIs)显著改善了不同类型癌症患者的预后。通过阻断细胞毒性T淋巴细胞抗原4(CTLA-4)和程序性细胞死亡蛋白1(PD-1),免疫系统的负反馈机制受到抑制,从而有可能产生非常持久的抗肿瘤反应。尽管前景广阔,但ICIs也会引发自身免疫毒性。这些免疫相关不良事件(irAEs)可能很严重,有时甚至会致命。因此,能够预测患者的严重irAEs对临床决策具有额外价值。在PubMed中使用“不良事件”、“免疫检查点抑制剂”、“生物标志物”及其同义词进行检索,得到3580条检索结果。在筛选标题和摘要与综述问题的相关性、所报道潜在生物标志物的统计学意义,并评估其余全文后,纳入了35篇文章。通过引用以及使用PubMed上的相似文章功能又获得了5篇报告。目前的知识以综合表格的形式呈现,总结了在ICI治疗之前和期间预测irAEs的基于血液的、免疫遗传学和微生物生物标志物。到目前为止,尚未证实有单一生物标志物对irAE的发生具有足够的预测性。本文还提出了关于该主题进一步研究的建议。

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