Treatment options for immune-related adverse events associated with immune checkpoint inhibitors.

IF 6.8 2区 医学 Q1 PHARMACOLOGY & PHARMACY
Yu Hua Chen, Tamás Kovács, Péter Ferdinandy, Zoltán V Varga
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Abstract

The immunotherapy revolution with the use of immune checkpoint inhibitors (ICIs) started with the clinical use of the first ICI, ipilimumab, in 2011. Since then, the field of ICI therapy has rapidly expanded - with the FDA approval of 10 different ICI drugs so far and their incorporation into the therapeutic regimens of a range of malignancies. While ICIs have shown high anti-cancer efficacy, they also have characteristic side effects, termed immune-related adverse events (irAEs). These side effects hinder the therapeutic potential of ICIs and, therefore, finding ways to prevent and treat them is of paramount importance. The current protocols to manage irAEs follow an empirical route of steroid administration and, in more severe cases, ICI withdrawal. However, this approach is not optimal in many cases, as there are often steroid-refractory irAEs, and there is a potential for corticosteroid use to promote tumour progression. This review surveys the current alternative approaches to the treatments for irAEs, with the goal of summarizing and highlighting the best attempts to treat irAEs, without compromising anti-tumour immunity and allowing for rechallenge with ICIs after resolution of the irAEs.

Abstract Image

与免疫检查点抑制剂相关的免疫相关不良事件的治疗方案。
免疫检查点抑制剂(ICI)引发的免疫疗法革命始于2011年第一种ICI--伊匹单抗(ipilimumab)的临床应用。从那时起,ICI 治疗领域迅速扩大--迄今为止,美国食品及药物管理局已批准了 10 种不同的 ICI 药物,并将它们纳入了一系列恶性肿瘤的治疗方案。虽然 ICIs 具有很高的抗癌疗效,但它们也有一些特有的副作用,即免疫相关不良事件(irAEs)。这些副作用阻碍了 ICIs 的治疗潜力,因此,找到预防和治疗这些副作用的方法至关重要。目前处理 irAEs 的方案遵循经验性类固醇给药途径,在更严重的情况下,则会停用 ICI。然而,这种方法在很多情况下并不理想,因为通常会出现类固醇难治性虹膜睫状体异常,而且使用皮质类固醇有可能会促进肿瘤的进展。本综述调查了目前治疗虹膜睫状体异常的替代方法,目的是总结和强调治疗虹膜睫状体异常的最佳尝试,同时不损害抗肿瘤免疫力,并允许在虹膜睫状体异常缓解后重新使用 ICIs。
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来源期刊
CiteScore
15.40
自引率
12.30%
发文量
270
审稿时长
2.0 months
期刊介绍: The British Journal of Pharmacology (BJP) is a biomedical science journal offering comprehensive international coverage of experimental and translational pharmacology. It publishes original research, authoritative reviews, mini reviews, systematic reviews, meta-analyses, databases, letters to the Editor, and commentaries. Review articles, databases, systematic reviews, and meta-analyses are typically commissioned, but unsolicited contributions are also considered, either as standalone papers or part of themed issues. In addition to basic science research, BJP features translational pharmacology research, including proof-of-concept and early mechanistic studies in humans. While it generally does not publish first-in-man phase I studies or phase IIb, III, or IV studies, exceptions may be made under certain circumstances, particularly if results are combined with preclinical studies.
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