免疫相关不良事件后恢复免疫检查点抑制剂治疗。

IF 1.8 4区 医学 Q3 MEDICINE, RESEARCH & EXPERIMENTAL
In vivo Pub Date : 2025-07-01 DOI:10.21873/invivo.13983
Hirotaka Suto
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引用次数: 0

摘要

免疫相关不良事件(irAEs)是类似自身免疫性疾病的过度免疫反应,由免疫检查点抑制剂(ICIs)诱导,可影响全身器官。与常规细胞毒性抗癌药物相关的ae相反,ae可能在停止治疗后持续存在或复发。irAE复发的风险被认为取决于初始irAE的类型和严重程度,而反应率取决于再次给予ICIs的类型和顺序。因此,恢复ICI治疗的决定取决于先前irae的类型和严重程度,以及恢复治疗的预期获益和风险。这篇综述的重点是每次irAE后恢复ICI治疗的风险和益处,并总结了恢复ICI治疗的程序。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Resumption of Immune Checkpoint Inhibitor Therapy Following Immune-related Adverse Events.

Immune-related adverse events (irAEs) are excessive immune responses resembling autoimmune diseases, induced by immune checkpoint inhibitors (ICIs), and can affect organs throughout the body. In contrast to AEs associated with conventional cytotoxic anticancer agents, irAEs may persist or recur after treatment discontinuation. The risk of irAEs recurrence is thought to vary depending on the type and severity of the initial irAE, while the response rate depends on the type and sequence of ICIs re-administered. Therefore, the decision to resume ICI therapy depends on the type and severity of prior irAEs, as well as the anticipated benefits and risks of resumption. This review focuses on the risks and benefits of resuming ICI therapy after each irAE and summarizes the procedure for its resumption.

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来源期刊
In vivo
In vivo 医学-医学:研究与实验
CiteScore
4.20
自引率
4.30%
发文量
330
审稿时长
3-8 weeks
期刊介绍: IN VIVO is an international peer-reviewed journal designed to bring together original high quality works and reviews on experimental and clinical biomedical research within the frames of physiology, pathology and disease management. The topics of IN VIVO include: 1. Experimental development and application of new diagnostic and therapeutic procedures; 2. Pharmacological and toxicological evaluation of new drugs, drug combinations and drug delivery systems; 3. Clinical trials; 4. Development and characterization of models of biomedical research; 5. Cancer diagnosis and treatment; 6. Immunotherapy and vaccines; 7. Radiotherapy, Imaging; 8. Tissue engineering, Regenerative medicine; 9. Carcinogenesis.
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