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免疫疗法毒性:识别与管理。

Immunotherapy toxicity: identification and management.

机构信息

University of California Helen Diller Family Comprehensive Cancer Center, San Francisco, CA, USA.

出版信息

Breast Cancer Res Treat. 2022 Feb;192(1):1-17. doi: 10.1007/s10549-021-06480-5. Epub 2022 Jan 11.

DOI:10.1007/s10549-021-06480-5
PMID:35015209
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8841316/
Abstract

The widespread adoption of immunotherapy has revolutionized the treatment of various cancer types, including metastatic triple-negative breast cancer (TNBC), which has long been associated with poor prognostic outcomes. In particular, immune checkpoint inhibitors (ICIs) that target and inhibit programmed cell death-1 (PD-1) and programmed cell death ligand-1 (PD-L1), have shown promising results in the treatment of patients with metastatic TNBC. However, while manipulating the immune system to induce antitumor response, ICIs can also lead to a unique set of immune-related adverse events (IRAEs), which differ from standard chemotherapy toxicities due to their immune-based origin. These toxicities require highly specific management, including guidance from multidisciplinary specialists. The primary treatment strategy against IRAEs is systemic corticosteroid use, but additional treatment approaches may also involve supportive care, additional immunosuppression, and concurrent treatment delay or discontinuation. Given the rising prevalence of ICI therapy, it is essential to educate clinicians on the presentation and management of these potentially life-threatening events so that they are identified early and treated appropriately. Using data from recent clinical trials, this review will focus on known IRAEs, particularly those seen in patients with breast cancer, and will summarize their prevalence, severity, and outcomes. We will discuss optimal strategies for early recognition and management, as well as approaches toward cautious retreatment following resolution of IRAEs.

摘要

免疫疗法的广泛应用已经彻底改变了各种癌症类型的治疗方法,包括转移性三阴性乳腺癌(TNBC),这种癌症长期以来一直与预后不良相关。特别是,针对程序性细胞死亡蛋白-1(PD-1)和程序性细胞死亡配体-1(PD-L1)的免疫检查点抑制剂(ICIs)在治疗转移性 TNBC 患者方面显示出了有前途的结果。然而,虽然操纵免疫系统以诱导抗肿瘤反应,但 ICIs 也可能导致一组独特的免疫相关不良事件(IRAEs),这些不良事件与标准化疗毒性不同,因为它们源于免疫。这些毒性需要高度特异性的管理,包括多学科专家的指导。针对 IRAEs 的主要治疗策略是使用全身性皮质类固醇,但其他治疗方法可能还包括支持性护理、额外的免疫抑制以及同时延迟或停止治疗。鉴于 ICIs 治疗的流行率不断上升,教育临床医生识别和管理这些潜在危及生命的事件至关重要,以便及早识别并进行适当治疗。本综述将使用最近临床试验的数据,重点关注已知的 IRAEs,特别是在乳腺癌患者中出现的 IRAEs,并总结它们的发生率、严重程度和结果。我们将讨论早期识别和管理的最佳策略,以及在 IRAEs 解决后谨慎重新治疗的方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0456/8841316/9ed836cfd5b8/10549_2021_6480_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0456/8841316/9ed836cfd5b8/10549_2021_6480_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0456/8841316/9ed836cfd5b8/10549_2021_6480_Fig1_HTML.jpg

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