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免疫检查点抑制剂相关的免疫不良反应

[Immune-related adverse events by immune checkpoint inhibitors].

作者信息

Kadono Takafumi

机构信息

Department of Dermatology, St. Marianna University School of Medicine.

出版信息

Nihon Rinsho Meneki Gakkai Kaishi. 2017;40(2):83-89. doi: 10.2177/jsci.40.83.

Abstract

Recent introduction of immune checkpoint inhibitors represented by anti-PD-1 antibodies such as nivolumab and pembrolizumab, and anti-CTLA-4 antibody such as ipilimumab had a great impact on cancer immunotherapy especially for melanoma, non-small cell lung cancer, renal cell carcinoma, and Hodgkin's lymphoma. On the other hand, immune checkpoint inhibitors have their own distinctive adverse events, which are collectively named as "immune-related adverse events". Although immune-related adverse events may occur at any part of the body, interstitial pneumonia, colitis, hypothyroidism, liver dysfunction, skin rash, vitiligo, hypophysitis, type 1 diabetes, renal dysfunction, myasthenia gravis, neuropathy, myositis, and uveitis are representative. The onset of these immune-related adverse events varies. As for ipilimumab, cutaneous and mucous complications appear relatively early, and subsequently digestive symptoms emerge. As for nivolumab, most immune-related adverse events start around a few months after its administration. These immune-related adverse events are basically managed according to the algorism. Prompt consultation to the experts are of great importance and the grade of immune-related adverse events and patients' disease conditions need to be carefully evaluated to decide the optimal measures. As immune-related adverse events could affect various organs, cooperation with many experts from various fields is critical and it is important to organize a cooperative system within a hospital.

摘要

以纳武单抗和派姆单抗等抗PD - 1抗体以及伊匹单抗等抗CTLA - 4抗体为代表的免疫检查点抑制剂的近期问世,对癌症免疫治疗产生了重大影响,尤其是对黑色素瘤、非小细胞肺癌、肾细胞癌和霍奇金淋巴瘤。另一方面,免疫检查点抑制剂有其独特的不良事件,这些不良事件统称为“免疫相关不良事件”。尽管免疫相关不良事件可能发生在身体的任何部位,但间质性肺炎、结肠炎、甲状腺功能减退、肝功能障碍、皮疹、白癜风、垂体炎、1型糖尿病、肾功能障碍、重症肌无力、神经病变、肌炎和葡萄膜炎是其代表。这些免疫相关不良事件的发病情况各不相同。就伊匹单抗而言,皮肤和黏膜并发症出现相对较早,随后出现消化系统症状。就纳武单抗而言,大多数免疫相关不良事件在给药后几个月左右开始出现。这些免疫相关不良事件基本上按照算法进行处理。及时咨询专家非常重要,需要仔细评估免疫相关不良事件的分级和患者的病情,以决定最佳措施。由于免疫相关不良事件可能影响多个器官,与来自各个领域的众多专家合作至关重要,在医院内组织一个合作系统也很重要。

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