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一例无胰岛自身抗体的快速进展型胰岛素依赖型糖尿病在首次使用纳武单抗两年后出现。

A case of rapidly progressive insulin-dependent diabetes mellitus without islet autoantibodies developed over two years after the first dose of nivolumab.

作者信息

Nishihama Kota, Okano Yuko, Inoue Chisa, Maki Kanako, Eguchi Kazuhito, Tanaka Soichiro, Takeshita Atsuro, Uemura Mei, Yasuma Taro, Suzuki Toshinari, Gabazza Esteban C, Yano Yutaka

机构信息

Department of Diabetes, Metabolism, and Endocrinology, Mie University Graduate School of Medicine, 2-174 Edobashi, Tsu City, Mie 514-8507 Japan.

Department of Immunology, Mie University Graduate School of Medicine, Tsu, Japan.

出版信息

Diabetol Int. 2024 Mar 11;15(3):583-588. doi: 10.1007/s13340-024-00703-y. eCollection 2024 Jul.

DOI:10.1007/s13340-024-00703-y
PMID:39101192
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11291771/
Abstract

The case was an 80-year-old Japanese man. He was diagnosed with right renal cell carcinoma when he was 74. After laparoscopic radical nephrectomy, the patient received interferon, sorafenib, axitinib, and nivolumab therapy. The patient developed rapid progressive insulin-dependent diabetes mellitus (DM) after 46 courses of nivolumab monotherapy (772 days from the first nivolumab treatment). Glutamic acid decarboxylase antibody, islet cell cytoplasmic antibody, islet cell antigen-2 antibody, insulin antibody, and zinc transporter 8 antibody were all negative. Human leukocyte antigen (HLA) typing showed DRB1*09:01, DRB1 13:02, DQB103:03, and DQB1 *06:04. Multiple daily insulin injections were started. However, controlling his blood glucose by standard multiple daily insulin injection treatments was difficult. The patient survived more than two years after the onset of immune checkpoint inhibitor-associated DM (ICI-DM). This is a valuable report of late-onset ICI-DM with a detailed patient background and clinical course over two years after the first dose of nivolumab.

摘要

该病例为一名80岁的日本男性。他在74岁时被诊断为右肾细胞癌。在接受腹腔镜根治性肾切除术后,患者接受了干扰素、索拉非尼、阿昔替尼和纳武单抗治疗。在接受46个疗程的纳武单抗单药治疗后(自首次使用纳武单抗治疗起772天),患者出现了快速进展的胰岛素依赖型糖尿病(DM)。谷氨酸脱羧酶抗体、胰岛细胞胞浆抗体、胰岛细胞抗原2抗体、胰岛素抗体和锌转运体8抗体均为阴性。人类白细胞抗原(HLA)分型显示为DRB1*09:01、DRB1 13:02、DQB103:03和DQB1 *06:04。开始每日多次注射胰岛素。然而,通过标准的每日多次胰岛素注射治疗来控制他的血糖很困难。该患者在免疫检查点抑制剂相关糖尿病(ICI-DM)发病后存活了两年多。这是一份关于迟发性ICI-DM的有价值报告,详细介绍了患者背景和自首次使用纳武单抗起两年多的临床病程。

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本文引用的文献

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Type 1 diabetes mellitus affected by potential toxicity from long-term use of nivolumab.1型糖尿病受长期使用纳武单抗潜在毒性影响。
Diabetol Int. 2023 Aug 28;15(1):130-134. doi: 10.1007/s13340-023-00659-5. eCollection 2024 Jan.
2
Risk Factors and Characteristics of Checkpoint Inhibitor-Associated Autoimmune Diabetes Mellitus (CIADM): A Systematic Review and Delineation From Type 1 Diabetes.风险因素和检查点抑制剂相关自身免疫性糖尿病(CIADM)的特征:一项系统评价,并与 1 型糖尿病相区别。
Diabetes Care. 2023 Jun 1;46(6):1292-1299. doi: 10.2337/dc22-2202.
3
Society for Immunotherapy of Cancer (SITC) consensus definitions for immune checkpoint inhibitor-associated immune-related adverse events (irAEs) terminology.癌症免疫治疗学会(SITC)免疫检查点抑制剂相关免疫相关不良事件(irAEs)术语的共识定义。
J Immunother Cancer. 2023 Mar;11(3). doi: 10.1136/jitc-2022-006398.
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Risk factors for severe immune-related adverse events after first-line pembrolizumab monotherapy or combination chemotherapy for non-small-cell lung cancer.一线帕博利珠单抗单药或联合化疗治疗非小细胞肺癌后发生严重免疫相关不良事件的风险因素。
Invest New Drugs. 2022 Dec;40(6):1298-1305. doi: 10.1007/s10637-022-01310-x. Epub 2022 Oct 13.
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Immune cells and their inflammatory mediators modify β cells and cause checkpoint inhibitor-induced diabetes.免疫细胞及其炎症介质可修饰β细胞,并导致检查点抑制剂诱导的糖尿病。
JCI Insight. 2022 Sep 8;7(17):e156330. doi: 10.1172/jci.insight.156330.
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