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Collateral Damage: Insulin-Dependent Diabetes Induced With Checkpoint Inhibitors

机译:附带损害:检查点抑制剂引起的胰岛素依赖型糖尿病

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摘要

Insulin-dependent diabetes may occur in patients with cancers who are treated with checkpoint inhibitors (CPIs). We reviewed cases occurring over a 6-year period at two academic institutions and identified 27 patients in whom this developed, or an incidence of 0.9%. The patients had a variety of solid-organ cancers, but all had received either anti-PD-1 or anti-PD-L1 antibodies. Diabetes presented with ketoacidosis in 59%, and 42% had evidence of pancreatitis in the peridiagnosis period. Forty percent had at least one positive autoantibody and 21 % had two or more. There was a predominance of HLA-DR4, which was present in 76% of patients. Other immune adverse events were seen in 70%, and endocrine adverse events in 44%. We conclude that autoimmune, insulin-dependent diabetes occurs in close to 1% of patients treated with anti-PD-1 or -PD-L1 CPIs. This syndrome has similarities and differences compared with classic type 1 diabetes. The dominance of HLA-DR4 suggests an opportunity to identify those at highest risk of these complications and to discover insights into the mechanisms of this adverse event.
机译:接受检查点抑制剂(CPI)治疗的癌症患者可能会出现胰岛素依赖型糖尿病。我们回顾了两个学术机构在6年内发生的病例,并确定了其中27例发生这种情况的患者,发生率为0.9%。这些患者患有多种实体器官癌,但均接受了抗PD-1或抗PD-L1抗体。糖尿病患者中有酮症酸中毒的占59%,有42%的患者在围诊期有胰腺炎的迹象。 40%的人至少有一种阳性自身抗体,而21%的人有两种或更多。 HLA-DR4占优势,在76%的患者中存在。其他免疫不良事件的发生率为70%,内分泌不良事件的发生率为44%。我们得出的结论是,接受抗PD-1或-PD-L1 CPI治疗的患者中,近1%会发生自身免疫性胰岛素依赖型糖尿病。与经典的1型糖尿病相比,该综合征具有异同。 HLA-DR4的优势表明,有机会确定那些并发症风险最高的人,并了解这种不良事件的机制。

著录项

  • 来源
    《Diabetes》 |2018年第8期|1471-1480|共10页
  • 作者单位

    Section of Endocrinology and Metabolism, Department of Internal Medicine, Yale University, New Haven, CT;

    Division of Endocrinology and Metabolism, Department of Medicine, University of California, San Francisco, San Francisco, CA;

    Section of Endocrinology and Metabolism, Department of Internal Medicine, Yale University, New Haven, CT;

    Department of Immunobiology, Yale University, New Haven, CT;

    Section of Medical Oncology, Department of Internal Medicine, Yale University, New Haven, CT;

    Section of Medical Oncology, Department of Internal Medicine, Yale University, New Haven, CT;

    Section of Medical Oncology, Department of Internal Medicine, Yale University, New Haven, CT;

    Section of Medical Oncology, Department of Internal Medicine, Yale University, New Haven, CT;

    Division of Endocrinology and Metabolism, Department of Medicine, University of California, San Francisco, San Francisco, CA;

    Division of Endocrinology and Metabolism, Department of Medicine, University of California, San Francisco, San Francisco, CA;

    Division of Hematology and Oncology, University of California, San Francisco, San Francisco, CA;

    Division of Endocrinology and Metabolism, Department of Medicine, University of California, San Francisco, San Francisco, CA,Parker Institute for Cancer Immunotherapy, San Francisco, CA;

    Division of Endocrinology and Metabolism, Department of Medicine, University of California, San Francisco, San Francisco, CA;

    Section of Endocrinology and Metabolism, Department of Internal Medicine, Yale University, New Haven, CT,Department of Immunobiology, Yale University, New Haven, CT;

  • 收录信息 美国《科学引文索引》(SCI);美国《化学文摘》(CA);
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
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  • 入库时间 2022-08-18 03:46:02

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