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自身免疫性糖尿病和甲状腺炎使纳武单抗治疗复杂化。

Autoimmune Diabetes and Thyroiditis Complicating Treatment with Nivolumab.

作者信息

Li Li, Masood Awais, Bari Shahla, Yavuz Sahzene, Grosbach Alan B

机构信息

aDivision of Hematology and Oncology, Department of Medicine, University of Florida, Gainesville, Florida, USA.

dDivision of Hematology and Oncology, Malcom Randall VA Medical Center, Gainesville, Florida, USA.

出版信息

Case Rep Oncol. 2017 Mar 2;10(1):230-234. doi: 10.1159/000456540. eCollection 2017 Jan-Apr.

Abstract

Programmed cell death-1 (PD-1) ligand inhibitors have gained popularity in the treatment of advanced non-small-cell lung cancer. The immune system is regulated by stimulatory and inhibitory signaling and aims to achieve the balance between activation and inhibition. Treatment with immune checkpoint inhibitors enhances immune response, but is also known to diminish immune tolerance and increase autoimmune toxicity. Here we present a case of a patient with advanced squamous cell lung cancer who developed type I diabetes and thyroiditis after treatment with PD-1 checkpoint inhibitor nivolumab. The presence of autoimmune diabetes mellitus and thyroiditis were confirmed by markedly elevated titers of the glutamic acid decarboxylase autoantibody and thyroid peroxidase antibody, respectively. This report serves to heighten awareness of potential autoimmune toxicities related to anti-PD-1 therapy, especially as these toxicities are manageable if identified in a timely manner.

摘要

程序性细胞死亡蛋白1(PD-1)配体抑制剂在晚期非小细胞肺癌的治疗中已受到广泛关注。免疫系统由刺激性和抑制性信号调节,旨在实现激活与抑制之间的平衡。免疫检查点抑制剂治疗可增强免疫反应,但也会降低免疫耐受性并增加自身免疫毒性。在此,我们报告一例晚期鳞状细胞肺癌患者,在接受PD-1检查点抑制剂纳武单抗治疗后发生了I型糖尿病和甲状腺炎。自身免疫性糖尿病和甲状腺炎的存在分别通过谷氨酸脱羧酶自身抗体和甲状腺过氧化物酶抗体滴度显著升高得以证实。本报告旨在提高对与抗PD-1治疗相关的潜在自身免疫毒性的认识,特别是如果能及时发现,这些毒性是可控的。

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