Co-Chair of Task Force, Barrow Neurological Institute, Department of Medicine, University of Arizona College of Medicine and Creighton School of Medicine, Phoenix, Arizona.
Co-Chair of Task Force, Division of Endocrinology, Diabetes and Metabolism, Mayo Clinic, Jacksonville, Florida.
Endocr Pract. 2022 Jul;28(7):719-731. doi: 10.1016/j.eprac.2022.04.010. Epub 2022 Apr 25.
The aim of this case-based clinical review was to provide a practical approach for clinicians regarding the management of patients with immune checkpoint inhibitor (ICI)-mediated endocrinopathies.
A literature search of PubMed, Embase, and Scopus was conducted using appropriate keywords. The discussions and strategies for the diagnosis and management of ICI-mediated endocrinopathies are based on evidence available from prospective, randomized clinical studies; cohort studies; cross-sectional studies; case-based studies; and an expert consensus.
Immunotherapy with ICIs has transformed the treatment landscape of diverse types of cancers but frequently results in immune-mediated endocrinopathies that can cause acute and persistent morbidity and, rarely, death. The patterns of endocrinopathies differ between the inhibitors of the cytotoxic T-lymphocyte antigen 4 and programmed cell death protein 1 or programmed cell death protein 1 ligand pathways but most often involve the thyroid and pituitary glands. The less common but important presentations include insulin-deficient diabetes mellitus, primary adrenal insufficiency, primary hypoparathyroidism, central diabetes insipidus, primary hypogonadism, and pancreatitis, with or without subsequent progression to diabetes mellitus or exocrine insufficiency.
In recent years, with increasing numbers of patients with cancer being treated with ICIs, more clinicians in a variety of specialties have been called upon to diagnose and treat ICI-mediated endocrinopathies. Herein, we reviewed case scenarios of various clinical manifestations and emphasized the need for a high index of clinical suspicion by all clinicians caring for these patients, including endocrinologists, oncologists, primary care providers, and emergency department physicians. We also provided diagnostic and therapeutic approaches for ICI-induced endocrinopathies and proposed that patients on ICI therapy be evaluated and treated by a multidisciplinary team in collaboration with endocrinologists.
本基于病例的临床综述旨在为临床医生提供一种实用方法,用于管理免疫检查点抑制剂(ICI)介导的内分泌疾病患者。
使用适当的关键词在 PubMed、Embase 和 Scopus 上进行文献检索。ICI 介导的内分泌疾病的诊断和管理讨论和策略基于来自前瞻性、随机临床试验;队列研究;横断面研究;基于病例的研究;和专家共识的现有证据。
ICI 的免疫疗法改变了多种类型癌症的治疗格局,但经常导致免疫介导的内分泌疾病,可导致急性和持续性发病,并且很少导致死亡。抑制剂的内分泌疾病模式不同细胞毒性 T 淋巴细胞抗原 4 和程序性细胞死亡蛋白 1 或程序性细胞死亡蛋白 1 配体途径,但最常涉及甲状腺和垂体。不太常见但重要的表现包括胰岛素缺乏型糖尿病、原发性肾上腺功能不全、原发性甲状旁腺功能减退症、中枢性尿崩症、原发性性腺功能减退症和胰腺炎,伴有或不伴有随后进展为糖尿病或外分泌功能不全。
近年来,随着越来越多的癌症患者接受 ICI 治疗,越来越多的各种专业的临床医生被要求诊断和治疗 ICI 介导的内分泌疾病。在此,我们回顾了各种临床表现的病例情景,并强调了所有照顾这些患者的临床医生(包括内分泌学家、肿瘤学家、初级保健提供者和急诊医生)都需要高度的临床怀疑。我们还为 ICI 诱导的内分泌疾病提供了诊断和治疗方法,并提出建议ICI 治疗的患者应与内分泌学家合作,由多学科团队进行评估和治疗。