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免疫检查点抑制剂诱导(3 型)自身免疫性胰腺炎。

Immune Checkpoint Inhibitor-Induced (Type 3) Autoimmune Pancreatitis.

机构信息

University of Texas MD Anderson Cancer Center, Houston, TX, USA.

Department of Internal Medicine, Division of Gastroenterology, Hepatology and Nutrition, University of Texas MD Anderson Cancer Center, 1515 Holcombe Blvd, Houston, TX, 77030, USA.

出版信息

Curr Gastroenterol Rep. 2023 Oct;25(10):255-259. doi: 10.1007/s11894-023-00885-6. Epub 2023 Oct 17.

DOI:10.1007/s11894-023-00885-6
PMID:37845557
Abstract

PURPOSE OF REVIEW

Immune checkpoint inhibitors (ICI) have revolutionized cancer care and work primarily by blocking CTLA-4 (cytotoxic T-lymphocyte-associated protein 4), and/or PD-1 (programmed cell death protein 1), and/or PD-L1 (programmed death-ligand 1), thereby providing highly efficacious anti-tumor activity. However, this unmitigated immune response can also trigger immune related adverse events (irAEs) in multiple organs, with pancreatic irAEs (now referred to as type 3 Autoimmune pancreatitis (AIP) being infrequent.

RECENT FINDINGS

Type 3 AIP is a drug-induced, immune mediated progressive inflammatory disease of the pancreas that may have variable clinical presentations viz., an asymptomatic pancreatic enzyme elevation, incidental imaging evidence of pancreatitis, painful pancreatitis, or any combination of these subtypes. Management is largely supportive with intravenous fluid hydration, pain control and holding the inciting medication. Steroids have not been shown to demonstrate a clear benefit in acute management. A rapid development pancreatic atrophy is observed on imaging as early as 1 year post initial injury. Type 3 AIP is a chronic inflammatory disease of the pancreas that though predominantly asymptomatic and mild in severity can lead to rapid organ volume loss regardless of type of clinical presentation and despite steroid therapy.

摘要

目的综述

免疫检查点抑制剂(ICI)改变了癌症治疗方式,主要通过阻断 CTLA-4(细胞毒性 T 淋巴细胞相关蛋白 4)和/或 PD-1(程序性细胞死亡蛋白 1)和/或 PD-L1(程序性死亡配体 1),从而提供高效的抗肿瘤活性。然而,这种不受控制的免疫反应也会在多个器官引发免疫相关不良反应(irAEs),胰腺 irAEs(现在称为 3 型自身免疫性胰腺炎(AIP))并不常见。

最近的发现

3 型 AIP 是一种药物诱导的、免疫介导的胰腺进行性炎症性疾病,其临床表现可能多种多样,如无症状的胰腺酶升高、偶然发现的胰腺炎影像学证据、胰腺炎疼痛或这些亚型的任何组合。治疗主要是支持性的,包括静脉补液、止痛和停用引发疾病的药物。皮质类固醇在急性治疗中并没有显示出明显的益处。在初始损伤后 1 年内,影像学上可观察到胰腺迅速萎缩。3 型 AIP 是一种慢性胰腺炎症性疾病,尽管主要无症状且病情较轻,但无论临床表现类型如何,即使进行皮质类固醇治疗,也会导致快速的器官体积丧失。

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Front Immunol. 2022 Apr 26;13:779691. doi: 10.3389/fimmu.2022.779691. eCollection 2022.
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Association between immune-related adverse event timing and treatment outcomes.免疫相关不良事件发生时间与治疗结局的相关性。
Oncoimmunology. 2022 Jan 5;11(1):2017162. doi: 10.1080/2162402X.2021.2017162. eCollection 2022.
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Clinical and Hematological Predictors of High-Grade Immune-Related Adverse Events Associated With Immune Checkpoint Inhibitors.
Investigating Immune Checkpoint Inhibitor-Induced Pancreatic Injury: When to Discontinue Cancer Therapy.
探究免疫检查点抑制剂诱导的胰腺损伤:何时停止癌症治疗。
Metabolites. 2025 Jun 10;15(6):385. doi: 10.3390/metabo15060385.
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Autoimmune Pancreatitis: A Review.自身免疫性胰腺炎:综述
J Clin Med. 2025 Apr 29;14(9):3076. doi: 10.3390/jcm14093076.
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HOMA-beta independently predicts survival in patients with advanced cancer on treatment with immune checkpoint inhibitors.稳态模型评估的β细胞功能指数(HOMA-β)可独立预测接受免疫检查点抑制剂治疗的晚期癌症患者的生存率。
Front Endocrinol (Lausanne). 2024 Dec 11;15:1439705. doi: 10.3389/fendo.2024.1439705. eCollection 2024.
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Systematic review of immune checkpoint inhibitor-related gastrointestinal, hepatobiliary, and pancreatic adverse events.免疫检查点抑制剂相关的胃肠道、肝胆和胰腺不良事件的系统评价。
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