Immune checkpoint inhibitors-induced pancreatitis: a systematic review and real-world pharmacovigilance analysis.

IF 4.4 2区 医学 Q1 PHARMACOLOGY & PHARMACY
Frontiers in Pharmacology Pub Date : 2025-03-19 eCollection Date: 2025-01-01 DOI:10.3389/fphar.2025.1426847
Wei Fang, Huanping Wang, Xiaoran Zhang, Hongxia Zhu, Wei Yan, Yang Gao
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引用次数: 0

Abstract

Purpose: Immune checkpoint inhibitors-induced pancreatitis (ICIs-P) is an uncommon immune-related adverse event. The available evidence consists mostly of case reports, case series, and narrative reviews. This research focuses on the clinical characteristics and management options for ICIs-P to provide a practice-based global perspective on this disease.

Methods: Five electronic databases were systematically reviewed to identify the relevant studies. Furthermore, we performed a disproportionality analysis utilizing OpenVigil 2.1 to interrogate the United States Food and Drug Administration's Adverse Event Reporting System (FAERS) database.

Results: A total of 61 patients from 58 studies were included in this study. Most patients with ICIs-P were males (60.7%). Most patients received anti-PD-1/PD-L1 monotherapy (78.7%) or anti-PD-1/PD-L1 monotherapy in conjunction with CTLA-4 blockade (19.7%). The median time from the initiation of immune checkpoint inhibitors treatment to pancreatitis was 108 days (range 52-278). Most cases were severe or life-threatening (G3-G4; 64.0%). Corticosteroids were administered to 73.8% of the patients during the treatment of pancreatitis. Regarding treatment outcomes, ICIs-P was reversible in most cases (83.6%), despite the 8.2% relapse and 8.2% deaths. We identified 606 reports of pancreatitis associated with ICIs in the FAERS database, with the greatest proportion of males (50.7%), 62.0% of PD-1 inhibitors, and 22.1% of all reports of death or life-threatening outcomes. Signals indicating pancreatitis were observed across all ICIs, with particular emphasis on Cemiplimab, Pembrolizumab and Nivolumab.

Conclusion: By using a pharmacovigilance database, we discovered an elevated risk of pancreatitis following ICIs therapy, especially with PD-1 inhibitors. Meanwhile, risk factors for ICIs-P remain poorly understood, and diagnosis is challenging. Which may manifest as asymptomatic elevated pancreatic enzyme levels or clinical pancreatitis. Patients with pancreatitis symptoms should have their lipase and amylase levels and radiology evaluated. Diagnosis should be made by excluding other causes. Steroids are the cornerstone of ICIs-P treatment and slow dose reduction is recommended to reduce recurrence.

免疫检查点抑制剂诱导的胰腺炎:系统回顾和现实世界的药物警戒分析。
目的:免疫检查点抑制剂诱导的胰腺炎(ICIs-P)是一种罕见的免疫相关不良事件。现有的证据主要包括病例报告、病例系列和叙述性评论。本研究的重点是ICIs-P的临床特征和管理选择,为这种疾病提供基于实践的全球视角。方法:系统检索5个电子数据库,筛选相关研究。此外,我们利用OpenVigil 2.1查询美国食品和药物管理局的不良事件报告系统(FAERS)数据库进行了歧化分析。结果:58项研究共纳入61例患者。ICIs-P患者以男性为主(60.7%)。大多数患者接受抗pd -1/PD-L1单药治疗(78.7%)或抗pd -1/PD-L1单药治疗联合CTLA-4阻断(19.7%)。从开始免疫检查点抑制剂治疗到胰腺炎的中位时间为108天(范围52-278)。大多数病例严重或危及生命(G3-G4;64.0%)。在胰腺炎治疗期间,73.8%的患者使用了皮质类固醇。关于治疗结果,尽管有8.2%的复发和8.2%的死亡,但大多数病例(83.6%)的ICIs-P是可逆的。我们在FAERS数据库中确定了606例与ICIs相关的胰腺炎报告,其中男性的比例最大(50.7%),PD-1抑制剂的比例为62.0%,死亡或危及生命的结果占所有报告的22.1%。在所有ici中观察到胰腺炎信号,特别强调塞米普利单抗、派姆单抗和尼武单抗。结论:通过使用药物警戒数据库,我们发现ICIs治疗后胰腺炎的风险增加,特别是使用PD-1抑制剂。与此同时,ICIs-P的危险因素仍然知之甚少,诊断具有挑战性。可能表现为无症状胰酶水平升高或临床胰腺炎。有胰腺炎症状的患者应检查其脂肪酶和淀粉酶水平和放射学。诊断应排除其他原因。类固醇是ICIs-P治疗的基础,建议缓慢减少剂量以减少复发。
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来源期刊
Frontiers in Pharmacology
Frontiers in Pharmacology PHARMACOLOGY & PHARMACY-
CiteScore
7.80
自引率
8.90%
发文量
5163
审稿时长
14 weeks
期刊介绍: Frontiers in Pharmacology is a leading journal in its field, publishing rigorously peer-reviewed research across disciplines, including basic and clinical pharmacology, medicinal chemistry, pharmacy and toxicology. Field Chief Editor Heike Wulff at UC Davis is supported by an outstanding Editorial Board of international researchers. This multidisciplinary open-access journal is at the forefront of disseminating and communicating scientific knowledge and impactful discoveries to researchers, academics, clinicians and the public worldwide.
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