Systematic review: colitis associated with anti-CTLA-4 therapy

医学 易普利姆玛 银耳霉素 英夫利昔单抗 结肠炎 不利影响 内科学 免疫学 中止 CTLA-4号机组 溃疡性结肠炎 免疫疗法 胃肠病学 免疫系统 癌症 T细胞 肿瘤坏死因子α 疾病
作者
Arjun Gupta,Kara M. De Felice,Edward V. Loftus,Sahil Khanna
出处
期刊:Alimentary Pharmacology & Therapeutics [Wiley]
卷期号:42 (4): 406-417 被引量:254
标识
DOI:10.1111/apt.13281
摘要

Summary Background Cytotoxic T‐lymphocyte‐associated protein‐4 ( CTLA ‐4) has an important role in T‐cell regulation, proliferation and tolerance. Anti‐ CTLA ‐4 agents, such as ipilimumab and tremelimumab, have been shown to prolong overall survival in patients with metastatic melanoma, and their use is being investigated in the treatment of other malignancies. Their novel immunostimulatory mechanism, however, predisposes patients to immune‐related adverse effects, of which gastrointestinal effects such as diarrhoea and colitis are the most common. Aims To discuss the existing literature and summarise the epidemiology, pathogenesis and clinical features of anti‐ CTLA ‐4‐associated colitis, and to present a management algorithm for it. Methods We searched PubMed for studies published through October 2014 using the terms ‘anti‐ CTLA ,’ ‘ipilimumab,’ ‘tremelimumab,’ ‘colitis,’ ‘gastrointestinal,’ ‘immune‐related adverse effect,’ ‘immunotherapy,’ ‘melanoma,’ and ‘diarrhoea.’ Results Watery diarrhoea is commonly associated with anti‐ CTLA ‐4 therapy (27–54%), and symptoms occur within a few days to weeks of therapy. Diffuse acute and chronic colitis are the most common findings on endoscopy (8–22%). Concomitant infectious causes of diarrhoea must be evaluated. Most cases may be successfully managed with discontinuation of anti‐ CTLA ‐4 and conservative therapy. Those with persistent grade 2 and grade 3/4 diarrhoea should undergo endoscopic evaluation and require corticosteroid therapy. Corticosteroid‐resistant cases may respond to anti‐tumour necrosis factor‐alpha therapy such as infliximab. Surgery is reserved for patients with bowel perforation or failure of medical therapy. Conclusion Given the increasing use of anti‐ CTLA ‐4 therapy, clinicians must be aware of related adverse events and their management.
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