Immunomodulators and advanced therapies for maintenance of remission in Crohn's disease: systematic review and network meta-analysis.

IF 3.8 3区 医学 Q1 GASTROENTEROLOGY & HEPATOLOGY
Therapeutic Advances in Gastroenterology Pub Date : 2026-07-27 eCollection Date: 2026-01-01 DOI:10.1177/17562848261470683
Vassiliki Sinopoulou, Morris Gordon, Shiyao Liu, Daniel Arruda Navarro Albuquerque, Aderonke Ajiboye, Sudheer Kumar Vuyyuru, Shellie Jane Radford, Gordon William Moran
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引用次数: 0

Abstract

Background: With the range of options available for the treatment of Crohn's disease, therapy selection can be challenging in clinical practice. Comparative efficacy data are needed to clarify the relative position of the increasingly complex portfolio of advanced therapies and guide decision-making.

Objectives: Our aim was to compare all advanced and immunomodulator treatments for efficacy and safety in maintenance of remission.

Design: Systematic review and network meta-analysis.

Data sources and methods: We searched databases up to June 2025. Our outcomes were clinical relapse, loss of response, endoscopic relapse, and safety outcomes. We estimated risk ratio (RR) and 95% confidence interval (CI). We used GRADE to assess certainty of results, and surface under the cumulative ranking curve for ranking treatments.

Results: A total of 37 randomised controlled trials with 7415 participants were included. Interventions ranged between 22 weeks and 2 years. Adalimumab probably prevents clinical relapse over placebo (RR 0.68, 95% CI 0.54-0.84, Number Needed to Treat (NNT) = 2, moderate effect magnitude). CT-P13 (RR 0.52, 95% CI 0.38-0.71) and infliximab (RR 0.61, 95% CI 0.49-0.76) may prevent clinical relapse. Upadacitinib is more effective than placebo at preventing loss of clinical response (RR 0.64, 95% CI 0.57-0.72, NNT = 2, small magnitude), while CT-P13 (RR 0.46, 95% CI 0.35-0.53, NNT = 1, large magnitude), natalizumab (RR 0.54, 95% CI 0.43-0.68, NNT = 2, moderate magnitude), certolizumab (RR 0.57, 95% CI 0.47-0.7), NNT = 2, moderate magnitude), adalimumab (RR 0.68, 95% CI 0.61-0.75, NNT = 2, small effect magnitude) and ustekinumab (RR 0.73, 95% CI 0.61-0.86, NNT = 2, small magnitude) probably prevent loss of clinical response. Infliximab (RR 0.7, 95% CI 0.59-0.82) and vedolizumab (RR 0.82, 95% CI 0.68-0.99) may prevent loss of clinical response. Endoscopic relapse could not be analysed. Safety evidence is uncertain, but treatments appear generally safe in the short term.

Conclusion: Adalimumab has moderate certainty for maintaining clinical remission with a moderate effect size. Novel therapies seem to have similar effect sizes, though imprecision due to limited evidence precludes further conclusions.

Trial registration: https://knowledge.lancashire.ac.uk/id/eprint/53237/.

克罗恩病维持缓解的免疫调节剂和先进疗法:系统评价和网络荟萃分析
背景:随着治疗克罗恩病的选择范围,治疗选择在临床实践中可能具有挑战性。需要比较疗效数据来明确日益复杂的先进疗法组合的相对位置并指导决策。目的:我们的目的是比较所有先进和免疫调节治疗在维持缓解的有效性和安全性。设计:系统评价和网络荟萃分析。数据来源和方法:检索截至2025年6月的数据库。我们的结果是临床复发、反应丧失、内镜下复发和安全性结果。我们估计了风险比(RR)和95%置信区间(CI)。我们使用GRADE来评估结果的确定性,并在累积排名曲线下显示对治疗的排名。结果:共纳入37项随机对照试验,7415名受试者。干预时间从22周到2年不等。阿达木单抗可能比安慰剂预防临床复发(RR 0.68, 95% CI 0.54-0.84,需要治疗的人数(NNT) = 2,中等效果)。CT-P13 (RR 0.52, 95% CI 0.38-0.71)和英夫利昔单抗(RR 0.61, 95% CI 0.49-0.76)可预防临床复发。Upadacitinib在预防临床反应丧失方面比安慰剂更有效(RR 0.64, 95% CI 0.57-0.72, NNT = 2,小量级),而CT-P13 (RR 0.46, 95% CI 0.35-0.53, NNT = 1,大量级)、natalizumab (RR 0.54, 95% CI 0.43-0.68, NNT = 2,中等量级)、certolizumab (RR 0.57, 95% CI 0.47-0.7), NNT = 2,中等量级)、阿达木单抗(RR 0.68, 95% CI 0.61-0.75, NNT = 2,小量级)和ustekinumab (RR 0.73, 95% CI 0.61-0.86, NNT = 2,小幅度)可能防止临床反应的丧失。英夫利昔单抗(RR = 0.7, 95% CI 0.59-0.82)和维多单抗(RR = 0.82, 95% CI 0.68-0.99)可以预防临床反应的丧失。内镜下复发无法分析。安全性证据尚不确定,但治疗在短期内通常是安全的。结论:阿达木单抗在维持临床缓解方面具有中等确定性,效应大小中等。新的治疗方法似乎具有类似的效果大小,尽管由于证据有限而不精确,因此无法进一步得出结论。试验注册:https://knowledge.lancashire.ac.uk/id/eprint/53237/。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Therapeutic Advances in Gastroenterology
Therapeutic Advances in Gastroenterology GASTROENTEROLOGY & HEPATOLOGY-
CiteScore
6.70
自引率
2.40%
发文量
103
审稿时长
15 weeks
期刊介绍: Therapeutic Advances in Gastroenterology is an open access journal which delivers the highest quality peer-reviewed original research articles, reviews, and scholarly comment on pioneering efforts and innovative studies in the medical treatment of gastrointestinal and hepatic disorders. The journal has a strong clinical and pharmacological focus and is aimed at an international audience of clinicians and researchers in gastroenterology and related disciplines, providing an online forum for rapid dissemination of recent research and perspectives in this area. The editors welcome original research articles across all areas of gastroenterology and hepatology. The journal publishes original research articles and review articles primarily. Original research manuscripts may include laboratory, animal or human/clinical studies – all phases. Letters to the Editor and Case Reports will also be considered.
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