Efficacy and safety of medical therapies in microscopic colitis: a systematic review and network meta-analysis.

Aditi Kumar, George Hiner, Matthew J Brookes, Jonathan P Segal
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Abstract

Background: The mainstay of treatment for microscopic colitis (MC) is budesonide. However, the optimal formulation and dosage of budesonide to induce and maintain remission has not yet been clearly demonstrated.

Objectives: To compare the data for efficacy and safety of treatments to induce and maintain remission for MC.

Design: We conducted a meta-analysis of randomised controlled trials (RCTs) comparing treatment with each other or placebo for induction and maintenance of clinical and histological remission in MC.

Data sources and methods: We searched MEDLINE (1946 to May 2021), EMBASE and EMBASE Classis (1947 to May 2021), the Cochrane central register of controlled trials (Issue 2, May 2021) and conference proceedings between 2006 and 2020. Results were reported as pooled relative risks (RRs) with 95% confidence intervals (CIs) to summarise the effect of each comparison tested, with treatments ranked according to p score.

Results: We identified 15 RCTs in total for the treatment of MC. Entocort 9 mg ranked first for clinical (RR: 4.89, CI: 2.43-9.83; p score: 0.86) and histological (RR: 13.39, CI: 1.92-93.44; p score 0.94) induction of remission, whilst VSL#3 ranked second for clinical induction (RR: 5.30, CI: 0.68-41.39; p score 0.81). Budenofalk 6 mg/3 mg alternate day dosing ranked first for clinical maintenance of remission (RR: 3.68, CI: 0.08-159.92, p-score 0.65). Entocort and Budenofalk were associated with the greatest adverse events for induction and maintenance of clinical remission, respectively, although the overall withdrawal numbers for treatment versus placebo groups were 10.9% (22/201) and 10.5% (20/190), respectively.

Conclusion: Entocort 9 mg/day ranked first among the treatment options in inducing remission and Budenofalk 6 mg/3 mg alternate day dosing for maintaining remission in the treatment of MC. Moving forward, mechanistic studies exploring the differences between Entocort and Budenofalk would be valuable whilst future RCT studies are needed in non-corticosteroidal maintenance, particularly looking into immunomodulators, biologics and probiotics.

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显微结肠炎药物治疗的疗效和安全性:系统综述和网络荟萃分析。
背景:治疗显微镜下结肠炎(MC)的主要药物是布地奈德。然而,布地奈德诱导和维持缓解的最佳配方和剂量尚未得到明确证明。目的:比较诱导和维持mc缓解的治疗方法的有效性和安全性。设计:我们对随机对照试验(RCTs)进行了荟萃分析,比较了两种治疗或安慰剂在诱导和维持mc临床和组织学缓解方面的作用。我们检索了MEDLINE(1946年至2021年5月)、EMBASE和EMBASE Classis(1947年至2021年5月)、Cochrane对照试验中央注册库(第2期,2021年5月)和2006年至2020年的会议记录。结果报告为汇总相对危险度(rr), 95%置信区间(ci),以总结每个比较的效果,并根据p评分对治疗进行排序。结果:共纳入15项rct,依托可特9 mg在临床应用中排名第一(RR: 4.89, CI: 2.43-9.83;p评分:0.86)和组织学(RR: 13.39, CI: 1.92 ~ 93.44;p评分0.94)诱导缓解,而VSL#3在临床诱导方面排名第二(RR: 5.30, CI: 0.68-41.39;P值0.81)。Budenofalk 6mg / 3mg隔天给药在临床维持缓解方面排名第一(RR: 3.68, CI: 0.08 ~ 159.92, p值0.65)。Entocort和Budenofalk分别与诱导和维持临床缓解的最大不良事件相关,尽管与安慰剂组相比,治疗组的总停药数分别为10.9%(22/201)和10.5%(20/190)。结论:在诱导缓解和Budenofalk 6 mg/ 3mg隔天剂量维持缓解方面,Entocort 9mg /天在治疗方案中排名第一。下一步,探索Entocort和Budenofalk之间差异的机制研究将是有价值的,而未来的RCT研究需要在非皮质类固醇维持方面进行,特别是研究免疫调节剂、生物制剂和益生菌。
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Therapeutic Advances in Gastroenterology
Therapeutic Advances in Gastroenterology Medicine-Gastroenterology
自引率
2.40%
发文量
103
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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