Comparative maintenance performance of all biologic agents and small molecules in ulcerative colitis: a network meta-analysis.

IF 4.6 Q2 MATERIALS SCIENCE, BIOMATERIALS ACS Applied Bio Materials Pub Date : 2024-05-01 Epub Date: 2024-03-12 DOI:10.1097/MEG.0000000000002751
Theodore Rokkas, Javier P Gisbert, Konstantinos Ekmektzoglou, Themistocles Dassopoulos, Yaron Niv, Colm O'Morain
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Abstract

Background and aims: Βiologic agents and small molecules have expanded the therapeutic armamentarium of moderate to severe ulcerative colitis (UC). However, their comparative efficacy and safety performance as maintenance treatments have not been sufficiently explored. We performed a systematic review and network meta-analysis (NWM) to assess the comparative efficacy and safety of all approved and emerging treatments for maintenance in moderate to severe UC.

Methods: We searched Pubmed/Medline, EMBASE, and Cochrane Library databases for relevant RCTs through April 2023. The primary endpoint was clinical remission at the end of the maintenance therapy. Data were analyzed by means of a Bayesian NWM. The ranking probability concerning efficacy and safety was evaluated by means of surfaces under cumulative ranking (SUCRA) values.

Results: There were 20 eligible RCTs with 7660 patients randomized to 20 treatments. RCTs were grouped into two study designs, that is, re-randomization of patients after an induction period and treat-through patients. Concerning efficacy, in re-randomized patients, upadacitinib 30 mg/day was ranked first (SUCRA 94.9%) whereas in treat-through patients etrasimod 2 mg/day was ranked first (SUCRA 91.1%). The integrated efficacy-safety hierarchical analysis, showed that tofacitinib 10 mg had the best efficacy-safety therapeutic profile in re-randomized patients, whereas in treat-through patients infliximab 3.5 mg/Kg Q8W showed the best efficacy-safety profile.

Conclusion: For maintenance treatment, in moderate to severe UC, this NWM showed that upadacitinib 30 mg/day and etrasimod 2 mg/day were ranked best for efficacy in re-randomized and treat-through patients respectively. Tofacitinib 10 mg/day and infliximab 3.5 mg/Kg Q8W showed the best efficacy-safety therapeutic profile in re-randomized and treat-through patients respectively.

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所有生物制剂和小分子药物在溃疡性结肠炎中的维持效果比较:网络荟萃分析。
背景和目的:生物制剂和小分子药物扩大了中重度溃疡性结肠炎(UC)的治疗范围。然而,它们作为维持治疗药物的疗效和安全性比较尚未得到充分探讨。我们进行了一项系统性综述和网络荟萃分析(NWM),以评估所有已获批准和新出现的中重度 UC 维持治疗药物的疗效和安全性比较:我们检索了 Pubmed/Medline、EMBASE 和 Cochrane Library 数据库中截至 2023 年 4 月的相关 RCT。主要终点是维持治疗结束时的临床缓解。数据采用贝叶斯NWM方法进行分析。有关疗效和安全性的排序概率通过累积排序(SUCRA)值表面进行评估:共有 20 项符合条件的 RCT,7660 名患者随机接受了 20 种治疗。临床试验分为两种研究设计,即诱导期后重新随机化患者和直通治疗患者。关于疗效,在重新随机化的患者中,达帕替尼 30 毫克/天的疗效排名第一(SUCRA 94.9%),而在直通治疗的患者中,依曲莫德 2 毫克/天的疗效排名第一(SUCRA 91.1%)。疗效-安全性综合分层分析显示,在重新随机化的患者中,托法替尼10毫克的疗效-安全性治疗概况最好,而在直通治疗的患者中,英夫利西单抗3.5毫克/千克Q8W的疗效-安全性概况最好:对于中度至重度 UC 的维持治疗,这项新药研究显示,在重新随机化患者和通过治疗的患者中,乌达帕替尼 30 毫克/天和依曲莫德 2 毫克/天的疗效分别名列前茅。托法替尼 10 毫克/天和英夫利昔单抗 3.5 毫克/千克 Q8W 分别在重新随机化和通过治疗的患者中显示出最佳疗效和安全性。
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
ACS Applied Bio Materials
ACS Applied Bio Materials Chemistry-Chemistry (all)
CiteScore
9.40
自引率
2.10%
发文量
464
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