Effectiveness of tofacitinib in patients with ulcerative colitis: an updated systematic review and meta-analysis of real-world studies.

IF 3.3 Q2 GASTROENTEROLOGY & HEPATOLOGY BMJ Open Gastroenterology Pub Date : 2024-12-12 DOI:10.1136/bmjgast-2024-001347
Chien-Hung Lin, Wen-Sheng Liu, Chuan Wan, Hsin-Hui Wang
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Abstract

Objectives: This study aimed to evaluate the real-world effectiveness of tofacitinib for treating moderate-to-severe ulcerative colitis (UC).

Design: Systematic review and meta-analysis.

Data sources: PubMed, EMBASE and Cochrane CENTRAL databases were searched from inception up to 18 July 2023. Reference lists of included studies were manually searched to identify potentially relevant studies not found in the databases.

Eligibility criteria: Eligible studies included real-world observational studies, reported in English, on patients with moderate-to-severe UC treated with tofacitinib, defined by the Partial Mayo Score. Excluded were clinical trials, reviews, letters, conference abstracts, case reports and studies involving patients with mixed Crohn's disease.

Data extraction and synthesis: Two independent reviewers extracted data and recorded it in Excel. Quality assessment was performed using the Newcastle-Ottawa scale. Meta-analysis was performed using random-effects models due to high heterogeneity across studies.

Results: 19 studies containing a total of 2612 patients were included. Meta-analysis revealed that clinical response rates were 58% at week 8, 61% at weeks 12-16, 51% at weeks 24-26 and 51% at week 52. Clinical remission rates were 39% at week 8, 43% at weeks 12-16, 40% at weeks 24-26 and 43% at week 52. Corticosteroid-free clinical remission rates were 33% at week 8, 37% at weeks 12-16, 32% at weeks 24-26 and 40% at week 52.

Conclusion: This meta-analysis of real-world studies indicates that treatment of UC with tofacitinib is associated with favourable clinical response and remission rates in the induction and maintenance phases.

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托法替尼在溃疡性结肠炎患者中的有效性:一项对现实世界研究的最新系统综述和荟萃分析。
研究目的本研究旨在评估托法替尼治疗中重度溃疡性结肠炎(UC)的实际疗效:设计:系统综述和荟萃分析:数据来源:检索了PubMed、EMBASE和Cochrane CENTRAL数据库,检索时间从开始至2023年7月18日。人工检索了纳入研究的参考文献列表,以确定数据库中未发现的潜在相关研究:符合条件的研究包括用英语报告的真实世界观察性研究,研究对象为接受托法替尼治疗的中重度 UC 患者(以部分梅奥评分为标准)。不包括临床试验、综述、信件、会议摘要、病例报告以及涉及混合型克罗恩病患者的研究:两名独立审稿人提取数据并记录在 Excel 中。采用纽卡斯尔-渥太华量表进行质量评估。由于各研究之间存在高度异质性,因此采用随机效应模型进行了 Meta 分析:结果:共纳入 19 项研究,包含 2612 名患者。元分析显示,第 8 周的临床应答率为 58%,第 12-16 周为 61%,第 24-26 周为 51%,第 52 周为 51%。临床缓解率在第 8 周为 39%,第 12-16 周为 43%,第 24-26 周为 40%,第 52 周为 43%。不使用皮质类固醇的临床缓解率在第8周为33%,第12-16周为37%,第24-26周为32%,第52周为40%:这项真实世界研究的荟萃分析表明,使用托法替尼治疗 UC 在诱导和维持阶段具有良好的临床反应和缓解率。
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来源期刊
BMJ Open Gastroenterology
BMJ Open Gastroenterology GASTROENTEROLOGY & HEPATOLOGY-
CiteScore
5.90
自引率
3.20%
发文量
68
审稿时长
2 weeks
期刊介绍: BMJ Open Gastroenterology is an online-only, peer-reviewed, open access gastroenterology journal, dedicated to publishing high-quality medical research from all disciplines and therapeutic areas of gastroenterology. It is the open access companion journal of Gut and is co-owned by the British Society of Gastroenterology. The journal publishes all research study types, from study protocols to phase I trials to meta-analyses, including small or specialist studies. Publishing procedures are built around continuous publication, publishing research online as soon as the article is ready.
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