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本文引用的文献

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Letter: propensity score-handle with care.信函:倾向评分——谨慎处理。
Aliment Pharmacol Ther. 2021 Jan;53(2):360-361. doi: 10.1111/apt.16179.
2
Drug survival of anti-TNF agents compared with vedolizumab as a second-line biological treatment in inflammatory bowel disease: results from nationwide Swedish registers.比较抗 TNF 药物与维得利珠单抗作为炎症性肠病二线生物治疗药物的药物生存:来自全国瑞典登记处的结果。
Aliment Pharmacol Ther. 2021 Feb;53(4):471-483. doi: 10.1111/apt.16193. Epub 2020 Dec 19.
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Comparative Safety and Effectiveness of Vedolizumab to Tumor Necrosis Factor Antagonist Therapy for Ulcerative Colitis.比较维得利珠单抗与肿瘤坏死因子拮抗剂治疗溃疡性结肠炎的安全性和有效性。
Clin Gastroenterol Hepatol. 2022 Jan;20(1):126-135. doi: 10.1016/j.cgh.2020.10.003. Epub 2020 Oct 8.
4
Treat to Target: The Role of Histologic Healing in Inflammatory Bowel Diseases: A Systematic Review and Meta-analysis.靶向治疗:组织学愈合在炎症性肠病中的作用:系统评价和荟萃分析。
Clin Gastroenterol Hepatol. 2021 Sep;19(9):1800-1813.e4. doi: 10.1016/j.cgh.2020.09.046. Epub 2020 Sep 30.
5
Comparative effectiveness of ustekinumab or vedolizumab after one year in 130 patients with anti-TNF-refractory Crohn's disease.130 例抗 TNF 治疗失败的克罗恩病患者中乌司奴单抗或维得利珠单抗治疗 1 年后的疗效比较。
Aliment Pharmacol Ther. 2020 Oct;52(8):1341-1352. doi: 10.1111/apt.16057. Epub 2020 Sep 10.
6
Comparative safety and effectiveness of vedolizumab to tumour necrosis factor antagonist therapy for Crohn's disease.比较 vedolizumab 与肿瘤坏死因子拮抗剂治疗克罗恩病的安全性和有效性。
Aliment Pharmacol Ther. 2020 Aug;52(4):669-681. doi: 10.1111/apt.15921. Epub 2020 Jul 13.
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Comparison of Long-Term Outcomes of Infliximab versus Adalimumab Treatment in Biologic-Naïve Patients with Ulcerative Colitis.比较英夫利昔单抗与阿达木单抗治疗生物初治溃疡性结肠炎患者的长期结局。
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A propensity score weighted comparison of Vedolizumab, Adalimumab, and Golimumab in patients with ulcerative colitis.一项在溃疡性结肠炎患者中比较维得利珠单抗、阿达木单抗和古利昔单抗的倾向评分加权比较。
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Adv Ther. 2020 Jul;37(7):3417-3431. doi: 10.1007/s12325-020-01366-2. Epub 2020 May 22.
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Ustekinumab is associated with superior effectiveness outcomes compared to vedolizumab in Crohn's disease patients with prior failure to anti-TNF treatment.乌司奴单抗相较于维得利珠单抗在既往抗 TNF 治疗失败的克罗恩病患者中具有更优的有效性结局。
Aliment Pharmacol Ther. 2020 Jul;52(1):123-134. doi: 10.1111/apt.15745. Epub 2020 May 22.

炎症性肠病生物药物的头对头比较:从随机对照试验到真实世界经验

Head-to-head comparison of biological drugs for inflammatory bowel disease: from randomized controlled trials to real-world experience.

作者信息

Macaluso Fabio Salvatore, Maida Marcello, Grova Mauro, Crispino Federica, Teresi Giulia, Orlando Adele, Orlando Ambrogio

机构信息

Department of Medicine, IBD Unit, "Villa Sofia-Cervello" Hospital, Palermo, Italy.

Gastroenterology and Endoscopy Unit, "S. Elia-M. Raimondi" Hospital, Caltanissetta, Italy.

出版信息

Therap Adv Gastroenterol. 2021 May 3;14:17562848211010668. doi: 10.1177/17562848211010668. eCollection 2021.

DOI:10.1177/17562848211010668
PMID:33995582
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8111554/
Abstract

During past years, the increasing knowledge of molecular mechanisms of inflammatory bowel disease (IBD) have led to the development of several targeted biological therapies. This great expansion of available medical options has prompted the need for comparative data between drugs. For years, given that most randomized controlled trials (RCTs) were performed only placebo, this demand has clashed with the absence of head-to-head trials comparing two or more treatments. The quality of evidence coming from real-world experience was low overall, so it was extremely difficult to clarify the correct positioning of the biologicals inside the therapeutic algorithms for IBD. Fortunately, times are changing: head-to-head comparative RCTs have been conducted or are ongoing, and the methodological quality of real-world studies is gradually increasing, mainly thanks to a higher rate of application of statistical methods capable of reducing the selection bias, such as the propensity score. In this evolving scenario, the increasing number of comparative RCTs is providing high-quality data for a correct drug positioning in IBD. In parallel, real-world observational studies are supporting the data coming from RCTs, and covering those comparisons not performed in the RCT setting. We believe that there is moderate evidence already available to support clinicians in the correct choice between different biologicals, and data will certainly be more robust in the near future.

摘要

在过去几年中,对炎症性肠病(IBD)分子机制的认识不断增加,催生了几种靶向生物疗法。可用医疗选择的大幅扩展促使人们需要药物之间的对比数据。多年来,由于大多数随机对照试验(RCT)仅与安慰剂进行比较,这种需求与缺乏比较两种或更多种治疗方法的头对头试验相冲突。来自真实世界经验的证据质量总体较低,因此极难阐明生物制剂在IBD治疗算法中的正确定位。幸运的是,时代在变化:头对头比较RCT已经开展或正在进行,并且真实世界研究的方法学质量正在逐渐提高,这主要得益于能够减少选择偏倚的统计方法(如倾向评分)的更高应用率。在这种不断演变的情况下,越来越多的比较RCT正在为IBD中药物的正确定位提供高质量数据。与此同时,真实世界观察性研究正在支持来自RCT的数据,并涵盖那些在RCT环境中未进行的比较。我们认为,已经有适度的证据可支持临床医生在不同生物制剂之间做出正确选择,并且在不久的将来数据肯定会更加可靠。