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Efficacy of biologic therapies for biologic-naïve Japanese patients with moderately to severely active ulcerative colitis: a network meta-analysis

机译:生物疗法对生物学治疗的疗效,日本患者适度至严重活性溃疡性结肠炎:网络元分析

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摘要

Background/Aims Several biologic therapies are approved in Japan to treat moderately to severely active ulcerative colitis (UC), but there are no published comparative efficacy studies in a Japanese population. We compared the efficacy of biologics approved in Japan (adalimumab, infliximab, golimumab, and vedolizumab) for treating biologic-naïve patients with UC at their approved doses. Methods A targeted literature review identified 4 randomized controlled trials of biologics for UC in biologic-naïve Japanese patients. For each study, efficacy outcome data from induction (weeks 6–12) and maintenance (weeks 30–60) treatment were extracted for analysis. Treatment effects on clinical response, clinical remission, and mucosal healing relative to the average placebo results across all trials were estimated using network meta-analyses followed by transformation into probabilities and odds ratios (OR). Results At the end of induction, the likelihood of clinical response and clinical remission was highest with infliximab (OR: 2.12 and 2.35, respectively) and vedolizumab (OR: 2.10 and 2.32, respectively); the likelihood of mucosal healing was highest with infliximab (OR: 2.24) and adalimumab (OR: 1.86). During maintenance, the likelihood of clinical response and clinical remission was highest with vedolizumab (OR: 6.44 and 4.68, respectively) and golimumab (OR: 5.13 and 3.84, respectively); the likelihood of mucosal healing was significantly higher than placebo with all biologics. Conclusions All active treatments were efficacious compared with placebo. Infliximab and vedolizumab had the highest odds for induction of clinical response, remission, and mucosal healing. Golimumab and vedolizumab had numerically higher odds of achieving efficacy outcomes in the maintenance phase.
机译:背景/目的几种生物疗法被批准在日本治疗中度至重度活动性溃疡性结肠炎(UC),但在日本的人口都没有发表的比较有效性研究。我们比较了在其批准的剂量治疗的生物初治患者与UC批准在日本(阿达木单抗,英利昔单抗,戈利木单抗和维多珠单抗),生物制剂的疗效。方法有针对性的文献综述中的生物,天真日本患者鉴定4个随机对照生物制剂的试验的UC。对于每个研究中,从诱导(周6-12)和维护疗效结果数据(周30-60)处理中提取用于分析。使用网络荟萃分析随后转化成概率和的比值比(OR)临床反应,临床缓解,并且在所有试验中的平均结果安慰剂愈合相对粘膜治疗效果估计。结果在诱导结束时,临床反应和临床缓解的可能性最高与英夫利昔单抗(OR:2.12和2.35,分别地)和维多珠单抗(OR:2.10和2.32,分别地);粘膜愈合的可能性最高,英利昔单抗(OR:2.24)和阿达木单抗(OR:1.86)。在维护期间,临床反应和临床缓解的可能性最高与维多珠单抗(OR:6.44和4.68,分别地)和戈利木单抗(OR:5.13和3.84,分别地);粘膜愈合的可能性比所有的生物制剂安慰剂显著较高。与安慰剂组相比结论所有积极治疗是有效的。英夫利昔单抗和维多珠单抗具有最高的赔率为临床反应,缓解和粘膜愈合的诱导。戈利木单抗和维多珠单抗曾在维护阶段取得疗效结果的数值较高的赔率。

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