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比较维得利珠单抗与其他先进疗法的疗效和安全性,评估溃疡性结肠炎治疗的净临床获益:一项网络荟萃分析。

Integrating efficacy and safety of vedolizumab compared with other advanced therapies to assess net clinical benefit of ulcerative colitis treatments: a network meta-analysis.

机构信息

Western University Schulich School of Medicine and Dentistry, London, ON, Canada.

Precision HEOR, Vancouver, BC, Canada.

出版信息

Expert Rev Gastroenterol Hepatol. 2021 Jun;15(6):711-722. doi: 10.1080/17474124.2021.1880319. Epub 2021 Mar 4.

DOI:10.1080/17474124.2021.1880319
PMID:33599181
Abstract

: Because only one head-to-head randomized trial of biologics for moderate-to-severe UC has been performed, indirect treatment comparisons remain important. This systematic review and network meta-analysis examined efficacy and safety of biologics and tofacitinib for moderate-to-severe UC, using vedolizumab as reference.: Relevant studies (N = 19) of vedolizumab, adalimumab, infliximab, golimumab, ustekinumab, and tofacitinib were identified. Study design differences were addressed by assessing efficacy outcomes conditional on response at maintenance initiation. Primary analysis used fixed-effect models to estimate odds ratios for efficacy and safety endpoints.: Compared with vedolizumab 300 mg, adalimumab 160/80 mg was associated with less clinical remission (odds ratio, 0.69 [95% credible interval, 0.54-0.88]), and infliximab 5 mg/kg was associated with more clinical remission (1.67 [1.16-2.42]) and response (1.63 [1.15-2.30]). Adalimumab 40 mg, golimumab 50 mg, and ustekinumab 90 mg Q12W had significantly lower clinical remission rates during maintenance (0.62 [0.45-0.86], 0.55 [0.32-0.95], and 0.59 [0.35-0.99]) versus vedolizumab 300 mg Q8W. Response results were similar. Tofacitinib 10 mg had the highest maintenance treatment efficacy estimates and highest infection risk.: Network meta-analysis and novel integrated benefit-risk analysis suggest a potentially favorable efficacy-safety balance for vedolizumab vs adalimumab and other advanced UC therapies.

摘要

: 由于仅开展了一项生物制剂治疗中重度 UC 的头对头随机试验,间接治疗比较仍然很重要。本系统评价和网络荟萃分析使用维得利珠单抗作为参照,评估了生物制剂和托法替尼治疗中重度 UC 的疗效和安全性。: 共纳入了 19 项关于维得利珠单抗、阿达木单抗、英夫利昔单抗、戈利木单抗、乌司奴单抗和托法替尼的研究。通过评估维持治疗起始时应答者的疗效结局,解决了研究设计差异。主要分析采用固定效应模型估计疗效和安全性结局的优势比。: 与维得利珠单抗 300 mg 相比,阿达木单抗 160/80 mg 与较低的临床缓解相关(优势比,0.69 [95%可信区间,0.54-0.88]),英夫利昔单抗 5 mg/kg 与更高的临床缓解(1.67 [1.16-2.42])和应答(1.63 [1.15-2.30])相关。阿达木单抗 40 mg、戈利木单抗 50 mg 和乌司奴单抗 90 mg Q12W 维持治疗时的临床缓解率显著较低(0.62 [0.45-0.86]、0.55 [0.32-0.95] 和 0.59 [0.35-0.99]),而维得利珠单抗 300 mg Q8W 则更高。应答结果相似。托法替尼 10 mg 的维持治疗疗效估计值最高,感染风险最高。: 网络荟萃分析和新颖的综合获益-风险分析表明,维得利珠单抗与阿达木单抗和其他先进的 UC 治疗相比,具有潜在有利的疗效-安全性平衡。

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