Janus 激酶抑制剂对类风湿性关节炎的疗效:系统回顾和荟萃分析

A. Cheberda, D. Belousov
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引用次数: 0

摘要

目的 评估新型选择性口服 Janus 激活激酶抑制剂托法替尼、巴利昔替尼和乌达替尼不同给药方案对类风湿性关节炎(RA)的疗效。材料和方法。 从 MEDLINE 和 Cochrane 数据库中确定了托法替尼、巴利替尼和乌达替尼治疗类风湿关节炎的随机对照试验。随机效应模型用于估计汇总的平均差(MD)和相对风险(RR)。计算美国风湿病学会 20% (ACR20)、健康评估问卷-残疾指数 (HAQ-DI)。 结果。确定了20项总体偏倚风险较低的试验。与安慰剂相比,托法替尼、巴利替尼和乌达替尼改善了ACR20(RR,2.03;95% CI,1.87至2.20)和HAQ-DI(MD,-0.31;95% CI,-0.34至-0.28)所显示的RA控制情况。 结论 托法替尼、巴利替尼和乌达替尼能显著改善对RA的控制。为了做出进一步决策,有必要在实际临床实践中对 Janus 激酶抑制剂进行比较临床试验。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Effectiveness of  Janus kinase  inhibitors in  rheumatoid  arthritis:  systematic review  and  meta-analysis
Aim.  To assess the efficacy profiles of different dosing regimens of tofacitinib, baricitinib, and upadacitinib — novel selective oral Janus activated kinase inhibitors, in rheumatoid arthritis (RA). Materials and methods.  Randomized controlled trials of tofacitinib, baricitinib and upadacitinib in RA were identified from MEDLINE, and Cochrane databases. Random- effects models were used to estimate pooled mean differences (MD) and relative risks (RRs). American College of Rheumatology 20 % (ACR20), Health Assessment Questionnaire–Disability Index (HAQ-DI) were calculated.  Results. Twenty trials with an overall low risk of bias were identified. Tofacitinib, baricitinib, and upadacitinib improved RA control as deter -mined by ACR20 (RR, 2.03; 95 % CI, 1.87 to 2.20) and HAQ-DI (MD, −0.31; 95% CI, −0.34 to −0.28) compared with placebo.  Conclusion.  Tofacitinib, baricitinib, and upadacitinib significantly improve RA control. To make further decisions, comparative clinical trials of the Janus kinase inhibitors in the real-world clinical practice are necessary.
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