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生物制剂和小分子药物治疗早期类风湿关节炎疗效的贝叶斯混合治疗比较。

A Bayesian mixed treatment comparison of efficacy of biologics and small molecules in early rheumatoid arthritis.

机构信息

Rheumatology Unit, Department of Emergency and Organ Transplantations, Policlinico, Piazza G. Cesare 11, 70124, Bari, Italy.

出版信息

Clin Rheumatol. 2019 May;38(5):1309-1317. doi: 10.1007/s10067-018-04406-z. Epub 2019 Jan 10.

Abstract

The current paradigm in the management of rheumatoid arthritis (RA) is to treat patients in the early stage of the disease (ERA). Previous meta-analysis-based mixed treatment comparisons (MTCs), aimed to identify the most effective drugs in ERA, are biased by the wide "window" of early definition, ranging from 6 months to 2 years. The aim of this study was to estimate through a Bayesian Network Meta-Analysis which biologics or small molecules are more likely to achieve a 1-year good clinical response in ERA patients with disease duration < 1 year. According to the Preferred Reporting Items for Systematic Reviews and Meta-analyses statement, randomized controlled trials (RCTs) of biologic agents and small molecules in combination with MTX to treat patients affected with ERA lasting < 1 year were searched through MEDLINE, EMBASE, Cochrane Library, and Clinicaltrials.gov between 1990 and September 2017. The outcome of interest was the achievement of American College of Rheumatology (ACR) 50 and ACR 70 response at 1 year. WinBUGS 1.4 software (MRC Biostatistics Unit, Cambridge, UK) was used to perform the analyses, using a fixed effect model. Fourteen studies were included in the analysis. Tofacitinib (64.83%) followed by Etanercept (23.26%) were the drugs with the highest probability of achieving ACR50 response. Rituximab showed the highest probability of inducing ACR70 response (52.81%) followed by Etanercept (26.85%). This is the first MTC involving only RCTs on ERA patients with disease duration < 1 year. Tofacitinib and rituximab were the drugs ranked first in inducing 1-year ACR50 and ACR70 response, respectively.

摘要

当前类风湿关节炎(RA)管理的范式是在疾病早期(ERA)治疗患者。以前基于荟萃分析的混合治疗比较(MTC)旨在确定 ERA 中最有效的药物,但由于早期定义的广泛“窗口”,从 6 个月到 2 年不等,存在偏倚。本研究旨在通过贝叶斯网络荟萃分析来估计,在疾病持续时间<1 年的 ERA 患者中,哪种生物制剂或小分子更有可能在 1 年内获得良好的临床反应。根据系统评价和荟萃分析的首选报告项目声明,通过 MEDLINE、EMBASE、Cochrane 图书馆和 Clinicaltrials.gov 搜索了 1990 年至 2017 年 9 月期间生物制剂和小分子联合 MTX 治疗持续时间<1 年的 ERA 患者的随机对照试验(RCT)。感兴趣的结局是在 1 年内达到美国风湿病学会(ACR)50 和 ACR 70 反应。使用固定效应模型,使用 MRC 生物统计学单元(英国剑桥)的 WinBUGS 1.4 软件来执行分析。有 14 项研究纳入了分析。托法替尼(64.83%)紧随其后的是依那西普(23.26%)是最有可能达到 ACR50 反应的药物。利妥昔单抗显示出最高的诱导 ACR70 反应的可能性(52.81%),其次是依那西普(26.85%)。这是第一项仅涉及持续时间<1 年的 ERA 患者的 RCT 的 MTC。托法替尼和利妥昔单抗分别是诱导 1 年 ACR50 和 ACR70 反应排名第一的药物。

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