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当前治疗早期类风湿关节炎的疗效和安全性比较:系统文献回顾和网络荟萃分析。

Comparative efficacy and safety of current therapies for early rheumatoid arthritis: a systematic literature review and network meta-analysis.

机构信息

Bristol-Myers Squibb, Princeton, NJ, USA.

Doctor Evidence LLC, Santa Monica, CA, USA, and Evidinno Outcomes Research Inc., Vancouver, BC, Canada.

出版信息

Clin Exp Rheumatol. 2020 Sep-Oct;38(5):1008-1015. Epub 2020 Apr 17.

Abstract

OBJECTIVES

This systematic literature review (SLR) and network meta-analysis (NMA) was aimed at comparing the relative efficacy and safety of abatacept (ABA) with other currently recommended therapies for patients with early RA.

METHODS

An SLR (January 1998 to June 2018) was conducted including MEDLINE®, Embase, and CENTRAL databases, and grey literature. Population was adults with active RA for ≤2 years treated with biologic DMARDs as monotherapy or in combination with conventional DMARDs. A Bayesian NMA was performed using randomised controlled trials (RCTs) and comparisons for ACR50, DAS28 remission, withdrawal due to adverse events and total withdrawal where reported.

RESULTS

Ninety publications pertaining to 69 studies (43 RCTs and 26 observational studies) were identified. Twenty-eight RCTs were eligible to be included in the NMA. ABA as monotherapy was similar to the combination of ABA+methotrexate (MTX) for ACR50 (RR: 0.82 [95% CI 0.51-1.35]), and DAS28 remission (RR: 0.69 [95% CI 0.37-1.3]), as well as for withdrawal due to AEs (RR: 2.35 [95% CI 0.69-7.38]) and all-cause withdrawal (RR: 1.73 [95% CI 0.905-3.35]). ABA as monotherapy and ABA+MTX were both comparable to all other therapies for the main efficacy and safety outcomes. Observational study data reported was congruous with the RCT analysis.

CONCLUSIONS

The results of this NMA show similar efficacy and safety between ABA (as monotherapy or in combination with MTX) and other biologics in early RA. Further comparison of different treatment options for early RA is warranted as growing research provides evidence for the application of new novel therapies for RA.

摘要

目的

本系统文献回顾(SLR)和网络荟萃分析(NMA)旨在比较阿巴西普(ABA)与其他目前推荐用于早期类风湿关节炎(RA)患者的治疗方法的相对疗效和安全性。

方法

进行了 SLR(1998 年 1 月至 2018 年 6 月),包括 MEDLINE®、Embase 和 CENTRAL 数据库以及灰色文献。人群为患有活动期 RA 不超过 2 年的成年人,接受生物 DMARD 单药或联合传统 DMARD 治疗。使用随机对照试验(RCT)和报告的 ACR50、DAS28 缓解、因不良反应停药和总停药率进行贝叶斯 NMA。

结果

共确定了 90 篇与 69 项研究(43 项 RCT 和 26 项观察性研究)相关的出版物。28 项 RCT 符合纳入 NMA 的条件。ABA 单药治疗与 ABA+甲氨蝶呤(MTX)联合治疗在 ACR50(RR:0.82[95%CI 0.51-1.35])和 DAS28 缓解(RR:0.69[95%CI 0.37-1.3])方面相似,以及因 AEs 停药(RR:2.35[95%CI 0.69-7.38])和全因停药(RR:1.73[95%CI 0.905-3.35])。ABA 单药和 ABA+MTX 与其他治疗方法在主要疗效和安全性结局方面均相当。观察性研究数据与 RCT 分析一致。

结论

本 NMA 的结果表明,早期 RA 中 ABA(单药或与 MTX 联合)与其他生物制剂的疗效和安全性相似。需要进一步比较早期 RA 的不同治疗选择,因为越来越多的研究为 RA 新疗法的应用提供了证据。

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