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系统性评价和荟萃分析,为日本风湿病学会类风湿关节炎管理临床实践指南 2024 年更新版

Systematic review and meta-analysis for the 2024 update of the Japan College of Rheumatology clinical practice guidelines for the management of rheumatoid arthritis.

机构信息

Department of Rheumatology and Clinical Immunology, Graduate School of Medicine, Kyoto University, Kyoto, Japan.

Department of Pharmacology, National Defense Medical College, Tokorozawa, Japan.

出版信息

Mod Rheumatol. 2024 Oct 15;34(6):1079-1094. doi: 10.1093/mr/roae049.

Abstract

OBJECTIVES

The aim of this article is to update evidence on the efficacy and safety of disease-modifying antirheumatic drugs (DMARDs) and provide information to the taskforce for the 2024 update of the Japan College of Rheumatology clinical practice guidelines for the management of rheumatoid arthritis (RA).

METHODS

We searched various databases for randomised controlled trials on RA published until June 2022, with no language restriction. For each of the 15 clinical questions, two independent reviewers screened the articles, evaluated the core outcomes, and performed meta-analyses.

RESULTS

Subcutaneous injection of methotrexate (MTX) showed similar efficacy to oral MTX in MTX-naïve RA patients. Ozoralizumab combined with MTX improved drug efficacy compared to the placebo in RA patients with inadequate response (IR) to conventional synthetic DMARD (csDMARD). Rituximab with and without concomitant csDMARDs showed similar efficacy to other biological DMARDs (bDMARDs) in bDMARD-IR RA patients. Combined Janus kinase inhibitors and MTX achieved similar clinical responses and equal safety during a 4-year period compared to tumour necrosis factor inhibitors in MTX-IR RA patients. Biosimilars showed efficacy equivalent to that of the original bDMARDs in csDMARD-IR and bDMARD-IR RA patients.

CONCLUSIONS

This systematic review provides latest evidence for the 2024 update of the Japan College of Rheumatology clinical practice guidelines for RA management.

摘要

目的

本文旨在更新疾病修饰抗风湿药物(DMARDs)的疗效和安全性证据,并为 2024 年日本风湿病学会临床实践指南更新提供信息,以管理类风湿关节炎(RA)。

方法

我们在没有语言限制的情况下,对截至 2022 年 6 月发表的 RA 随机对照试验进行了各种数据库搜索。对于每个 15 个临床问题,两位独立评审员筛选了文章,评估了核心结局,并进行了荟萃分析。

结果

在 MTX 初治 RA 患者中,皮下注射甲氨蝶呤(MTX)与口服 MTX 疗效相似。奥扎鲁单抗联合 MTX 改善了对常规合成 DMARD(csDMARD)应答不足的 RA 患者的药物疗效。利妥昔单抗联合和不联合 csDMARDs 在 bDMARD-IR RA 患者中与其他生物 DMARDs(bDMARDs)疗效相似。联合 Janus 激酶抑制剂和 MTX 在 MTX-IR RA 患者中与肿瘤坏死因子抑制剂相比,在 4 年期间取得了相似的临床反应和相同的安全性。生物类似药在 csDMARD-IR 和 bDMARD-IR RA 患者中显示出与原始 bDMARDs 等效的疗效。

结论

本系统评价为 2024 年日本风湿病学会 RA 管理临床实践指南更新提供了最新证据。

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