Therapeutic approaches for difficult-to-treat rheumatoid arthritis: a systematic literature review of current evidence.

IF 5.3 2区 医学 Q1 RHEUMATOLOGY
Golnaz Shams, András Miklós Dorgó, Chiara Ripepi, Emma Wettersand, Ewa Malczuk, Caroline Neumeister, Slađana Rumpl Tunjić, Brigitte Wildner, Hendrik Schulze-Koops, György Nagy, João Eurico Fonseca, Jacob M van Laar, Paco M J Welsing, Paul Studenic
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引用次数: 0

Abstract

Objective: This systematic literature review (SLR) aims to update the evidence regarding therapeutic strategies in difficult-to-treat rheumatoid arthritis (D2T RA), building on the previous SLR informing the European Alliance of Associations for Rheumatology (EULAR) points to consider for the management of D2T RA.

Methods: Three research questions addressed efficacy or safety of treatments in patients with RA with (1) active disease and limited treatment options; (2) active disease with ≥2 prior biologic/targeted synthetic disease-modifying antirheumatic drugs (b/tsDMARDs) and (3) poor health-related quality of life and low objective disease activity (non-pharmacological interventions). MEDLINE, Embase and Cochrane Library were searched until July 2025. Meta-analysis and meta-regression were conducted.

Results: We screened 8589 records and included 131 studies. For research question (RQ)1, evidence on DMARD efficacy and safety was synthesised across a wide spectrum of comorbidities including obesity, cardiovascular disease, history of malignancy and respiratory comorbidities. For RQ2, all b/tsDMARDs except otilimab demonstrated better efficacy than placebo (mostly high risk of bias). Meta-regression showed efficacy was maintained for Janus kinase inhibitors (JAKi) despite increasing number of prior bDMARD failures (1 to ≥3). Safety results confirmed the increased occurrence of infection and malignancy with JAKi. For RQ3, limited evidence suggested orthopaedic surgical intervention as a potential non-pharmacological option in patients with D2T RA.

Conclusions: This SLR summarised evidence supporting DMARD efficacy/safety across multiple comorbidities. In patients with active RA with ≥2 prior bDMARDs, JAKi offer substantial clinical benefits but require careful risk stratification given cardiovascular and malignancy risks. Furthermore, standardised reporting and dedicated studies on non-pharmacological interventions are urgently needed.

Prospero registration number: CRD42024593584.

难治性类风湿关节炎的治疗方法:当前证据的系统文献综述。
目的:本系统文献综述(SLR)旨在更新关于难治性类风湿关节炎(D2T RA)治疗策略的证据,在先前SLR的基础上,告知欧洲风湿病协会联盟(EULAR)关于D2T RA治疗的考虑点。方法:三个研究问题涉及治疗的有效性或安全性(1)活动性疾病和有限的治疗方案;(2)活动性疾病,既往使用≥2种生物/靶向合成抗风湿药物(b/tsDMARDs);(3)健康相关生活质量差,客观疾病活动性低(非药物干预)。MEDLINE, Embase和Cochrane图书馆被检索到2025年7月。进行meta分析和meta回归。结果:我们筛选了8589条记录,包括131项研究。对于研究问题(RQ)1,综合了DMARD有效性和安全性的证据,包括肥胖、心血管疾病、恶性肿瘤史和呼吸系统合并症等广泛的合并症。对于RQ2,除奥替单抗外,所有b/ tsdmard均表现出优于安慰剂的疗效(主要是高偏倚风险)。meta回归显示,尽管先前bDMARD失败的数量增加(1至≥3),但Janus激酶抑制剂(JAKi)的疗效仍保持不变。安全性结果证实JAKi感染和恶性肿瘤发生率增加。对于RQ3,有限的证据表明骨科手术干预是D2T类风湿性关节炎患者的潜在非药物选择。结论:该SLR总结了支持DMARD在多种合并症中的有效性/安全性的证据。对于既往bdmard≥2例的活动性RA患者,JAKi提供了实质性的临床益处,但考虑到心血管和恶性肿瘤风险,需要仔细的风险分层。此外,迫切需要对非药物干预措施进行标准化报告和专门研究。普洛斯彼罗注册号:CRD42024593584。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
RMD Open
RMD Open RHEUMATOLOGY-
CiteScore
7.30
自引率
6.50%
发文量
205
审稿时长
14 weeks
期刊介绍: RMD Open publishes high quality peer-reviewed original research covering the full spectrum of musculoskeletal disorders, rheumatism and connective tissue diseases, including osteoporosis, spine and rehabilitation. Clinical and epidemiological research, basic and translational medicine, interesting clinical cases, and smaller studies that add to the literature are all considered.
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