Kerschbaumer Andreas, Sepriano Alexandre, Bergstra Sytske Anne, Smolen Josef S, van der Heijde Désirée, Caporali Roberto, Edwards Christopher John, Verschueren Patrick, de Souza Savia, Pope Janet E, Takeuchi Tsutomu, Hyrich Kimme L, Winthrop Kevin L, Aletaha Daniel, Stamm Tanja A, Schoones Jan W, Landewé Robert B M
Department of Medicine III, Division of Rheumatology, Medical University of Vienna, Vienna, Austria
CHRC Campus Nova Medical School, Universidade Nova de Lisboa, Lisboa, Portugal.
Ann Rheum Dis. 2023 Jan;82(1):95-106. doi: 10.1136/ard-2022-223365. Epub 2022 Nov 11.
To update the evidence on efficacy of DMARDs (disease-modifying antirheumatic drugs) and inform the taskforce of the 2022 update of the European Alliance of Associations for Rheumatology (EULAR) recommendations for management of rheumatoid arthritis (RA).
This systematic literature review (SLR) investigated the efficacy of conventional synthetic (cs), biological (b), biosimilar and targeted synthetic (ts)DMARDs in patients with RA. Medline, EMBASE, Cochrane CENTRAL and Web of Science were used to identify all relevant articles published since the previous update in 2019 to 14 January 2022.
Of 8969 search results, 169 articles were selected for detailed review and 47 were finally included. Trials investigated the efficacy of csDMARDs, bDMARDs and tsDMARDs, DMARD switching, tapering and trials investigating different treatment strategies. The compounds investigated were csDMARDs (methotrexate (MTX), leflunomide, sulfasalazine, hydroxychloroquine), bDMARDs (abatacept, adalimumab, certolizumab-pegol, denosumab, etanercept, infliximab, levilimab, olokizumab, opineracept, rituximab, sarilumab, tocilizumab) and tsDMARDs (baricitinib, filgotinib, tofacitinib, upadacitinib). The efficacy of csDMARDs+ short-term glucocorticoids in early RA was confirmed and similar to bDMARD+MTX combination therapy. Interleukin-6 pathway inhibition was effective in trials on olokizumab and levilimab. Janus kinase inhibitor (JAKi) was efficacious in different patient populations. After insufficient response to JAKi, patients could respond to TNFi treatment. Tapering of DMARDs was feasible for a proportion of patients, who were able to taper therapy while remaining in low disease activity or remission.
The results of this SLR, together with one SLR on safety of DMARD and one on glucocorticoids, informed the taskforce of the 2022 update of the EULAR recommendations for pharmacological management of RA.
更新改善病情抗风湿药(DMARDs)疗效的证据,并为欧洲风湿病协会联盟(EULAR)2022年类风湿关节炎(RA)管理建议更新工作组提供信息。
本系统文献综述(SLR)研究了传统合成(cs)、生物(b)、生物类似物和靶向合成(ts)DMARDs在RA患者中的疗效。使用Medline、EMBASE、Cochrane CENTRAL和科学网检索2019年上次更新至2022年1月14日发表的所有相关文章。
在8969条检索结果中,169篇文章被选进行详细综述,最终纳入47篇。试验研究了csDMARDs、bDMARDs和tsDMARDs的疗效、DMARD转换、减量以及不同治疗策略的试验。所研究的化合物包括csDMARDs(甲氨蝶呤(MTX)、来氟米特、柳氮磺吡啶、羟氯喹)、bDMARDs(阿巴西普、阿达木单抗、赛妥珠单抗聚乙二醇、地诺单抗、依那西普、英夫利昔单抗、利维单抗、奥洛珠单抗、奥皮纳单抗、利妥昔单抗、托珠单抗)和tsDMARDs(巴瑞替尼、非戈替尼、托法替布、乌帕替尼)。csDMARDs联合短期糖皮质激素在早期RA中的疗效得到证实,且与bDMARD联合MTX的联合治疗相似。白细胞介素-6通路抑制在奥洛珠单抗和利维单抗试验中有效。Janus激酶抑制剂(JAKi)在不同患者群体中均有效。对JAKi反应不足的患者对肿瘤坏死因子抑制剂(TNFi)治疗有反应。部分患者可行DMARDs减量,这些患者能够在保持低疾病活动度或缓解的同时逐渐减少治疗。
本SLR的结果,连同一项关于DMARD安全性和一项关于糖皮质激素的SLR结果,为EULAR 2022年RA药物治疗管理建议更新工作组提供了信息。