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Efficacy of synthetic and biological DMARDs: a systematic literature review informing the 2022 update of the EULAR recommendations for the management of rheumatoid arthritis

医学 托法替尼 阿巴塔克普 托珠单抗 依那西普 英夫利昔单抗 阿达木单抗 妥珠单抗 内科学 类风湿性关节炎 美罗华 来氟米特 系统回顾 阿纳基纳 梅德林 疾病 淋巴瘤 政治学 法学
作者
Andreas Kerschbaumer,Alexandre Sepriano,Sytske Anne Bergstra,Josef S Smolen,Désirée van der Heijde,Roberto Caporali,Christopher J Edwards,Patrick Verschueren,Savia de Souza,Janet Pope,Tsutomu Takeuchi,Kimme L Hyrich,Kevin Winthrop,Daniel Aletaha,Tanja Stamm,Jan W. Schoones,Robert Landewé
出处
期刊:Annals of the Rheumatic Diseases [BMJ]
卷期号:82 (1): 95-106 被引量:168
标识
DOI:10.1136/ard-2022-223365
摘要

OBJECTIVES: 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). METHODS: 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. RESULTS: 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. CONCLUSION: 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.
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