Konzett Victoria, Smolen Josef S, Nash Peter, Aletaha Daniel, Winthrop Kevin, Dörner Thomas, Fleischmann Roy, Tanaka Yoshiya, Primdahl Jette, Baraliakos Xenofon, McInnes Iain B, Trauner Michael, Sattar Naveed, de Wit Maarten, Schoones Jan W, Kerschbaumer Andreas
Department of Medicine III, Division of Rheumatology, Medical University of Vienna, Vienna, Austria.
Department of Medicine III, Division of Rheumatology, Medical University of Vienna, Vienna, Austria.
Ann Rheum Dis. 2025 May;84(5):680-696. doi: 10.1016/j.ard.2025.01.023. Epub 2025 Feb 10.
This systematic literature review (SLR) on efficacy outcomes was performed to inform the 2024 update of the expert consensus statement on the treatment of immune-mediated inflammatory diseases (IMIDs) with Janus kinase inhibitors (JAKi).
An update of the 2019 SLR was performed in MEDLINE, Embase, and the Cochrane Library. For efficacy, randomised, placebo (PLC)- or active-controlled trials on all JAKi investigated in IMIDs, as well as cohort and claims data for conditions where such studies were not available, were included.
In total, 10,556 records were screened, and 182 articles were included in the final analysis, investigating 21 JAKi in 51 IMIDs. Forty-three phase 2 and 59 phase 3 trials as well as 9 strategic trials and 72 pilot or cohort studies and case series were considered. JAKi demonstrated efficacy both in PLC-controlled trials as well as in head-to-head comparisons against active comparators, with 93 of 102 randomised controlled trials (RCTs) meeting their primary endpoints. Since 2019, 8 JAKi have received approval by the Federal Drug Agency and the European Medicine Agency for treatment of 11 IMIDs; of these, for 2, no approved disease-modifying antirheumatic drug (DMARD) therapy had previously been available.
JAKi are effective for treating IMIDs, and various compounds have recently been approved. The impact of Janus kinase (JAK) selectivity for distinct JAK-STAT pathways needs further investigation, and few data are also available on sustained disease control upon tapering or withdrawal or on the optimal strategic placement of JAKi in international treatment algorithms.
进行这项关于疗效结果的系统文献综述(SLR),为2024年关于使用Janus激酶抑制剂(JAKi)治疗免疫介导的炎症性疾病(IMIDs)的专家共识声明更新提供信息。
在MEDLINE、Embase和Cochrane图书馆对2019年的SLR进行更新。对于疗效,纳入了关于IMIDs中研究的所有JAKi的随机、安慰剂(PLC)对照或活性对照试验,以及在无法获得此类研究的情况下的队列和索赔数据。
总共筛选了10556条记录,最终分析纳入了182篇文章,研究了51种IMIDs中的21种JAKi。考虑了43项2期试验、59项3期试验以及9项战略试验和72项试点或队列研究及病例系列。JAKi在PLC对照试验以及与活性对照药的头对头比较中均显示出疗效,102项随机对照试验(RCT)中有93项达到了其主要终点。自2019年以来,8种JAKi已获得美国食品药品监督管理局和欧洲药品管理局批准用于治疗11种IMIDs;其中,有2种此前没有获批的改善病情抗风湿药(DMARD)疗法。
JAKi对治疗IMIDs有效,并且最近有多种化合物获得批准。Janus激酶(JAK)对不同JAK-STAT途径的选择性影响需要进一步研究,关于逐渐减量或停药后的持续疾病控制以及JAKi在国际治疗方案中的最佳战略定位的数据也很少。