Division of Rheumatology, Department of Internal Medicine and Department of Medicine, Faculty of Medicine, Geneva University Hospitals, Geneve, Switzerland
Centre for Epidemiology versus Arthritis, Centre for Musculoskeletal Research, Faculty of Biology, Medicine and Health, University of Manchester, Manchester Academic Health Science Centre, Manchester, UK.
Ann Rheum Dis. 2022 Oct;81(10):1358-1366. doi: 10.1136/annrheumdis-2022-222586. Epub 2022 Jun 15.
JAK-inhibitors (JAKi), recently approved in rheumatoid arthritis (RA), have changed the landscape of treatment choices. We aimed to compare the effectiveness of four current second-line therapies of RA with different modes of action, since JAKi approval, in an international collaboration of 19 registers.
In this observational cohort study, patients initiating tumour necrosis factor inhibitors (TNFi), interleukin-6 inhibitors (IL-6i), abatacept (ABA) or JAKi were included. We compared the effectiveness of these treatments in terms of drug discontinuation and Clinical Disease Activity Index (CDAI) response rates at 1 year. Analyses were adjusted for patient, disease and treatment characteristics, including lines of therapy and accounted for competing risk.
We included 31 846 treatment courses: 17 522 TNFi, 2775 ABA, 3863 IL-6i and 7686 JAKi. Adjusted analyses of overall discontinuation were similar across all treatments. The main single reason of stopping treatment was ineffectiveness. Compared with TNFi, JAKi were less often discontinued for ineffectiveness (adjusted HR (aHR) 0.75, 95% CI 0.67 to 0.83), as was IL-6i (aHR 0.76, 95% CI 0.67 to 0.85) and more often for adverse events (aHR 1.16, 95% CI 1.03 to 1.33). Adjusted CDAI response rates at 1 year were similar between TNFi, JAKi and IL-6i and slightly lower for ABA.
The adjusted overall drug discontinuation and 1 year response rates of JAKi and IL-6i were similar to those observed with TNFi. Compared with TNFi, JAKi were more often discontinued for adverse events and less for ineffectiveness, as were IL-6i.
JAK 抑制剂(JAKi)最近在类风湿关节炎(RA)中获得批准,改变了治疗选择的格局。我们旨在比较四种不同作用机制的二线治疗 RA 的当前药物,包括 JAKi 获批后,在 19 个登记处的国际合作中。
在这项观察性队列研究中,纳入了开始使用肿瘤坏死因子抑制剂(TNFi)、白细胞介素-6 抑制剂(IL-6i)、阿巴西普(ABA)或 JAKi 的患者。我们比较了这些治疗方法在 1 年时停药和临床疾病活动指数(CDAI)应答率方面的有效性。分析调整了患者、疾病和治疗特征,包括治疗线数,并考虑了竞争风险。
我们纳入了 31846 个治疗疗程:17522 个 TNFi、2775 个 ABA、3863 个 IL-6i 和 7686 个 JAKi。所有治疗方法的总体停药调整分析结果相似。停止治疗的主要原因是无效。与 TNFi 相比,JAKi 因无效而停药的可能性较小(调整后的 HR[aHR]0.75,95%CI 0.67 至 0.83),IL-6i 也是如此(aHR 0.76,95%CI 0.67 至 0.85),而因不良反应而停药的可能性更大(aHR 1.16,95%CI 1.03 至 1.33)。1 年时的调整 CDAI 应答率在 TNFi、JAKi 和 IL-6i 之间相似,而 ABA 略低。
JAKi 和 IL-6i 的调整后整体药物停药率和 1 年应答率与 TNFi 观察到的相似。与 TNFi 相比,JAKi 因不良反应而停药的可能性更大,因无效而停药的可能性更小,IL-6i 也是如此。