Upadacitinib as monotherapy in patients with rheumatoid arthritis and prior inadequate response to methotrexate: results at 260 weeks from the SELECT-MONOTHERAPY randomised study.

IF 5.1 2区 医学 Q1 RHEUMATOLOGY
Josef S Smolen, Paul Emery, William Rigby, Yoshiya Tanaka, Juan Ignacio Vargas, Manish Jain, Koji Kato, Kyle M Carter, Nasser Khan, Charles Phillips, Sebastian Meerwein, Stanley B Cohen
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引用次数: 0

Abstract

Introduction: The phase III SELECT-MONOTHERAPY trial (NCT02706951) demonstrated the safety and efficacy of upadacitinib (UPA) monotherapy through 84 weeks in patients with rheumatoid arthritis who responded inadequately to methotrexate. Here we report week 260 results.

Methods: Patients were randomised to continue methotrexate or UPA 15 mg (UPA15) or 30 mg (UPA30) monotherapy for 14 weeks. From week 14, patients continuing methotrexate switched to UPA15 or UPA30 per prespecified assignment; patients randomised to UPA continued treatment. Following a protocol amendment, all cohorts switched to open-label UPA15. Safety was summarised using exposure-adjusted event and incidence rates. Efficacy was reported as observed and using non-responder imputation (NRI).

Results: Of 648 randomised patients, 598 entered the long-term extension. Of these, 249 (41.6%) discontinued study drug by week 260 primarily due to adverse events (14.5%), consent withdrawal (9.9%), lost to follow-up (3.3%), lack of efficacy (2.2%), COVID-19 (0.7%) or other reasons (11.0%). Rates of herpes zoster, non-melanoma skin cancer, hepatic disorder, neutropenia, lymphopenia and creatine kinase elevation were higher with UPA30 versus UPA15. Long-term UPA safety data were consistent with the established UPA safety profile. Based on NRI, >39% of patients treated continuously with UPA achieved low disease activity per Clinical Disease Activity Index ≤10 (UPA15, n=93/217; UPA30, n=91/215) and 28-joint Disease Activity Score using C reactive protein ≤3.2 (UPA15, n=90/217; UPA30, n=94/215) at week 260. Efficacy was similar among patients switching from methotrexate to UPA.

Conclusion: No new safety risks were identified with long-term UPA treatment. UPA monotherapy was efficacious in treating rheumatoid arthritis through week 260.

Trial registration number: NCT02706951.

Upadacitinib单药治疗既往对甲氨蝶呤反应不足的类风湿关节炎患者:选择单药随机研究260周的结果
III期选择性单药治疗试验(NCT02706951)通过84周的试验证明了upadacitinib (UPA)单药治疗对甲氨蝶呤反应不足的类风湿关节炎患者的安全性和有效性。这里我们报告第260周的结果。方法:患者随机分为甲氨蝶呤或UPA 15mg (UPA15)或30mg (UPA30)单药治疗14周。从第14周开始,继续使用甲氨蝶呤的患者根据预先指定的分配切换到UPA15或UPA30;随机分配到UPA组的患者继续治疗。在协议修订后,所有队列切换到开放标签UPA15。使用暴露调整后的事件和发生率来总结安全性。疗效是通过观察和使用无反应归算(NRI)来报告的。结果:648例随机患者中,598例进入长期延长期。其中,249例(41.6%)在第260周前停药,主要原因是不良事件(14.5%)、同意退出(9.9%)、失访(3.3%)、缺乏疗效(2.2%)、COVID-19(0.7%)或其他原因(11.0%)。UPA30与UPA15相比,带状疱疹、非黑色素瘤皮肤癌、肝脏疾病、中性粒细胞减少症、淋巴细胞减少症和肌酸激酶升高的发病率更高。长期UPA安全性数据与已建立的UPA安全性概况一致。基于NRI, bbbb39 %持续接受UPA治疗的患者每临床疾病活动指数≤10达到低疾病活动(UPA15, n=93/217;UPA30, n=91/215)和28关节疾病活动评分采用C反应蛋白≤3.2 (UPA15, n=90/217;UPA30, n=94/215)在第260周。从甲氨蝶呤转向UPA的患者的疗效相似。结论:长期UPA治疗未发现新的安全风险。到第260周,UPA单药治疗类风湿关节炎有效。试验注册号:NCT02706951。
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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