Unit for Clinical Therapy Research, Inflammatory Diseases (ClinTRID) , Karolinska Institute , Stockholm , Sweden.
Rheumatology, Department of Clinical Sciences , Malmö, Lund University , Malmö , Sweden.
RMD Open. 2016 Jan 14;2(1):e000133. doi: 10.1136/rmdopen-2015-000133. eCollection 2016.
Treatment with tumour necrosis factor (TNF) blockers, once started as therapy for rheumatoid arthritis (RA), is usually continued indefinitely. The aim of this trial was to assess the possibility of discontinuing treatment with adalimumab (ADA) while maintaining remission in patients with RA with established disease in stable remission on combination therapy with ADA and methotrexate (MTX).
In a randomised, controlled, open-label pilot study of patients with RA in stable remission treated with ADA+MTX, patients were randomised in a 1:1 ratio to continue with ADA plus MTX (arm AM) or MTX monotherapy (arm M) for 52 weeks. Flare was defined as Disease Activity Score (DAS28) ≥2.6 or a change in DAS28 (ΔDAS28) of >1.2 from baseline at any time. Patients in arm M with a flare restarted ADA. The primary end point was the proportion of patients in remission at week 28.
31 patients were enrolled in the study and randomised to arm AM (n=16) or arm M (n=15). At 28 weeks, 15/16 patients (94%) and 5/15 patients (33%) in arms AM and M, respectively, were in remission (p=0.001). During the first 28 weeks, 50% (8/16) in the AM arm and 80% (12/15) in the M arm had a flare (p=0.08). The number of patients in the AM and M arms with ≥1 ΔDAS28 >1.2 during the first 28 weeks was 1/16 (6%) and 8/15 (53%), respectively (p=0.005).
In this study, remission was rarely maintained in patients with long-standing disease who discontinued ADA. Discontinuation may be feasible in only a minority of patients with established RA in stable clinical remission.
NCT00808509.
肿瘤坏死因子(TNF)阻滞剂一旦开始用于治疗类风湿关节炎(RA),通常会无限期持续使用。本试验旨在评估在阿达木单抗(ADA)联合甲氨蝶呤(MTX)治疗稳定缓解的 RA 患者中,停止 ADA 治疗而维持缓解的可能性,这些患者的疾病已经处于稳定缓解期。
在 ADA+MTX 稳定缓解的 RA 患者的随机、对照、开放性试验中,患者按 1:1 比例随机分为继续 ADA+MTX(组 AM)或 MTX 单药治疗(组 M),治疗 52 周。疾病活动度评分(DAS28)≥2.6 或与基线相比 DAS28 变化(ΔDAS28)>1.2 定义为病情加重。病情加重的组 M 患者重新开始 ADA 治疗。主要终点为第 28 周时缓解的患者比例。
31 例患者入组并随机分为 AM 组(n=16)或 M 组(n=15)。28 周时,AM 组和 M 组分别有 15/16(94%)和 5/15(33%)患者缓解(p=0.001)。在最初的 28 周内,AM 组有 50%(8/16)患者和 M 组有 80%(12/15)患者出现病情加重(p=0.08)。在最初的 28 周内,AM 组和 M 组有≥1 次 ΔDAS28>1.2 的患者分别为 1/16(6%)和 8/15(53%)(p=0.005)。
在这项研究中,长期疾病患者停止 ADA 治疗后很少能维持缓解。只有少数病情稳定缓解的 RA 患者可能能够停止 ADA 治疗。
NCT00808509。