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Maintenance treatment using abatacept with dose reduction after achievement of low disease activity in patients with rheumatoid arthritis (MATADOR) - A prospective, multicenter, single arm pilot clinical trial

机译:在类风湿性关节炎患者(Matador)的患者中,使用AbataCept进行剂量降低的维持治疗 - 一种预期,多中心,单臂试验临床试验

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Objectives: To preliminarily evaluate the feasibility of maintenance therapy with reduced dose of intravenous abatacept (ABT) to 250mg/body/month after achieving remission or low disease activity (LDA).Patients and methods: RA patients treated with ABT at 13 sites were enrolled in this prospective interventional pilot study during the period between March 2013 and March 2015. Inclusion criteria were (1) age at 20 years or older, (2) under treatment with monthly intravenous ABT at approved doses, (3) DAS28-CRP lower than 2.7 at least for 6 months, (4) agreed to join this trial with written informed consent and (5) body weight under 125kg. Enrolled patients were maintained with intravenous monthly ABT at a reduced dose of 250mg/body (MATADOR protocol). The primary end point was the proportion of the patients continued with MATADOR protocol at week 48. MATADOR protocol was discontinued upon disease flare or other reasons such as patients' request or severe adverse event (AE). Disease activities and structural changes were also evaluated.Results: Fifty-three patients fulfilled the entry criteria and were followed for 1-year. MATADOR protocol was continued for 1-year in 43 (81%) of the evaluated patients. Three patients experienced severe AEs. Mean DAS28-CRP and remission rate were 1.56 and 88% when ABT reduced and 1.80 and 81% at 1-year, respectively. Structural remission was achieved in 34 out of 42 evaluated patients.Conclusions: Reduced dose of intravenous ABT was proposed as a feasible choice for maintenance therapy for RA after achievement of remission/LDA, although further randomized trials would be awaited.
机译:目的:初步评估维持治疗的可行性,在实现缓解或低疾病活动(LDA)后,静脉注射(ABT)静脉内ABATACEPT(ABT)的静脉内ABATACEPT(ABT)至250mg /身体/月份的可行性。患者和方法:13位点治疗ABT治疗的RA患者在这一前瞻性介入试验研究中,2013年3月至2015年3月期间。纳入标准(1)年龄(1)年龄在20岁或以上,(2)在批准剂量的每月静脉内ABT治疗,(3)DAS28-CRP低于2.7至少6个月,(4)同意加入此审判,并在125公斤以下的书面知情同意书和(5)体重。注册的患者以静脉注射的每月ABT维持,减少250mg /体(Matador协议)。主要终点是患者在第48周继续进行骚动议定书的比例。在疾病爆发或其他原因如患者请求或严重不良事件(AE)上停止了Matador议定书。还评估了疾病活动和结构性变化。结果:五十三名患者均满足入境标准,遵循1年。在43名(81%)的评估患者中持续了仓司议定书。三名患者经历严重的AES。当ABT分别减少1.80%和81%时,平均DAS28-CRP和缓解率为1.56和88%。在42例评估患者中的34例中实现了结构缓解。结论:静脉内ABT的减少剂量作为RA在取得缓解/ LDA的成就后进行维持治疗的可行选择,尽管将等待进一步随机试验。

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