首页> 外文OA文献 >POSSIBILITIES FOR PRESERVING THE RESULTS OF TREATMENT IN PATIENTS WITH ACTIVE RHEUMATOID ARTHRITIS AFTER DOSE REDUCTION AND/OR DISCONTINUATION OF BIOLOGICAL AGENTS: A REMARCA STUDY
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POSSIBILITIES FOR PRESERVING THE RESULTS OF TREATMENT IN PATIENTS WITH ACTIVE RHEUMATOID ARTHRITIS AFTER DOSE REDUCTION AND/OR DISCONTINUATION OF BIOLOGICAL AGENTS: A REMARCA STUDY

机译:在剂量减少和/或停止生物药物后,保留有活性类风湿性关节炎患者治疗结果的可能性:REMARCA研究

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摘要

Russian and international clinical recommendations postulate the possibility of withdrawal of biological agents in patients with rheumatoid arthritis (RA) after the achievement of clinical remission. But it is not clear what would be the results of implementation of these recommendations in clinical practice.Patients and methods. In REMARCA (Russian invEstigation of MethotrexAte and biologicals for eaRly aCtive Arthritis) trial 78 patients (66 females, 12 males, median age 53 years, duration of disease 7 months at inclusion), who were resistant to high doses of subcutaneous (SC) methotrexate (MTX), were treated by combination therapy with SC MT and biologics (adalimumab, certolizumab or abatacept). Patients were investigated every 3 months using DAS28-ESR, SDAI, CDAI indices as disease activity measures.Results. 30 (38.5%) patients (from 78) continued combination therapy. In 47 (60.3%) after achievement of remission or low disease activity (LDA) the therapy was modified to one of two options: 1) in 21 (26.9%) patients doses of biologics were tapered, in some cases to zero; 2) in 26 (33.3%) patients single-step discontinuation of biologics was performed. After 6 months among 47 patients with modification of therapy 27 (57.4%) maintained remission or LDA, in 20 (42.6%) deterioration observed, including 6 (12.8%) patients who lost remission but remained in LDA, and 14 (29.8%) flared (activity increased to moderate or high levels). First modification option was significantly superior to second option regarding the maintaining remission or LDA.Conclusion. In terms of maximum preservation of the results, optimal modification of treatment strategy is the tapering of the dose by the gradual increase in the period between injections of biologics, at least 12 months after reaching the state LDA or clinical remission.
机译:俄罗斯和国际临床推荐假设在实现临床缓解后的类风湿性关节炎(RA)患者中戒断生物药物的可能性。但目前尚不清楚在临床实践中实施这些建议的结果.Patient和方法。在Remarca(俄罗斯对早期活跃性关节炎的甲氨蝶呤和生物学的甲氨酸类药物调查)试验78例患者(66名女性,12名男性,53岁,含有疾病的持续时间),耐受高剂量的皮下(SC)甲氨蝶呤(MTX)通过用SC MT和生物学(Adalimalab,Certolizumab或Abatacept)进行治疗治疗。使用DAS28-ESR,SDAI,CDAI指数作为疾病活动措施,每3个月调查一次患者。结果。 30(38.5%)患者(78)持续的联合治疗。在47(60.3%)在实现缓解或低疾病活动(LDA)后,治疗被修改为两种选择中的一种:1)在21例(26.9%)患者中,生物学剂量逐渐变细,在某些情况下为零; 2)在26例(33.3%)患者中进行了单步停药生物制剂。在6个月后,47例治疗修饰患者27(57.4%)保持缓解或LDA,观察到20(42.6%)恶化,其中6名(12.8%)患者失去缓解但仍然存在于LDA,14岁(29.8%) Flared(活性增加至中度或高水平)。第一修饰选项明显优于关于保持缓解或LDA的第二种选择。结论。就结果的最大保存而言,治疗策略的最佳改性是通过在达到状态LDA或临床缓解后至少12个月的生物学期间逐渐增加的剂量逐渐变细。

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