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Updated systematic review and meta-analysis of randomized controlled trials comparing low- versus high-dose rituximab for rheumatoid arthritis

机译:比较低剂量和大剂量利妥昔单抗治疗类风湿关节炎的随机对照试验的最新系统评价和荟萃分析

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The purpose of this study is to update a systematic review and meta-analysis comparing low- (2 x 500 or 1 x 1000 mg) and high-dose (2 x 1000 mg) rituximab (RTX) for the treatment of rheumatoid arthritis (RA), considering the recent emergence of new evidence. The systematic literature review searching for randomized controlled trials (RCTs) was updated to November 6, 2014 using the PubMed, EMBASE, Cochrane Library, Web of Science databases, and hand searching. The primary outcomes were the American College of Rheumatology (ACR) criteria for 20 % improvement (ACR20), ACR50, and ACR70 responses and the Disease Activity Score in 28 joints (DAS28) at 24 and 48/52 weeks. The secondary outcomes were change in Health Assessment Questionnaire (HAQ) score, change in the radiographic modified Total Sharp Score (mTSS), levels of immunoglobulin G (IgG), and adverse events. In total, seven RCTs were identified, including two new full publication versions and one abstract of RCTs. There were no significant differences in the primary outcomes and change in HAQ, although the mean change in mTSS was 0.25 units (95 % CI, 0.01 to 0.49; P = 0.04) higher in low-dose group at week 52. Two RCTs did not demonstrate difference between the RTX regimens for maintaining clinical response (obtained initially using high-dose RTX) in anti-TNF-experienced patients. IgG levels were significantly higher (P a parts per thousand currency signaEuro parts per thousand 0.02), and first infusion reactions were less frequent in the low-dose group (P = 0.02). Our updated results further support the similar efficacy of both RTX regimens in different subsets of RA patients, demonstrating a better clinical and laboratory safety profile of the low-dose scheme.
机译:这项研究的目的是更新系统的综述和荟萃分析,比较低剂量(2 x 500或1 x 1000 mg)和大剂量(2 x 1000 mg)利妥昔单抗(RTX)治疗类风湿关节炎(RA) ),考虑到最近出现的新证据。使用PubMed,EMBASE,Cochrane图书馆,Web of Science数据库和人工搜索将系统化的文献综述搜索随机对照试验(RCT)更新至2014年11月6日。主要结果是美国风湿病学会(ACR)的20%改善标准(ACR20),ACR50和ACR70响应以及24和48/52周时28个关节的疾病活动评分(DAS28)。次要结果是健康评估问卷(HAQ)得分的变化,放射线照相修改的总锐利得分(mTSS)的变化,免疫球蛋白G(IgG)的水平以及不良事件的发生。总共确定了7个RCT,包括两个新的完整出版物版本和一个RCT摘要。尽管第52周低剂量组的mTSS平均变化高0.25个单位(95%CI,0.01至0.49; P = 0.04),但主要结局和HAQ的变化无显着差异。两个RCT均未证实了在抗TNF经验丰富的患者中,用于维持临床反应(最初使用大剂量RTX获得)的RTX方案之间存在差异。 IgG水平显着较高(P a /千货币符号欧元/千0.02),低剂量组的首次输注反应较少(P = 0.02)。我们更新的结果进一步支持了两种RTX方案在RA患者不同亚型中的相似疗效,证明了低剂量方案的更好的临床和实验室安全性。

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