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首页> 外文期刊>Arthritis research & therapy. >Comparative effectiveness and safety of rituximab versus subsequent anti–tumor necrosis factor therapy in patients with rheumatoid arthritis with prior exposure to anti–tumor necrosis factor therapies in the United States Corrona registry
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Comparative effectiveness and safety of rituximab versus subsequent anti–tumor necrosis factor therapy in patients with rheumatoid arthritis with prior exposure to anti–tumor necrosis factor therapies in the United States Corrona registry

机译:Rituximab与随后的抗肿瘤坏死因子治疗的对比效果和安全性关节炎患者,以前暴露于美国科罗拉州注册表的抗肿瘤坏死因子疗法

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Introduction: Patients with active rheumatoid arthritis (RA) despite anti–tumor necrosis factor(anti-TNF)agent treatment can switch to either a subsequent anti-TNF agent or a biologic with an alternative mechanism of action, such as rituximab; however, there are limited data available to help physicians decide between these 2 strategies. The objective of this analysis was to examine the effectiveness and safety of rituximab versus a subsequent anti-TNF agent in anti-TNF–experienced patients with RA using clinical practice data from the Corrona registry. Methods: Rituximab-naive patients from the Corrona registry with prior exposure to ≥1 anti-TNF agent who initiated rituximab or anti-TNF agents (2/28/2006-10/31/2012) were included. Two cohorts were analyzed: the trimmed population (excluding patients who fell outside the propensity score distribution overlap) and the stratified-matched population (stratified by 1 vs?≥2 anti-TNF agents, then matched based on propensity score). The primary effectiveness outcome was achievement of low disease activity (LDA)/remission (Clinical Disease Activity Index?≤10) at 1 year. Secondary outcomes included achievement of modified American College of Rheumatology (mACR) 20/50/70 responses and meaningful improvement (≥0.25) in modified Health Assessment Questionnaire (mHAQ) score at 1 year. New cardiovascular, infectious and cancer events were reported. Results: Estimates for LDA/remission, mACR response and mHAQ improvement were consistently better for rituximab than for anti-TNF agent users in adjusted analyses. The odds ratio for likelihood of LDA/remission in rituximab versus anti-TNF patients was 1.35 (95 % CI, 0.95-1.91) in the trimmed population and 1.54 (95 % CI, 1.01-2.35) in the stratified-matched population. Rituximab patients were significantly more likely than anti-TNF patients to achieve mACR20/50 and mHAQ improvement in the trimmed population and mACR20 and mHAQ in the stratified-matched population. The rate of new adverse events per 100 patient-years was similar between groups. Conclusions: In anti-TNF–experienced patients with RA, rituximab was associated with an increased likelihood of achieving LDA/remission, mACR response and physical function improvement, with a comparable safety profile, versus subsequent anti-TNF agent users.
机译:介绍:患有活性类风湿性关节炎(RA)尽管抗肿瘤坏死因子(抗TNF)剂治疗,可以切换到随后的抗TNF剂或生物学,替代的作用机制,例如Rituximab;但是,有限的数据可用于帮助医生在这2战略之间决定。该分析的目的是检测利妥昔单抗与随后的抗TNF经验丰富的RA患者的抗TNF剂的有效性和安全性,使用来自Corrona登记处的临床实践数据。方法:列入Ritona Registry的Rituximab-naive患者,≥1种引发Rituximab或抗TNF药剂(2/88 / 28 / 2006-10/31 / 2012)的≥1抗TNF试剂。分析了两个群组:修剪的人口(不包括俯卧位得分分布重叠的患者)和分层匹配的人群(分层1 VS?≥2抗TNF试剂,然后基于倾向得分匹配)。主要有效性结果是在1年内实现低疾病活动(LDA)/缓解(临床疾病活动指数?≤10)。二次结果包括改性美国风湿病学院(MACR)20/50/70的成就,改进的健康评估问卷(MHAQ)评分在1年的响应和有意义的改善(≥0.25)。报道了新的心血管,传染病和癌症事件。结果:LDA /缓解,MACR响应和MHAQ改善的估计对于Rituximab而言,Rituximab始终比调整后分析中的抗TNF代理用户更好。 Rituximab与抗TNF患者的LDA /缓解可能性的可能性比率为1.35(95%CI,0.95-1.91),在分层匹配的人群中,1.54(95%CI,1.01-2.35)。 Rituximab患者的可能性比抗TNF患者更容易获得MacR20 / 50和MHAQ在分层匹配群体中的修剪群体和MAMR20和MHAQ的改善。每100名患者年的新不良事件率在群体之间相似。结论:在抗TNF经验丰富的RA患者中,利妥昔单抗与实现LDA /缓解,MACR响应和物理功能改进的可能性增加有关,具有可比的安全性,与后续的抗TNF代理商用户。

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