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首页> 外文期刊>Rheumatology international. >Safety and effectiveness of switching from infliximab to etanercept in patients with rheumatoid arthritis: Results from a large Japanese postmarketing surveillance study
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Safety and effectiveness of switching from infliximab to etanercept in patients with rheumatoid arthritis: Results from a large Japanese postmarketing surveillance study

机译:类风湿关节炎患者从英夫利昔单抗转为依那西普的安全性和有效性:一项大型日本上市后监测研究的结果

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Finding an effective treatment strategy for rheumatoid arthritis (RA) patients who have not benefited from previous tumor necrosis factor-α antagonist treatment is important for minimizing RA disease activity and improving patient outcomes. The aim of this study was to compare the safety and effectiveness of etanercept in patients with and without infliximab (IFX) treatment experience. Patients (n = 7,099) from a large postmarketing observational study of etanercept use in Japan were divided into 2 cohorts based on previous IFX use (pre-IFX and non-IFX). Baseline characteristics were assessed in each cohort. Adverse events (AEs) and European League Against Rheumatism (EULAR) responses were monitored every 4 weeks for 24 weeks. At baseline, pre-IFX patients were younger and had fewer comorbidities and a shorter RA duration than non-IFX patients. During the study, pre-IFX patients received concomitant methotrexate more often than non-IFX patients. The incidence of AEs and serious AEs were significantly lower in pre-IFX patients, as was the percentage of patients who discontinued treatment. Both cohorts had significant improvement (P<0.001) in EULAR responses at the end of the treatment period. This study demonstrated that etanercept was effective and well tolerated in active RA patients with and without prior IFX treatment.
机译:对于未从先前的肿瘤坏死因子-α拮抗剂治疗中受益的类风湿关节炎(RA)患者,寻找有效的治疗策略对于最大程度地减少RA疾病活动并改善患者预后至关重要。这项研究的目的是比较依那西普在有无英夫利昔单抗(IFX)治疗经验的患者中的安全性和有效性。来自日本一项大型的依那西普使用的上市后观察研究的患者(n = 7,099)根据以前的IFX使用情况(IFX之前和非IFX)分为两个队列。在每个队列中评估基线特征。每4周监测一次不良事件(AEs)和欧洲抗风湿联盟(EULAR)反应,持续24周。基线时,IFX之前的患者比非IFX的患者年轻,合并症少,RA病程短。在研究期间,IFX之前的患者比非IFX的患者接受甲氨蝶呤的频率更高。在IFX之前的患者中,AEs和严重AEs的发生率显着降低,而中止治疗的患者百分比也是如此。在治疗期结束时,两个队列的EULAR反应均显着改善(P <0.001)。这项研究表明依那西普在接受或不接受IFX治疗的活跃RA患者中有效且耐受性良好。

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