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首页> 外文期刊>Modern rheumatology >Long-term efficacy and safety of certolizumab pegol in Japanese rheumatoid arthritis patients with an inadequate response to methotrexate: 52-week results from an open-label extension of the J-RAPID study
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Long-term efficacy and safety of certolizumab pegol in Japanese rheumatoid arthritis patients with an inadequate response to methotrexate: 52-week results from an open-label extension of the J-RAPID study

机译:赛妥珠单抗聚乙二醇醚对甲氨蝶呤反应不良的日本类风湿性关节炎患者的长期疗效和安全性:J-RAPID研究的开放标签扩展结果为52周

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摘要

Objectives. To evaluate the long-term efficacy and safety of certolizumab pegol (CZP) plus methotrexate treatment and to assess the efficacy of two CZP maintenance dosing schedules in Japanese rheumatoid arthritis (RA) patients with an inadequate response to methotrexate. Methods. J-RAPID double-blind patients were entered into an open-label extension (OLE) study. Patients withdrawn due to lack of efficacy at 16 weeks and double-blind completers without a week-24 American College of Rheumatology (ACR) 20 response received CZP 200 mg every other week (Q2W) plus methotrexate. Double-blind completers with week-24 ACR20 responses were randomized to CZP 200 mg Q2W plus methotrexate or CZP 400 mg every 4 weeks plus methotrexate. Results. The ACR20/ACR50/ACR70 response rates of double-blind completers (n = 204) were 89.7%/67.2%/36.3% at OLE entry and 95.6%/84.8%/58.3% at 52 weeks, respectively. Other clinical, functional and radiographic outcomes were sustained with long-term CZP plus methotrexate. Long-term treatment with CZP was well-tolerated with no new unexpected adverse events observed. The efficacy and safety of CZP treatment were similar between the two dosing schedules. Conclusions. Continued CZP administration with methotrexate maintained efficacy over 52 weeks and was well-tolerated for Japanese RA patients. No obvious differences in clinical efficacy and safety were observed between the two dosing schedules, giving flexibility in maintenance administration schedules.
机译:目标。评估certolizumab聚乙二醇(CZP)联合甲氨蝶呤治疗的长期疗效和安全性,并评估两种对甲氨蝶呤反应不良的类风湿性关节炎(RA)患者的CZP维持给药方案的疗效。方法。 J-RAPID双盲患者进入了开放标签扩展(OLE)研究。因在16周时缺乏疗效而退出治疗的患者以及没有第24周的美国国立风湿病学会(ACR)20反应的双盲完成者,每隔一周(Q2W)加200毫克CZP加甲氨蝶呤。具有第24周ACR20反应的双盲完成者被随机分为CZP 200 mg Q2W加甲氨蝶呤或CZP 400 mg每4周加甲氨蝶呤。结果。双盲完成者(n = 204)的ACR20 / ACR50 / ACR70应答率在OLE进入时为89.7%/ 67.2%/ 36.3%,在52周时分别为95.6%/ 84.8%/ 58.3%。长期CZP加甲氨蝶呤可维持其他临床,功能和影像学结果。 CZP的长期治疗耐受性良好,未观察到新的意外不良事件。在两种给药方案之间,CZP治疗的疗效和安全性相似。结论连续服用甲氨蝶呤的CZP维持疗效超过52周,对日本RA患者耐受良好。两种给药方案之间在临床疗效和安全性上均未观察到明显差异,从而使维持给药方案具有灵活性。

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