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聚乙二醇化赛妥珠单抗在无法接受甲氨蝶呤治疗的日本类风湿关节炎患者中的长期疗效和安全性:HIKARI研究开放标签扩展的52周结果

Long-term efficacy and safety of certolizumab pegol in Japanese rheumatoid arthritis patients who could not receive methotrexate: 52-week results from an open-label extension of the HIKARI study.

作者信息

Tanaka Yoshiya, Yamamoto Kazuhiko, Takeuchi Tsutomu, Yamanaka Hisashi, Ishiguro Naoki, Eguchi Katsumi, Watanabe Akira, Origasa Hideki, Shoji Toshiharu, Miyasaka Nobuyuki, Koike Takao

机构信息

First Department of Internal Medicine, University of Occupational and Environmental Health, Japan , Kitakyushu, Fukuoka , Japan.

出版信息

Mod Rheumatol. 2014 Sep;24(5):725-33. doi: 10.3109/14397595.2013.865822. Epub 2013 Dec 29.

Abstract

OBJECTIVES

To evaluate the long-term efficacy and safety of certolizumab pegol (CZP) treatment and to assess the efficacy of two CZP maintenance dosing schedules in Japanese rheumatoid arthritis (RA) patients who could not receive methotrexate (MTX).

METHODS

HIKARI double-blind (DB) patients were entered into an open-label extension (OLE) study. Patients withdrawn at 16 weeks due to lack of efficacy and DB completers without a 24-week American College of Rheumatology (ACR)20 response received CZP 200 mg every 2 weeks (Q2W). DB completers with 24-week ACR20 responses were randomized to CZP 200 mg Q2W or CZP 400 mg every 4 weeks.

RESULTS

The ACR20/ACR50/ACR70 response rates of DB completers (n = 98) were 82.7%/56.1%/34.7% at OLE entry, and 83.7%/65.3%/48.0% at 52 weeks, respectively. Other clinical, functional, and radiographic outcomes were sustained during long-term administration of CZP, even without MTX. No new unexpected adverse events were observed during long-term CZP treatment. The efficacy and safety of CZP treatment were similar between the two dosing schedules.

CONCLUSIONS

Long-term CZP administration is efficacious and safe for RA patients. No obvious differences in clinical efficacy and safety were observed between the two dosing schedules. The choice between two maintenace regimens adds flexibility in administration schedules for RA patients and physicians.

摘要

目的

评估聚乙二醇化赛妥珠单抗(CZP)治疗的长期疗效和安全性,并评估两种 CZP 维持给药方案对无法接受甲氨蝶呤(MTX)治疗的日本类风湿关节炎(RA)患者的疗效。

方法

HIKARI 双盲(DB)患者进入开放标签扩展(OLE)研究。因疗效不佳在 16 周时退出的患者以及未达到 24 周美国风湿病学会(ACR)20 反应的双盲完成者每 2 周接受 200 mg CZP(Q2W)。达到 24 周 ACR20 反应的双盲完成者被随机分为每 2 周接受 200 mg CZP 或每 4 周接受 400 mg CZP。

结果

双盲完成者(n = 98)在 OLE 入组时的 ACR20/ACR50/ACR70 反应率分别为 82.7%/56.1%/34.7%,在 52 周时分别为 83.7%/65.3%/48.0%。即使未使用 MTX,在 CZP 长期给药期间,其他临床、功能和影像学结果也得以维持。在 CZP 长期治疗期间未观察到新的意外不良事件。两种给药方案之间 CZP 治疗的疗效和安全性相似。

结论

长期给予 CZP 对 RA 患者有效且安全。两种给药方案在临床疗效和安全性方面未观察到明显差异。两种维持方案的选择为 RA 患者和医生在给药方案上增加了灵活性。

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