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日本开始使用生物制剂治疗类风湿关节炎患者的多中心登记研究方案:Tsurumai 生物制剂通讯登记研究(TBCR 研究)。

Study protocol of a multicenter registry of patients with rheumatoid arthritis starting biologic therapy in Japan: Tsurumai Biologics Communication Registry (TBCR) study.

机构信息

Department of Orthopedic Surgery, Nagoya University, School of Medicine, 65 Tsurumai, Showa, Nagoya, Japan.

出版信息

Mod Rheumatol. 2012 Jun;22(3):339-45. doi: 10.1007/s10165-011-0518-4. Epub 2011 Sep 3.

Abstract

Biologic agents have proven to be effective against rheumatoid arthritis (RA) in clinical trials and post-marketing surveillance (PMS) studies. However, limited follow-up periods and strict criteria for recruitment might lead to an underestimation of adverse events. To document the long-term course of patients with RA treated with biologics in clinical settings, we established the Tsurumai Biologics Communication Registry (TBCR). First, we retrospectively collected data of patients registered for any biologic PMS study or clinical trial at participating institutes. Thus far, thirteen institutes have joined the registry and 860 patients have been identified. Comparing baseline characteristics by age and initiation year of biologics, young patients had significantly less joint damage and dysfunction and a higher dose of concomitant methotrexate (MTX) compared to older patients. Older age and functional class were significantly related to the incidence of adverse events that resulted in discontinuation of the 1st biologic treatment. The TBCR is in its initial stages, and information on all patients newly starting biologic therapy at participating institutes is being collected prospectively. Differences in baseline characteristics by age and initiation year of biologics need to be carefully evaluated in order to report on drug-related survival and long-term prognosis, using follow-up data in the near future.

摘要

生物制剂已被证明在临床试验和上市后监测 (PMS) 研究中对类风湿关节炎 (RA) 有效。然而,有限的随访期和招募的严格标准可能导致对不良事件的低估。为了记录在临床环境中使用生物制剂治疗的 RA 患者的长期病程,我们建立了 Tsurumai 生物制剂通讯登记处 (TBCR)。首先,我们回顾性地收集了参加研究所登记的任何生物 PMS 研究或临床试验的患者数据。迄今为止,已有 13 家研究所加入了该登记处,共确定了 860 名患者。按年龄和生物制剂起始年份比较基线特征,年轻患者的关节损伤和功能障碍明显较少,同时接受的甲氨蝶呤 (MTX) 剂量也较高。年龄较大和功能分级与导致首次生物治疗停药的不良事件的发生显著相关。TBCR 处于初始阶段,正在前瞻性地收集参加研究所新开始生物治疗的所有患者的信息。需要仔细评估生物制剂起始年龄和起始年份的基线特征差异,以便在不久的将来使用随访数据报告与药物相关的生存和长期预后。

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