Yuasa Shino, Yamaguchi Harutaka, Nakanishi Yoshinori, Kawaminami Shingo, Tabata Ryo, Shimizu Nobuhiko, Kohno Mitsuhiro, Shimizu Teruki, Miyata Junya, Nakayama Mayuko, Kishi Jun, Toyoda Yuko, Nishioka Yasuhiko, Tani Kenji
Department of General Medicine, Institute of Health Biosciences, the University of Tokushima Graduate School, Tokushima, Japan.
J Med Invest. 2013;60(1-2):77-90. doi: 10.2152/jmi.60.77.
Biological agents represent an important advancement in for the treatment of rheumatoid arthritis (RA), but there is a subset of patients who do not improve despite therapy. This study aimed to determine the efficacy of biological agents for RA and to identify clinical factors that are associated with their response. We studied 98 patients with RA who started an initiating biological agent which was selected from infliximab, etanercept, adalimumab and tociliximab at 4 medical institutions. Etanercept was the most frequently used biological agent followed by infliximab although there was a difference in the selection of the biological agents among medical institutions. We found that etanercept achieved the highest treatment response, remission rate and drug survival rate. A high disease activity in the baseline disease activity score-c-reactive protein (CRP) was shown to be a negative predictor of the treatment response, and high patient global assessment was significantly less likely to achieve a good response. At week 4, decreases in 28 swollen joint counts and CRP were useful as predictors for sustaining the efficacy up to week 48. These data demonstrate that assessments of the disease activity at baseline and the early treatment response may be useful in predicting the efficacy and drug survival rate of biological agents.
生物制剂是类风湿关节炎(RA)治疗方面的一项重要进展,但有一部分患者尽管接受了治疗仍无改善。本研究旨在确定生物制剂对RA的疗效,并识别与其反应相关的临床因素。我们研究了98例在4家医疗机构开始使用生物制剂的RA患者,这些生物制剂选自英夫利昔单抗、依那西普、阿达木单抗和托珠单抗。依那西普是最常用的生物制剂,其次是英夫利昔单抗,不过各医疗机构在生物制剂的选择上存在差异。我们发现依那西普实现了最高的治疗反应率、缓解率和药物生存率。基线疾病活动评分 - C反应蛋白(CRP)中的高疾病活动度被证明是治疗反应的负性预测指标,而高患者整体评估得分者显著不太可能获得良好反应。在第4周时,28个肿胀关节计数和CRP的下降可作为预测持续疗效直至第48周的指标。这些数据表明,基线疾病活动度评估和早期治疗反应可能有助于预测生物制剂的疗效和药物生存率。