Matsuno Hiroaki
Matsuno Clinic for Rheumatic Diseases, Kureha-cho, Toyama city, Toyama, Japan, and Institute of Medical Science, Tokyo Medical University , Tokyo , Japan.
Mod Rheumatol. 2015 Jan;25(1):38-42. doi: 10.3109/14397595.2014.915073.
To optimize the efficacy of treatment with tocilizumab for rheumatoid arthritis (RA), we comparatively analyzed the outcome of tocilizumab treatment in patients with normal background changes associated closely with IL-6.
The study involved 87 patients with RA satisfying the diagnostic criteria of the American College of Rheumatology (ACR) and receiving continuous tocilizumab treatment for 24 weeks or longer. The outcome of tocilizumab treatment in these patients was comparatively analyzed in relation to the baseline platelet count (the high platelet count group and the normal group), pretreatment hemoglobin levels (the low group and the normal platelet count group), and speed of bone destruction (the rapid progression group and slow progression group).
Treatment with tocilizumab significantly improved the 28-joint disease activity score using the erythrocyte sedimentation rate (DAS28-ESR) and Clinical Disease Activity Index (CDAI), regardless of baseline platelet count, hemoglobin level, or annual speed of bone destruction (ΔTSS). The margins of improvement in DAS28-ESR and CDAI did not differ depending on baseline hemoglobin level or ΔTSS, but the improvement was significantly greater in the high platelet count group than in the normal platelet count group.
These results suggest that in patients with high platelet count, IL-6 is a more important factor involved in RA pathogenesis and that tocilizumab is suitable as a first-line biologic for the treatment of RA patients with high platelet count.
为优化托珠单抗治疗类风湿关节炎(RA)的疗效,我们比较分析了托珠单抗治疗在与IL-6密切相关的正常背景变化患者中的治疗结果。
该研究纳入了87例符合美国风湿病学会(ACR)诊断标准且接受托珠单抗持续治疗24周或更长时间的RA患者。对这些患者托珠单抗治疗的结果,根据基线血小板计数(高血小板计数组和正常组)、治疗前血红蛋白水平(低水平组和正常血小板计数组)以及骨破坏速度(快速进展组和缓慢进展组)进行了比较分析。
无论基线血小板计数、血红蛋白水平或每年骨破坏速度(ΔTSS)如何,托珠单抗治疗均显著改善了使用红细胞沉降率的28关节疾病活动评分(DAS28-ESR)和临床疾病活动指数(CDAI)。DAS28-ESR和CDAI的改善幅度不因基线血红蛋白水平或ΔTSS而有所不同,但高血小板计数组的改善显著大于正常血小板计数组。
这些结果表明,在高血小板计数的患者中,IL-6是参与RA发病机制的更重要因素,并且托珠单抗适合作为治疗高血小板计数RA患者的一线生物制剂。