van der Heijde D, Burmester G, Melo-Gomes J, Codreanu C, Mola E Martin, Pedersen R, Freundlich B, Chang D J
Leiden University Medical Center, PO Box 9600, 2300RC Leiden, The Netherlands.
Ann Rheum Dis. 2008 Feb;67(2):182-8. doi: 10.1136/ard.2007.076166. Epub 2007 Aug 29.
To determine if adding etanercept (ETN) to methotrexate (MTX) or MTX to ETN for 52 weeks in rheumatoid arthritis (RA) patients with moderate disease activity provides higher efficacy.
All patients (n = 227) received open-label ETN 25 mg subcutaneously twice-weekly and MTX orally up to 20 mg weekly for 52 weeks and had completed a 3-year study in which patients received MTX, ETN or combination therapy. Endpoints were based on Disease Activity Score (DAS) and European League Against Rheumatism (EULAR) responses.
Patients previously receiving combination therapy (Combination group; n = 96) had a lower disease activity at baseline. The mean DAS for those previously receiving MTX (ETN-added group; n = 55) and previously receiving ETN (MTX-added group; n = 76) were in the moderate disease activity range at baseline; Combination patients had a low disease activity. The greatest increase in DAS remission rates from baseline to week 52 was in the ETN-added group (23.6% to 41.8%, p<0.01), although Combination (37.6% to 50.0%, p<0.01) and MTX-added (26.7% to 36.8%, p = NS) also demonstrated improvements. DAS low disease activity and EULAR responses showed similar results. No new safety issues were identified.
RA patients who were partial responders to long-term MTX or etanercept monotherapy obtained a higher efficacy with combination therapy. Responses achieved by patients with combination therapy after 3 years in the previous study were sustained or improved during the fourth year of treatment. This trial supports the higher therapeutic effect of combination treatment with etanercept and MTX in RA patients with moderate disease activity despite monotherapy with one of the two agents.
确定在中度疾病活动的类风湿关节炎(RA)患者中,将依那西普(ETN)添加到甲氨蝶呤(MTX)中或把MTX添加到ETN中治疗52周是否能提供更高的疗效。
所有患者(n = 227)接受开放标签的ETN皮下注射,每周两次,每次25mg,口服MTX,每周最多20mg,共52周,并完成了一项为期3年的研究,在此研究中患者接受MTX、ETN或联合治疗。终点基于疾病活动评分(DAS)和欧洲抗风湿病联盟(EULAR)反应。
先前接受联合治疗的患者(联合治疗组;n = 96)在基线时疾病活动度较低。先前接受MTX治疗的患者(添加ETN组;n = 55)和先前接受ETN治疗的患者(添加MTX组;n = 76)在基线时的平均DAS处于中度疾病活动范围内;联合治疗组患者疾病活动度较低。从基线到第52周,DAS缓解率增加最大的是添加ETN组(23.6%至41.8%,p<0.01),尽管联合治疗组(37.6%至50.0%,p<0.01)和添加MTX组(26.7%至36.8%,p =无统计学意义)也显示出改善。DAS低疾病活动度和EULAR反应显示出类似结果。未发现新的安全问题。
对长期MTX或依那西普单药治疗部分有反应的RA患者,联合治疗疗效更高。在前一项研究中联合治疗患者三年后取得的反应在治疗第四年得以维持或改善。该试验支持在中度疾病活动的RA患者中,依那西普和MTX联合治疗比两种药物之一的单药治疗具有更高的治疗效果。