Papp K A, Barber K, Bissonnette R, Bourcier M, Lynde C W, Poulin Y, Shelton J, Toole J, Vieira A, Poulin-Costello M
Probity Medical Research, Waterloo, ON, Canada.
Kirk Barber Research, Calgary, AB, Canada.
J Eur Acad Dermatol Venereol. 2015 Feb;29(2):361-366. doi: 10.1111/jdv.12555. Epub 2014 Jul 1.
Topical corticosteroids are used with systemic therapies for treatment of plaque psoriasis, but data from randomized clinical trials to document efficacy of combination therapy are lacking.
To evaluate efficacy and safety of adding topical corticosteroid therapy from the time that etanercept dosage is reduced from initial label dose [50 mg twice weekly (BIW)] to maintenance dose [50 mg once weekly (QW)].
In this phase 3b, multicentre, randomized, open-label study, patients with moderate-to-severe plaque psoriasis received etanercept 50 mg BIW for 12 weeks, and then were randomized to etanercept 50 mg BIW or 50 mg QW plus topical agent as needed to achieve static physician global assessment (sPGA) status of clear for 12 weeks. Endpoints included percentage change in Psoriasis Area and Severity Index (PASI) score from week 12 to week 24 (primary endpoint); proportion of patients achieving 50% improvement in (PASI 50), PASI 75 and PASI 90; patients achieving sPGA of clear/almost clear; and change in affected body surface area (BSA).
Mean difference [95% confidence interval (CI)] between etanercept arm (n = 140) and etanercept plus topical arm (n = 142) in change in PASI score from week 12 to week 24 was 16.2% (-3.5%, 35.8%). PASI response rates were similar between groups. Percentage (95% CI) of patients achieving sPGA status of clear/almost clear was 40.6% (32.5%, 48.6%) and 45.8% (37.6%, 54.0%) at week 12 for patients in etanercept and etanercept plus topical arms, respectively, and 53.5% (45.3%, 61.7%) and 45.4% (37.2%, 53.6%) at week 24. Difference (95% CI) between groups in change in affected BSA from week 12 to week 24 was 4.9% (-23.4%, 33.2%).
Patients who received etanercept 50 mg QW at week 12 plus as-needed topical therapy and those who stayed on etanercept 50 mg BIW maintained clinical response through week 24 with no notable differences in PASI responses.
外用皮质类固醇与全身治疗联合用于斑块状银屑病的治疗,但缺乏随机临床试验数据来证明联合治疗的疗效。
评估从依那西普剂量从初始标签剂量[每周两次50mg(BIW)]减至维持剂量[每周一次50mg(QW)]时开始加用外用皮质类固醇治疗的疗效和安全性。
在这项3b期、多中心、随机、开放标签研究中,中度至重度斑块状银屑病患者接受依那西普每周两次50mg治疗12周,然后随机分为依那西普每周两次50mg组或每周一次50mg依那西普加按需使用的外用药物组,以达到静态医师整体评估(sPGA)为清除状态并维持12周。终点包括银屑病面积和严重程度指数(PASI)评分从第12周至第24周的变化百分比(主要终点);达到PASI改善50%(PASI 50)、PASI 75和PASI 90的患者比例;达到sPGA清除/几乎清除的患者;以及受累体表面积(BSA)的变化。
依那西普组(n = 140)和依那西普加外用药物组(n = 142)从第12周至第24周PASI评分变化的平均差异[95%置信区间(CI)]为16.2%(-3.5%,35.8%)。两组间PASI反应率相似。依那西普组和依那西普加外用药物组患者在第12周达到sPGA清除/几乎清除状态的百分比(95%CI)分别为40.6%(32.5%,48.6%)和45.8%(37.6%,54.0%),在第24周分别为53.5%(45.3%,61.7%)和45.4%(37.2%,53.6%)。两组从第12周至第24周受累BSA变化的差异(95%CI)为4.9%(-23.4%,33.2%)。
在第12周接受每周一次50mg依那西普加按需外用治疗的患者和继续接受每周两次50mg依那西普治疗的患者在第24周时均维持临床反应,PASI反应无显著差异。