Zachariae Claus, Mørk Nils-Jørgen, Reunala Timo, Lorentzen Henrik, Falk Edvard, Karvonen Seija-Liisa, Johannesson Anders, Claréus Birgitta, Skov Lone, Mørk Gro, Walker Siân, Qvitzau Susanne
Department of Dermatology, Copenhagen University Hospital, Copenhagen, Denmark.
Acta Derm Venereol. 2008;88(5):495-501. doi: 10.2340/00015555-0511.
Many patients with moderate-to-severe plaque psoriasis do not respond adequately to methotrexate monotherapy. This pilot study, with a small patient population, was performed to evaluate the effectiveness and safety of etanercept and methotrexate combination in patients with plaque psoriasis and inadequate response to methotrexate. Outpatients with plaque psoriasis (Psoriasis Area and Severity Index > or = 8 and/or body surface area > 10%), despite methotrexate treatment (> or = 3 months; > or = 7.5 mg/week) were randomized to either etanercept with metho nottrexate tapered and discontinued (n = 28) or etanercept with continuous methotrexate (n = 31). Significantly more patients had a Physicians' Global Assessment of "clear"/"almost clear" in the combination group compared with etanercept/methotrexate taper (66.7 vs. 37.0%, respectively; p = 0.025). Adverse events were similar for both groups, with no cases of tuberculosis, malignancies or opportunistic infections reported. Addition of etanercept to methotrexate achieved significant improvement in psoriasis after 24 weeks.
许多中度至重度斑块状银屑病患者对甲氨蝶呤单药治疗反应欠佳。本项针对小样本患者群体的初步研究旨在评估依那西普与甲氨蝶呤联合用药对斑块状银屑病且对甲氨蝶呤反应不足患者的有效性和安全性。尽管接受了甲氨蝶呤治疗(≥3个月;≥7.5毫克/周),但斑块状银屑病门诊患者(银屑病面积和严重程度指数≥8和/或体表面积>10%)被随机分为两组,一组为依那西普联合逐渐减量并停用甲氨蝶呤(n = 28),另一组为依那西普联合持续使用甲氨蝶呤(n = 31)。与依那西普/甲氨蝶呤减量组相比,联合用药组中医生整体评估为“清除”/“几乎清除”的患者显著更多(分别为66.7%和37.0%;p = 0.025)。两组不良事件相似,均未报告结核病、恶性肿瘤或机会性感染病例。甲氨蝶呤联合依那西普治疗24周后银屑病有显著改善。