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首页> 外文期刊>British Journal of Dermatology >A randomized, double-blind, placebo-controlled study to evaluate the addition of methotrexate to etanercept in patients with moderate to severe plaque psoriasis
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A randomized, double-blind, placebo-controlled study to evaluate the addition of methotrexate to etanercept in patients with moderate to severe plaque psoriasis

机译:一项随机,双盲,安慰剂对照研究,评估中度至重度斑块状牛皮癣患者在依那西普中加用氨甲蝶呤

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Background Etanercept plus methotrexate combination therapy has not been adequately investigated in psoriasis. Objectives To evaluate etanercept plus methotrexate vs. etanercept monotherapy in patients with moderate to severe plaque psoriasis who had not failed prior methotrexate or tumour necrosis factor-inhibitor therapy. Methods Patients received etanercept 50 mg twice weekly for 12 weeks followed by 50 mg once weekly for 12 weeks and were randomized 1: 1 to receive methotrexate (7·5-15 mg weekly) or placebo. The primary endpoint was the proportion of patients achieving ≥75% improvement in Psoriasis Area and Severity Index (PASI 75) at week 24. Results In total, 239 patients were enrolled in each arm. PASI 75 was significantly higher at week 24 for the combination therapy group compared with the monotherapy group (77·3% vs. 60·3%; P < 0·0001). Other PASI improvement scores at week 12 [PASI 75, 70·2% vs. 54·3% (P = 0·01); PASI 50, 92·4% vs. 83·8% (P = 0·01); and PASI 90, 34·0% vs. 23·1% (P = 0·03)] showed similar results as did week 24 PASI 50 (91·6% vs. 84·6%; P = 0·01) and PASI 90 (53·8% vs. 34·2%; P = 0·01). Significantly more patients receiving combination therapy than monotherapy had static Physician's Global Assessment of clear/almost clear at week 12 (65·5% vs. 47·0%; P = 0·01) and week 24 (71·8% vs. 54·3%; P = 0·01). Adverse events (AEs) were reported in 74·9% and 59·8% of combination therapy and monotherapy groups, respectively; three serious AEs were reported in each arm. Conclusions Combination therapy with etanercept plus methotrexate had acceptable tolerability and increased efficacy compared with etanercept monotherapy in patients with moderate to severe psoriasis.
机译:背景Etanercept联合甲氨蝶呤联合治疗尚未在牛皮癣中得到充分研究。目的评估依那西普联合氨甲蝶呤与依那西普单药治疗在未曾接受甲氨蝶呤或肿瘤坏死因子抑制剂治疗失败的中度至重度斑块状牛皮癣患者中的应用。方法患者接受伊那西普50 mg每周12次,然后每周50 mg一次12周,并按1:1的比例随机分配接受甲氨蝶呤(每周7·5-15 mg)或安慰剂。主要终点指标是在第24周时银屑病面积和严重性指数(PASI 75)改善≥75%的患者比例。结果总共有239名患者参加了每组研究。与单一疗法组相比,联合疗法组在第24周的PASI 75显着更高(77·3%vs. 60·3%; P <0·0001)。第12周的其他PASI改善评分[PASI 75,70·2%vs. 54·3%(P = 0·01); PASI 50,92·4%和83·8%(P = 0·01); PASI 90、34·0%和23·1%(P = 0·03)的结果与第24周PASI 50相似(91·6%和84·6%; P = 0·01), PASI 90(53·8%与34·2%; P = 0·01)。与单纯疗法相比,接受联合治疗的患者明显多于在第12周(65·5%对47·0%; P = 0·01)和第24周(对71/8%对54)的静态/整体清晰的静态医师全球评估·3%; P = 0·01)。联合治疗组和单一治疗组的不良事件(AE)分别为74·9%和59·8%。每只手臂报告了三个严重的不良事件。结论与依那西普单药治疗相比,依那西普联合甲氨蝶呤治疗中重度银屑病具有较好的耐受性和疗效。

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