首页> 外文期刊>Value in health: the journal of the International Society for Pharmacoeconomics and Outcomes Research >Long-Term Efficacy of Etanercept for Plaque-Type Psoriasis and Estimated Cost in Daily Clinical Practice
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Long-Term Efficacy of Etanercept for Plaque-Type Psoriasis and Estimated Cost in Daily Clinical Practice

机译:依那西普对斑块型牛皮癣的长期疗效和每日临床实践中的估计成本

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Background: There are numerous clinical trials proving efficacy and safety profiles of etanercept. Newer studies, however, include patients with significant comorbidities, unstable psoriasis, or concomitant treatments. Objective: The objective of this study was to provide data on long-term response to etanercept and estimate the cost in daily practice. Methods: This is an observational retrospective study including patients with plaque-type psoriasis receiving etanercept 50 mg/wk for more than 6 months at the Dermatology Department of the University Hospital of La Corutia (Spain). Psoriasis severity was determined using the Psoriasis Area and Severity Index (PASI) at baseline and then at 12 weeks, 24 weeks, and annually until treatment discontinuation. Results: A total of 102 patients aged 24 to 78 years were included. Response rates of 58.8% and 66.3% for PASI 75 score (reduction of at least 75% in PASI score compared with baseline) were achieved after 12 and 24 weeks of treatment, respectively. Among patients who continued treatment, the PASI 75 score was maintained by 75.3% at 1 year, 82.5% at 2 years, and 88.2% at 3 years. The percentage of patients receiving other systemic treatments was 38.2%. Adverse effects were reported in 13.7%, all of them mild, except one case of urinary sepsis. The average cost per patient was (sic)244.68 +/- (sic)45.27 per week and (sic)34.95 +/- (sic)6.46 per day. Conclusions: We provide data on long-term response to etanercept and its costs in a real-world setting. Response rates were higher than in some clinical trials, with progressive efficacy and not related to body mass index. Etanercept cost was comparable with that estimated in other studies. Combination with a conventional systemic agent can enhance efficacy without additional adverse events.
机译:背景:有大量临床试验证明依那西普的疗效和安全性。但是,较新的研究包括合并症严重,牛皮癣不稳定或同时接受治疗的患者。目的:本研究的目的是提供对依那西普的长期反应的数据,并估算日常使用的费用。方法:这是一项观察性回顾性研究,包括在西班牙拉科鲁蒂亚大学医院皮肤科接受依那西普50 mg / wk接受6个月以上依那西普治疗的斑块型牛皮癣患者。使用银屑病面积和严重程度指数(PASI)在基线,然后在12周,24周以及每年直至停止治疗之前使用银屑病面积和严重性指数(PASI)确定牛皮癣的严重程度。结果:共纳入102例24至78岁的患者。治疗12周和24周后,PASI 75评分的缓解率分别为58.8%和66.3%(与基线相比,PASI评分至少降低了75%)。在继续治疗的患者中,PASI 75评分在1年时保持75.3%,在2年时保持82.5%,在3年时保持88.2%。接受其他全身治疗的患者比例为38.2%。不良反应报告为13.7%,除一例尿败血症外,其余均为轻度。每位患者的平均费用为每周(sic)244.68 +/-(sic)45.27和每天(sic)34.95 +/-(sic)6.46。结论:我们提供了在实际环境中对依那西普的长期反应及其成本的数据。缓解率高于某些临床试验,具有渐进疗效,且与体重指数无关。依那西普的费用与其他研究估计的费用相当。与常规全身性药物合用可提高疗效,而不会产生其他不良事件。

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