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银屑病生物制剂的转换:原因和结果。

Switching of biologics in psoriasis: Reasons and results.

机构信息

Department of Dermatology, The Jikei University School of Medicine, Tokyo, Japan.

出版信息

J Dermatol. 2017 Sep;44(9):1015-1019. doi: 10.1111/1346-8138.13860. Epub 2017 May 10.

Abstract

Efficacy and safety profiles of biologics have been established for moderate to severe psoriasis. However, inefficacy or adverse events sometimes require changing the treatment to other biologics. Here, we examine the effectiveness of this strategy. We retrospectively investigated cases requiring switching biologics. We enrolled 275 psoriatic patients treated with biologics between January 2010 and December 2014 in our hospital. Of these, 51 required a switch to another biologic. First-line therapies were infliximab (IFX, n = 26), adalimumab (ADA, n = 18) and ustekinumab (UST, n = 7), and second-line therapies were IFX (n = 5), ADA (n = 21) and UST (n = 25). Reasons for switching were inefficacy (n = 38), adverse events (n = 11) and others (n = 2). The details were primary failure (n = 15), secondary failure (n = 23) and infusion reactions (n = 8). In 49 patients who switched biologics due to inefficacy and adverse events, the mean Psoriasis Area and Severity Index (PASI) score at week 16 was 4.3 for first-line therapies and 2.9 for second-line therapies (P < 0.05). Switching to a second biologic therapy to address the first's inefficacy or adverse events often results in significant improvement in moderate to severe psoriasis.

摘要

生物制剂在中重度银屑病中的疗效和安全性已得到证实。然而,有时无效或出现不良反应会导致需要更换为其他生物制剂。在此,我们研究了这种策略的有效性。我们回顾性地调查了需要转换生物制剂的病例。我们招募了 2010 年 1 月至 2014 年 12 月期间在我院接受生物制剂治疗的 275 例银屑病患者。其中 51 例需要转换为另一种生物制剂。一线治疗药物为英夫利昔单抗(IFX,n = 26)、阿达木单抗(ADA,n = 18)和乌司奴单抗(UST,n = 7),二线治疗药物为 IFX(n = 5)、ADA(n = 21)和 UST(n = 25)。转换的原因是无效(n = 38)、不良反应(n = 11)和其他原因(n = 2)。具体原因包括原发失效(n = 15)、继发失效(n = 23)和输注反应(n = 8)。在因无效和不良反应而转换生物制剂的 49 例患者中,一线治疗第 16 周的银屑病面积和严重程度指数(PASI)评分平均为 4.3,二线治疗的评分平均为 2.9(P < 0.05)。针对一线药物的无效或不良反应,换用二线生物制剂治疗通常会显著改善中重度银屑病。

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