医学
乌斯特基努马
阿达木单抗
不利影响
英夫利昔单抗
银屑病
银屑病面积及严重程度指数
内科学
皮肤病科
第一行
疾病
作者
Hiromi Honda,Yoshinori Umezawa,Sota Kikuchi,Koichi Yanaba,Osamu Fukuchi,Toshihiro Ito,Yoshimasa Nobeyama,Akihiko Asahina,Hidemi Nakagawa
标识
DOI:10.1111/1346-8138.13860
摘要
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.
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