Department of Dermatology, Shanghai Tenth People's Hospital, Tongji University School of Medicine, Shanghai, 200072, China.
Clin Drug Investig. 2018 Mar;38(3):191-199. doi: 10.1007/s40261-017-0603-3.
Psoriasis is an immune-mediated polygenic inherited skin disease. Many biologic agents have been approved for the treatment of moderate-to-severe plaque psoriasis. The most commonly utilized biologics include TNF-α antagonists (etanercept, infliximab, and adalimumab), IL-12/23P40 antagonist (ustekinumab), IL-23P19 antagonist (guselkumab), IL-17A antagonist (secukinumab and ixekizumab), and IL-17RA antagonist (brodalumab). However, some patients may fail to respond well to their first biologic agent. Reasons for failure include primary failure (lack of initial efficacy), secondary failure (loss of efficacy over time) or the development of adverse effects. For patients desiring maximum skin clearance and better quality of life, switching to a second biologic agent might be a worthwhile option. This review discusses recent clinical studies on switching therapies in treating psoriasis, and found that switching biologic agents can significantly improve outcomes for patients. Some clinical guidelines are also discussed. This research provides some advice on establishing individualized treatment regimens based on clinical needs and pharmacologic characteristics.
银屑病是一种免疫介导的多基因遗传性皮肤疾病。许多生物制剂已被批准用于治疗中重度斑块状银屑病。最常用的生物制剂包括 TNF-α 拮抗剂(依那西普、英夫利昔单抗和阿达木单抗)、IL-12/23P40 拮抗剂(乌司奴单抗)、IL-23P19 拮抗剂(古塞库单抗)、IL-17A 拮抗剂(司库奇尤单抗和依奇珠单抗)和 IL-17RA 拮抗剂(布罗达单抗)。然而,一些患者可能对他们的第一种生物制剂反应不佳。失败的原因包括原发性失败(缺乏初始疗效)、继发性失败(随着时间的推移疗效丧失)或不良反应的发生。对于渴望获得最大皮肤清除率和更高生活质量的患者,切换至第二种生物制剂可能是一个值得的选择。本文综述了最近关于银屑病治疗中转换治疗的临床研究,发现转换生物制剂可以显著改善患者的疗效。还讨论了一些临床指南。本研究为根据临床需求和药物特性制定个体化治疗方案提供了一些建议。