Secukinumab in the treatment of psoriasis: patient selection and perspectives.

IF 5.2 Q1 DERMATOLOGY
Psoriasis (Auckland, N.Z.) Pub Date : 2018-10-17 eCollection Date: 2018-01-01 DOI:10.2147/PTT.S146004
Eric J Yang, Kristen M Beck, Wilson Liao
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引用次数: 23

Abstract

Secukinumab is a human monoclonal antibody targeting IL-17A that has been approved for three indications: moderate-to-severe plaque psoriasis, psoriatic arthritis, and ankylosing spondylitis. In Phase III clinical trials for each of these three indications, secukinumab has proven to be both highly efficacious and well-tolerated. However, several biologic medications are currently approved for the treatment of moderate-to-severe plaque psoriasis, and many demonstrate excellent efficacy and safety. Due to this wide selection, it is often unclear how to choose biologics for specific patients. Important considerations in biologic selection include clinical efficacy, safety, cost, convenience, onset of action, and management of comorbid disease. This article aims to outline the key considerations in patient selection for the treatment of plaque psoriasis with secukinumab.

Secukinumab治疗牛皮癣:患者选择和观点。
Secukinumab是一种靶向IL-17A的人单克隆抗体,已被批准用于三种适应症:中度至重度斑块性银屑病、银屑病关节炎和强直性脊柱炎。在这三种适应症的III期临床试验中,secukinumab已被证明既高效又耐受性良好。然而,目前有几种生物药物被批准用于治疗中重度斑块性银屑病,并且许多药物显示出出色的疗效和安全性。由于这种广泛的选择,通常不清楚如何为特定患者选择生物制剂。生物制剂选择的重要考虑因素包括临床疗效、安全性、成本、便利性、起效和合并症的管理。本文旨在概述用secukinumab治疗斑块型银屑病患者选择时的关键考虑因素。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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