TNF-alpha inhibitors and ustekinumab for the treatment of psoriasis: therapeutic utility in the era of IL-17 and IL-23 inhibitors.

Q3 Medicine
Julie J Hong, Edward K Hadeler, Megan L Mosca, Nicholas D Brownstone, Tina Bhutani, Wilson J Liao
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引用次数: 0

Abstract

Psoriasis is a chronic inflammatory condition for which eleven FDA-approved biologic therapies are approved. Over the past decade, studies have documented the higher efficacy of IL-17 and IL-23 inhibitors for the treatment of psoriasis compared to the TNF-alpha inhibitors and ustekinumab, an IL-12/23 inhibitor. Despite this, there remains an important role for the use of TNF-alpha inhibitors and ustekinumab in the treatment of psoriasis. Here, we review how considerations of infection and malignancy risk, patient demographics, treatment resistance, and co-morbidities may make certain TNF-alpha inhibitors or ustekinumab an excellent choice for therapy in particular patient subgroups.

治疗银屑病的 TNF-α 抑制剂和乌司他单抗:IL-17 和 IL-23 抑制剂时代的治疗效用。
银屑病是一种慢性炎症性疾病,美国食品和药物管理局已批准了 11 种生物疗法。在过去十年中,有研究表明,与TNF-α抑制剂和IL-12/23抑制剂ustekinumab相比,IL-17和IL-23抑制剂治疗银屑病的疗效更高。尽管如此,TNF-α抑制剂和乌斯特库单抗在银屑病治疗中仍然发挥着重要作用。在此,我们回顾了感染和恶性肿瘤风险、患者人口统计学、治疗耐药性和合并症等因素如何使某些 TNF-α 抑制剂或乌斯特库单抗成为特定患者亚群治疗的最佳选择。
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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来源期刊
CiteScore
1.30
自引率
0.00%
发文量
19
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