Benucci Maurizio, Damiani Arianna, Li Gobbi Francesca, Grossi Valentina, Infantino Maria, Manfredi Mariangela, Niccoli Laura, Cantini Fabrizio
Rheumatology Unit, Hospital S. Giovanni di Dio, Azienda USL-Toscana Centro, Florence, Italy.
Rheumatology Unit, University of Florence, Florence, Italy.
Ther Clin Risk Manag. 2020 Apr 16;16:287-297. doi: 10.2147/TCRM.S228880. eCollection 2020.
Over the last 20 years, the greatly improved knowledges of underlying pathogenic mechanisms of AS, including the role of tumor necrosis factor (TNF), the interleukin 23/Th17 axis, and interleukin-17 (Il-17), constituted the rationale to develop biologics selectively inhibiting these pathways. For more than 10 years, anti-TNF biologics were successfully employed to treat AS, with marked improvement of signs and symptoms in around 60% of the patients. Recent knowledge of the pathophysiology of spondyloarthritis has highlighted the emerging role of the IL-17/IL-23 axis. New therapies with selective biological drugs have emerged in the treatment of this pathology. In this review, we evaluated the effects of ixekizumab, a new anti-IL-17A, that was licensed both by EMA and FDA in August 2019 for the treatment of ankylosing spondylitis. The review highlights the efficacy and safety data of the 3 randomized controlled trials (COAST V-COAST W-COAST X) and those of the extension to 52 weeks of COAST V and COAST W.
在过去20年里,人们对强直性脊柱炎(AS)潜在致病机制的认识有了很大提高,包括肿瘤坏死因子(TNF)、白细胞介素23/辅助性T细胞17(Th17)轴以及白细胞介素-17(Il-17)的作用,这为开发选择性抑制这些途径的生物制剂提供了理论依据。十多年来,抗TNF生物制剂成功用于治疗AS,约60%的患者体征和症状有显著改善。最近对脊柱关节炎病理生理学的认识突出了白细胞介素-17/白细胞介素-23轴的新作用。针对这一病症的治疗出现了选择性生物药物的新疗法。在本综述中,我们评估了新型抗白细胞介素-17A药物ixekizumab的疗效,该药物于2019年8月获得欧洲药品管理局(EMA)和美国食品药品监督管理局(FDA)批准用于治疗强直性脊柱炎。本综述重点介绍了3项随机对照试验(COAST V、COAST W、COAST X)以及COAST V和COAST W延长至52周的疗效和安全性数据。