U.O.C. di Dermatologia, Dipartimento Scienze Mediche e Chirurgiche, Fondazione Policlinico Universitario A. Gemelli IRCCS, Rome, Italy.
Dermatologia, Dipartimento Universitario di Medicina e Chirurgia Traslazionale, Università Cattolica del Sacro Cuore, Rome, Italy.
J Dermatolog Treat. 2023 Dec;34(1):2246606. doi: 10.1080/09546634.2023.2246606.
Ixekizumab is a high-affinity monoclonal antibody that selectively targets interleukin (IL)-17A approved for the treatment of moderate-to-severe plaque psoriasis. The objective of this study was to describe the real-world long-term effectiveness of ixekizumab in patients with plaque psoriasis in Italy.
A retrospective study was conducted in patients affected by moderate-to-severe plaque psoriasis who were continuously treated with ixekizumab for at least 12 months. Patient data was obtained at 4-weeks, 12-weeks and 6-, 12-, 18- and 24-months after baseline (June 2017 and September 2019) from 10 sites. Results were analyzed by complete case approach, with sensitivity analysis performed to evaluate the impact of missing data.
A total of 198 patients were enrolled in the study. At Month 24, 94.3% of patients achieved PASI75 response, while 85.1 and 71.8% achieved PASI90 and PASI100, respectively; and 91.1% of the patients achieved absolute PASI score ≤2. Patients experienced psoriasis improvement at 4 weeks after starting treatment, and improvement was maintained with continued ixekizumab use. The quality of life of patients also improved significantly starting at Week 12, with sustained effect in the long term.
This 24-month observational cohort study confirmed that ixekizumab is effective in the long-term management of patients with moderate-to-severe plaque psoriasis.
依奇珠单抗是一种高亲和力的单克隆抗体,选择性靶向白细胞介素(IL)-17A,已被批准用于治疗中度至重度斑块型银屑病。本研究的目的是描述依奇珠单抗在意大利斑块型银屑病患者中的真实世界长期疗效。
对至少连续接受依奇珠单抗治疗 12 个月的中度至重度斑块型银屑病患者进行回顾性研究。从 10 个地点获得患者在基线(2017 年 6 月和 2019 年 9 月)后 4 周、12 周、6 个月、12 个月、18 个月和 24 个月的数据。采用全分析集方法进行分析,并进行敏感性分析以评估缺失数据的影响。
共有 198 名患者入组研究。在第 24 个月时,94.3%的患者达到 PASI75 缓解,85.1%和 71.8%的患者分别达到 PASI90 和 PASI100 缓解,91.1%的患者达到绝对 PASI 评分≤2。患者在开始治疗后 4 周开始出现银屑病改善,且随着依奇珠单抗的持续使用,改善得以维持。患者的生活质量也从第 12 周开始显著改善,并在长期内保持持续效果。
这项为期 24 个月的观察性队列研究证实,依奇珠单抗在中度至重度斑块型银屑病患者的长期管理中是有效的。