Dermatologia, Dipartimento di Medicina e Chirurgia Traslazionale, Università Cattolica del Sacro Cuore, Rome, Italy.
Dermatologia, Dipartimento di Scienze Mediche e Chirurgiche, Fondazione Policlinico Universitario A. Gemelli-IRCCS, Rome, Italy.
J Dermatolog Treat. 2023 Dec;34(1):2230685. doi: 10.1080/09546634.2023.2230685.
The purpose of this study was to analyze the drug survival rate of dupilumab up to 2 years in a large real-world cohort of adult patients affected by moderate/severe atopic dermatitis (AD), and to investigate the clinical, demographic and predictive factors influencing the patients' treatment persistence.
This study included adult patients affected by moderate-to-severe AD treated with dupilumab for at least 16 weeks who visited 7 dermatologic outpatient clinics in Lazio, Italy, from January 2019 until August 2021.
A total of 659 adult patients (345 male [52.3%], mean age: 42.8 years) with an average treatment duration of 23.3 months were enrolled in the study. Overall, 88.6% and 76.1% of patients were still on treatment after 12 and 24 months, respectively. The drug survival rate for discontinuation due to AEs and dupilumab ineffectiveness was 95.0% at 12 months and 90.0% at 24 months. The main reasons for drug discontinuation included inefficacy (29.6%), failed compliance (17.4%), persistent efficacy (20.4%) and adverse events (7.8%). Adult AD onset (≥18 years) and EASI score severity measured at the last follow-up visit were the only factors significantly associated with lower drug survival.
This study revealed an increased cumulative probability of dupilumab survival at 2 years, reflected by a sustained effectiveness and a favorable safety profile of the drug.
本研究旨在分析达必妥治疗中重度特应性皮炎(AD)成人患者长达 2 年的药物生存率,并探讨影响患者治疗持续时间的临床、人口统计学和预测因素。
本研究纳入了自 2019 年 1 月至 2021 年 8 月在意大利拉齐奥地区 7 家皮肤科门诊接受至少 16 周达必妥治疗的中重度 AD 成年患者。
共纳入 659 名成年患者(345 名男性[52.3%],平均年龄:42.8 岁),平均治疗时间为 23.3 个月。总体而言,分别有 88.6%和 76.1%的患者在 12 个月和 24 个月时仍在接受治疗。因不良事件和达必妥无效而停药的药物生存率在 12 个月时为 95.0%,在 24 个月时为 90.0%。停药的主要原因包括无效(29.6%)、未能遵医嘱(17.4%)、持续有效(20.4%)和不良事件(7.8%)。成人 AD 发病(≥18 岁)和最后一次随访时 EASI 评分严重程度是与较低药物生存率显著相关的唯一因素。
本研究显示达必妥在 2 年时的累积生存率增加,反映了药物持续有效性和良好的安全性。