Yıldırım Fatma Elif, Hapa Fatma Aslı
Department of Dermatology, Faculty of Medicine, Sanko University, Gaziantep, Turkey.
Dermatology Clinic, Democracy University, Buca Seyfi Demirsoy Training and Research Hospital, Izmir, Turkey.
Postepy Dermatol Alergol. 2024 Feb;41(1):49-55. doi: 10.5114/ada.2023.135757. Epub 2024 Feb 28.
Secukinumab (SEC) has been shown to be highly effective and safe in the treatment of moderate to severe plaque psoriasis (PsO), but data on SEC's long-term drug survival are limited.
To analyse the survival rate of SEC and its predictive factors of survival, together with the drug safety and efficacy.
Data of 268 patients who received SEC between May 2018 and April 2022 with moderate to severe psoriasis and/or psoriatic arthritis were analysed retrospectively. Psoriasis Area Severity Index (PASI) was used to define effectiveness. Drug survival was examined using the Kaplan-Meier analysis and Cox regression analysis was used to analyse predictive factors.
PASI 75/90/100 responses achieved at week 16 (89.5%, 78%, and 16.2%, respectively) were well maintained at week 52 (96.3%, 90.7%, and 15.4%, respectively). The drug survival probability rates for SEC were 94.4% at 12 months, 88.4% at 24 months, 78.6% after 3 years, 52.7% after 4 years. Concomitant treatments, dose escalation and family history of psoriasis were associated with a higher risk for SEC withdrawal.
Close monitoring may improve SEC survival in psoriasis patients who require dose escalation and concomitant drugs.
司库奇尤单抗(SEC)已被证明在治疗中度至重度斑块状银屑病(PsO)方面具有高效性和安全性,但关于SEC长期药物留存率的数据有限。
分析SEC的留存率及其留存的预测因素,以及药物的安全性和有效性。
回顾性分析2018年5月至2022年4月期间接受SEC治疗的268例中度至重度银屑病和/或银屑病关节炎患者的数据。采用银屑病面积和严重程度指数(PASI)来定义疗效。使用Kaplan-Meier分析检查药物留存情况,并使用Cox回归分析来分析预测因素。
在第16周达到的PASI 75/90/100缓解率(分别为89.5%、78%和16.2%)在第52周时得到了很好的维持(分别为96.3%、90.7%和15.4%)。SEC的药物留存概率在12个月时为94.4%,24个月时为88.4%,3年后为78.6%,4年后为52.7%。联合治疗、剂量增加和银屑病家族史与更高的SEC停药风险相关。
对于需要增加剂量和联合用药的银屑病患者,密切监测可能会提高SEC的留存率。