Hagino Teppei, Onda Marina, Saeki Hidehisa, Fujimoto Eita, Kanda Naoko
Department of Dermatology, Nippon Medical School Chiba Hokusoh Hospital, Inzai, Japan.
Department of Dermatology, Nippon Medical School, Tokyo, Japan.
J Dermatol. 2025 Mar;52(3):551-555. doi: 10.1111/1346-8138.17601. Epub 2024 Dec 26.
The tyrosine kinase 2 inhibitor deucravacitinib is therapeutically effective for psoriasis. However, predictive factors for high responses to deucravacitinib have not been examined in a real-world clinical study. Our study aimed to identify predictive factors for responders to deucravacitinib. Therefore, a retrospective study was conducted on 74 patients with psoriasis treated with deucravacitinib (6 mg/day) at week 16 of treatment from January 2023 to February 2024. Patients were classified into responders (achievers of a static Physician's Global Assessment [sPGA] of 0 or 1 with ≥2-point improvement from basal sPGA) and non-responders (non-achievers). We compared baseline values of clinical and laboratory indexes between responders and non-responders. Multivariate logistic regression analysis was used to identify variables predicting responders. Forty-one patients (55.4%) were considered as responders at week 16. Multivariate logistic regression analysis revealed that the response to deucravacitinib was associated with higher age (odds ratio [OR] 1.04; 95% confidence interval [CI] 1.01-1.08; p = 0.0222) and lower body mass index (BMI) (OR 0.825; 95% CI 0.713-0.955; p = 0.0101). Higher age and lower BMI may predict a higher response to deucravacitinib (6 mg/day) at week 16 of treatment.
酪氨酸激酶2抑制剂氘可来昔替尼对银屑病具有治疗效果。然而,在真实世界临床研究中尚未对氘可来昔替尼高反应性的预测因素进行研究。我们的研究旨在确定氘可来昔替尼反应者的预测因素。因此,对2023年1月至2024年2月期间接受氘可来昔替尼(6毫克/天)治疗16周的74例银屑病患者进行了一项回顾性研究。患者被分为反应者(静态医师整体评估[sPGA]为0或1且较基线sPGA改善≥2分者)和无反应者(未达到上述标准者)。我们比较了反应者和无反应者临床及实验室指标的基线值。采用多因素logistic回归分析来确定预测反应者的变量。41例患者(55.4%)在第16周被视为反应者。多因素logistic回归分析显示,对氘可来昔替尼的反应与较高年龄(比值比[OR]1.04;95%置信区间[CI]1.01 - 1.08;p = 0.0222)和较低体重指数(BMI)(OR 0.825;95%CI 0.713 - 0.955;p = 0.0101)相关。较高年龄和较低BMI可能预测治疗第16周时对氘可来昔替尼(6毫克/天)有更高反应。