Engin Burhan, Demir Yusuf, Yucesoy Sera Nur, Ak Tumay
Department of Dermatology, Istanbul University-Cerrahpasa, Cerrahpasa Medical Faculty, Istanbul, Turkey.
Department of Dermatology, Istanbul University-Cerrahpasa, Cerrahpasa Medical Faculty, Istanbul, Turkey.
An Bras Dermatol. 2025 Jun 18;100(4):501132. doi: 10.1016/j.abd.2025.501132.
Psoriasis is a chronic multisystem disorder, and the inhibition of different cytokine pathways has been associated with different treatment responses.
To demonstrate independent predictors of PASI90 response in patients with psoriasis under biologic therapy and compare the effectiveness of different biologic classes METHODS: This cross-sectional study was conducted in a single tertiary center between January 2023 and May 2024 and included 623 patients (M/F: 320/303). PASI90 response was the primary end-point of the study, and PASI100 was the secondary end-point. Univariate and multivariate cox-regression analyses were used to identify predictors of PASI90. The efficacy of different biologic classes for achieving PASI90 and PASI100 responses was assessed using the Kaplan-Meier method.
The age of disease onset (HR = 1.037, 95% CI [1.029‒1.044], p < 0.001) and being biologic-naïve (HR = 1.261, 95% CI [1.046‒1.521], p = 0.015) were identified as significant predictors of PASI90 response. IL23 inhibitors showed considerably superior efficacy in achieving PASI90 response than both TNF inhibitors (p = 0.042) and ustekinumab (p = 0.027). Also, IL17 inhibitors exhibited near-significantly higher effectiveness than TNF inhibitors (p = 0.090) and ustekinumab (p = 0.050). The performance of biologic classes was not substantially different in reaching PASI100 overall.
The most important limitation of this study is the retrospective data collection.
Age of disease onset and being biologically naïve were positively associated with achieving PASI90 response, whereas ustekinumab use was negatively associated. Age of disease onset was the strongest predictor of PASI90. Also, IL23 and IL17 inhibition, especially IL23, appeared to provide a better therapeutic response.
银屑病是一种慢性多系统疾病,不同细胞因子通路的抑制与不同的治疗反应相关。
证明接受生物治疗的银屑病患者达到PASI90反应的独立预测因素,并比较不同生物制剂类别的疗效。
这项横断面研究于2023年1月至2024年5月在一家单一的三级中心进行,纳入623例患者(男/女:320/303)。PASI90反应是研究的主要终点,PASI100是次要终点。采用单因素和多因素cox回归分析来确定PASI90的预测因素。使用Kaplan-Meier方法评估不同生物制剂类别实现PASI90和PASI100反应的疗效。
发病年龄(HR = 1.037,95%CI [1.029‒1.044],p < 0.001)和初用生物制剂(HR = 1.261,95%CI [1.046‒1.521],p = 0.015)被确定为PASI90反应的显著预测因素。IL23抑制剂在实现PASI90反应方面显示出比TNF抑制剂(p = 0.042)和优特克单抗(p = 0.027)显著更高的疗效。此外,IL17抑制剂显示出比TNF抑制剂(p = 0.090)和优特克单抗(p = 0.050)略高的有效性。不同生物制剂类别在总体达到PASI100方面的表现没有实质性差异。
本研究最重要的局限性是回顾性数据收集。
发病年龄和初用生物制剂与实现PASI90反应呈正相关,而使用优特克单抗则呈负相关。发病年龄是PASI90最强的预测因素。此外,抑制IL23和IL17,尤其是IL23,似乎能提供更好的治疗反应。