腿部受累的银屑病成为新的治疗难点:利桑珠单抗治疗患者的队列研究。

IF 2.5 4区 医学 Q2 DERMATOLOGY Dermatology practical & conceptual Pub Date : 2024-07-01 DOI:10.5826/dpc.1403a171
Federico Bardazzi, Federica Filippi, Martina Mussi, Claudia Lasagni, Laura Bigi, Giulia Odorici, Francesca Peccerillo, Miriam Rovesti, Francesca Satolli, Michela Tabanelli, Sandra Schianchi, Vito Di Lernia, Marco Manfredini
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引用次数: 0

摘要

简介:一直以来,银屑病的难治部位包括面部、头皮、皱褶、生殖器、指甲和掌跖。最近的研究发现,下肢是 "新 "的难治部位,因为即使是接受生物疗法的患者,下肢也可能是唯一有残余疾病的部位:我们的目的是评估与身体其他部位相比,腿部对新型生物药物利桑珠单抗治疗的反应率和反应时间是否有所不同:我们进行了一项真实的、观察性的、回顾性的多中心研究,研究对象包括腿部受累的中重度银屑病患者,他们接受利坦珠单抗生物治疗的时间超过16周。在T0和第16、28、40、52、64和76周时收集了银屑病面积严重程度指数(PASI)和腿部PASI。统计分析采用学生 t 检验和线性回归分析:结果:共纳入 124 名患者。与基线相比,第 16 周和第 28 周的改善百分比差异具有统计学意义,这表明腿部-PASI 的改善程度低于 PASI。从线性回归中可以推断出,腿部PASI的斜率在统计学上没有整体PASI那么陡峭,这证实了该部位对治疗的反应更慢:结论:在治疗的最初几周,腿部对利桑单抗的反应似乎与身体其他部位有明显不同,即使在治疗 28 周后,统计意义已经消失。我们的初步研究结果表明,利桑珠单抗可被视为治疗腿部银屑病的有效药物,但与其他部位相比,利桑珠单抗的反应时间更长,这表明该部位的抗药性具有相对性。
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Psoriasis with Leg Involvement as the New Difficult-To-Treat Area: A Cohort Study of Patients Treated With Risankizumab.

Introduction: Historically, difficult-to-treat areas in psoriasis included face, scalp, folds, genitalia, nails, and palmoplantar region. Recent studies have found that lower limbs behave like a "new" difficult-to-treat area as they can be the only site of residual disease even in patients undergoing biologic therapies.

Objectives: We aimed to evaluate whether legs had different response rates and response times to treatment with a new biologic drug, risankizumab, compared to other body sites.

Methods: We conducted a real-life, observational, retrospective, multicenter study including patients affected by moderate-to-severe psoriasis with leg involvement and undergoing biological therapy with risankizumab for more than 16 weeks. The Psoriasis Area Severity Index (PASI) and Leg-PASI were collected at T0 and at weeks 16, 28, 40, 52, 64, and 76. Statistical analysis using Student's t test and linear regression analysis were performed.

Results: A total of 124 patients were included. The difference between the improvement percentage compared to baseline was statistically significant at weeks 16 and 28, demonstrating that Leg-PASI improved less than PASI. From the linear regression it was deduced that the slope is statistically less steep for Leg-PASI than for overall PASI, confirming that this site responds more slowly to the therapy.

Conclusions: Leg response to risankizumab appears to differ significantly from other body sites in the first weeks of treatment, even if after 28 weeks, statistical significance is lost. Our preliminary finding suggests that risankizumab can be considered an effective treatment for leg psoriasis but with longer response times than other areas, demonstrating the relative nature of resistance to treatment of this district.

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