Seneschal J, Lacour J-P, Bewley A, Faurby M, Paul C, Pellacani G, De Simone C, Horne L, Sohrt A, Augustin M, Hammond E, Reich K
Department of Dermatology and Paediatric Dermatology, National Reference Centre for Rare Skin Diseases, Saint-André Hospital, University of Bordeaux, Bordeaux, France.
Department of Dermatology, Archet 2 Hospital, University Hospital of Nice, Nice, France.
J Eur Acad Dermatol Venereol. 2020 Nov;34(11):2566-2573. doi: 10.1111/jdv.16568. Epub 2020 Jun 8.
Anti-tumour necrosis factor (TNF) and anti-interleukin (IL)-12/23 biologics revolutionized plaque psoriasis treatment by enabling ≥75% improvement in the Psoriasis Area and Severity Index (PASI 75) in clinical trials. Modern biologics are now reported to achieve PASI 100 (complete skin clearance) in clinical trials. However, real-world evidence of skin clearance rates with biologics is limited. PSO-BIO-REAL was conducted to understand the real-world burden of plaque psoriasis.
The primary objective of this observational study was to estimate the proportion of patients who achieved complete skin clearance at 6 months. Secondary objectives included maintenance of response and evaluation of complete skin clearance at 12 months.
PSO-BIO-REAL was a multinational, prospective, real-world, non-interventional study of skin clearance and patient-reported outcomes (PROs) with biologics. A total of 846 patients from the United States (32%), France (28%), Italy (22%), the United Kingdom (11%) and Germany (8%) were enrolled and followed for one year. Eligible patients were aged ≥18 years with moderate-to-severe plaque psoriasis who had initiated a biologic for plaque psoriasis. Patients could be biologic-naïve or switching biologics (biologic-experienced). Assessments were made at baseline and at months 6 and 12.
At 6 and 12 months, 23% and 26% of patients achieved complete skin clearance, respectively. Prior to study entry, 60% were biologic-naïve. The proportion of patients achieving complete skin clearance was lower among biologic-experienced patients (20% at both months 6 and 12) compared with biologic-naïve patients (25% at month 6, 30% at month 12). The rate of complete skin clearance decreased as the number of prior biologics and baseline comorbidities increased.
Only one in four patients achieved complete skin clearance after 6 months of treatment with biologics. The study indicates there still is an unmet need for more efficacious biologics for patients with psoriasis.
抗肿瘤坏死因子(TNF)和抗白细胞介素(IL)-12/23生物制剂在临床试验中使银屑病面积和严重程度指数(PASI 75)改善率≥75%,从而彻底改变了斑块状银屑病的治疗方式。据报道,现代生物制剂在临床试验中可实现PASI 100(皮肤完全清除)。然而,生物制剂实现皮肤清除率的真实世界证据有限。开展PSO-BIO-REAL研究旨在了解斑块状银屑病的真实世界负担。
这项观察性研究的主要目的是估计在6个月时实现皮肤完全清除的患者比例。次要目的包括维持反应以及评估12个月时的皮肤完全清除情况。
PSO-BIO-REAL是一项针对生物制剂的皮肤清除率和患者报告结局(PROs)的跨国、前瞻性、真实世界、非干预性研究。共纳入来自美国(32%)、法国(28%)、意大利(22%)、英国(11%)和德国(8%)的846例患者,并随访一年。符合条件的患者年龄≥18岁,患有中度至重度斑块状银屑病,且已开始使用生物制剂治疗斑块状银屑病。患者可以是初用生物制剂者或正在转换生物制剂(有生物制剂使用经验者)。在基线以及第6个月和第12个月进行评估。
在第6个月和第12个月时,分别有23%和26%的患者实现了皮肤完全清除。在研究入组前,60%为初用生物制剂者。与初用生物制剂者(第6个月时为25%,第12个月时为30%)相比,有生物制剂使用经验的患者实现皮肤完全清除的比例较低(第6个月和第12个月时均为20%)。随着既往生物制剂使用次数和基线合并症数量的增加,皮肤完全清除率降低。
使用生物制剂治疗6个月后,只有四分之一的患者实现了皮肤完全清除。该研究表明,对于银屑病患者而言,对更有效的生物制剂仍有未满足的需求。