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一项多国前瞻性观察性研究,旨在评估在真实世界环境中接受生物制剂治疗的中度至重度斑块状银屑病患者的完全皮肤清除情况(PSO-BIO-REAL)。

A multinational, prospective, observational study to estimate complete skin clearance in patients with moderate-to-severe plaque PSOriasis treated with BIOlogics in a REAL world setting (PSO-BIO-REAL).

作者信息

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

机构信息

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.

出版信息

J Eur Acad Dermatol Venereol. 2020 Nov;34(11):2566-2573. doi: 10.1111/jdv.16568. Epub 2020 Jun 8.

Abstract

BACKGROUND

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.

OBJECTIVE

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.

METHODS

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.

RESULTS

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.

CONCLUSION

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.

摘要

背景

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。

目的

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。

方法

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。

结果

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。

结论

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7977/7818467/359b28cac227/JDV-34-2566-g001.jpg

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