Assessing the Impact of Efalizumab on Nail, Scalp and Palmoplantar Psoriasis and on Quality of Life: Results from a Multicentre, Open-label, Phase IIIb/IV Trial.

Andreas Katsambas, Ketty Peris, Gino Vena, Peter Freidmann, Gottfried Wozel, Esteban Daudén, Daiana Licu, Mauro Placchi, Michel De La Brassinne
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引用次数: 15

Abstract

This post-approval, open-label trial (n = 1266) assessed the efficacy of efalizumab, administered in accordance with the European label at that time, in patients with concomitant nail, scalp or palmoplantar psoriasis. Patients received subcutaneous efalizumab 1.0 mg/kg weekly for up to 20 weeks. By Week 12, an improvement from baseline of 50% or more was observed in 21.4% (181/844) of patients with nail psoriasis, 62.4% (718/1150) of patients with scalp psoriasis, and 51.4% (127/247) of patients with palmoplantar psoriasis. Quality of life improved throughout the trial, with a 50% median improvement in DLQI score after 12 weeks of treatment. Efalizumab showed promising efficacy in the treatment of nail, scalp and palmoplantar psoriasis, which was reflected in improvements in quality of life.

Abstract Image

Abstract Image

评估Efalizumab对指甲、头皮和掌跖牛皮癣的影响以及对生活质量的影响:来自多中心、开放标签、iii /IV期试验的结果
这项批准后的开放标签试验(n = 1266)评估了依法利珠单抗在合并指甲、头皮或掌跖牛皮癣患者中的疗效,按照当时的欧洲标签给药。患者接受每周一次皮下法利珠单抗1.0 mg/kg治疗,持续20周。到第12周,21.4%(181/844)的甲型银屑病患者、62.4%(718/1150)的头皮型银屑病患者和51.4%(127/247)的掌型足底型银屑病患者较基线改善50%或以上。在整个试验过程中,生活质量得到了改善,治疗12周后DLQI评分中位数改善了50%。Efalizumab在治疗指甲、头皮和掌跖牛皮癣方面显示出良好的疗效,这反映在生活质量的改善上。
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