首页> 美国卫生研究院文献>The Journal of Clinical and Aesthetic Dermatology >A Preliminary Open Label Single-arm Study of Calcipotriene/Betamethasone Topical Suspension as a Supplement to Non-biologic Systemic Therapy for Psoriasis
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A Preliminary Open Label Single-arm Study of Calcipotriene/Betamethasone Topical Suspension as a Supplement to Non-biologic Systemic Therapy for Psoriasis

机译:初步的开放标签的单臂研究卡泊三烯/倍他米松局部悬浮液作为牛皮癣非生物系统疗法的补充

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摘要

>Background: Calcipotriene/betamethasone topical suspension is a topical therapy that is often used as monotherapy as a first-line treatment for plaque psoriasis. The objective of this preliminary, open label, single arm study was to determine the efficacy of adding a topical suspension to a traditional systemic therapy for psoriasis, either methotrexate or acitretin. >Methods: In this exploratory study, eight patients with chronic plaque psoriasis who were on stable methotrexate or acitretin treatment without clearance were treated with once-daily calcipotriene/betamethasone topical suspension. Subjects completed five study visits over 12 weeks. Primary outcome measure was improvement of two or more points in Investigator Global Assessment. Secondary endpoints included change in Body Surface Area, Dermatology Life Quality Index, and Patient’s Global Assessment from baseline to Week 12. >Results: Overall, the median decrease in Investigator Global Assessment over 12 weeks was 1.5 points, with 50 percent of subjects experiencing a drop of two or more points in Investigator Global Assessment. All eight subjects had a reduction in Body Surface Area and Patient’s Global Assessment. There was a mean decrease in Dermatology Life Quality Index score of 78.9 percent, showing improved patient quality of life. In addition, all patients tolerated the treatment well and 6 of 8 patients had improved satisfaction level with their treatment by the end of the study. >Conclusion: The topical suspension was effective and well-tolerated in conjunction with stable methotrexate or acitretin treatment in all eight patients in this study. These results support the feasibility of a larger scale study to further investigate the efficacy of these treatment combinations. The trial is registered at ClinicalTrials.gov, number .
机译:>背景:卡泊三烯/倍他米松局部混悬液是一种局部疗法,通常作为单一疗法用作斑块状牛皮癣的一线治疗。这项初步的,开放标签的单臂研究的目的是确定在传统的全身性牛皮癣银屑病或甲氨蝶呤疗法中添加局部混悬液的疗效。 >方法:在这项探索性研究中,每天用一次卡泊三烯/倍他米松局部混悬液治疗8例接受稳定氨甲蝶呤或阿维A酸治疗但未清除的慢性斑块状牛皮癣患者。受试者在12周内完成了5次研究访问。主要结果指标是调查者全球评估中的两个或更多点的改善。次要终点包括从基线到第12周的身体表面积,皮肤病生活质量指数和患者的总体评估的变化。>结果:总体而言,过去12周内研究者总体评估的中位数下降了1.5分,其中50%的受试者在调查者全球评估中得分下降两个或更多分。所有八名受试者的体表面积和患者总体评估均下降。皮肤病生活质量指数得分平均下降78.9%,表明患者的生活质量得到改善。此外,所有患者对治疗的耐受性良好,到研究结束时8例患者中有6例对治疗的满意度提高了。 >结论:在本研究中,所有八名患者的局部混悬液与稳定的甲氨蝶呤或阿维A净联合治疗均有效且耐受性良好。这些结果支持进行大规模研究以进一步研究这些治疗组合的功效的可行性。该试验已在ClinicalTrials.gov上注册,编号为。

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