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环孢素低剂量联合卡泊三醇/倍他米松二丙酸酯软膏治疗中重度斑块状银屑病:一项随机对照开放性研究。

Combined treatment with low-dose cyclosporine and calcipotriol/betamethasone dipropionate ointment for moderate-to-severe plaque psoriasis: a randomized controlled open-label study.

机构信息

2nd Dermatology Clinic, University of Bari, Bari, Italy.

出版信息

J Dermatolog Treat. 2012 Aug;23(4):255-60. doi: 10.3109/09546634.2011.565017. Epub 2011 Jul 14.

DOI:10.3109/09546634.2011.565017
PMID:21756153
Abstract

Combination therapy is a common approach to psoriasis, aimed at improving clinical response and minimizing the risk of side effects. The aim of this pilot randomized open-label study was to evaluate the efficacy and safety of the combination of low-dose cyclosporine (CsA) with calcipotriol-betamethasone dipropionate (CBD) ointment in the treatment of psoriasis. Sixty patients with moderate-to-severe plaque psoriasis were randomized to receive CsA, 2 mg/kg/day, combined with CBD ointment (n = 30) or CsA, at the same daily dosage, in combination with an emollient (n = 30), for 8 weeks. The primary efficacy parameter was the Psoriasis Area and Severity Index (PASI) 75 response rate at 8 weeks. Combination therapy with CsA and CBD ointment was more effective than CsA and emollient treatment, with statistically significant results, particularly less itching after 4 and 8 weeks and PASI reduction at all post-baseline visits. Significantly more patients treated with CsA + CBD achieved the PASI 75 at 8th week (87% vs 37% in the CsA-emollient group; p = 0.0001). The efficacy results were paralleled by the investigator and patient's global assessment of disease severity at the end of study. Our results suggest that the addition of CBD ointment to low-dose CsA enhances clinical response and improves the risk/benefit ratio.

摘要

联合治疗是治疗银屑病的常用方法,旨在提高临床疗效并降低不良反应风险。本研究旨在评估低剂量环孢素(CsA)联合卡泊三醇-倍他米松二丙酸酯(CBD)软膏治疗银屑病的疗效和安全性。

将 60 例中重度斑块状银屑病患者随机分为两组,分别接受低剂量 CsA(2mg/kg/天)联合 CBD 软膏(n=30)或 CsA 联合保湿剂(n=30)治疗 8 周。主要疗效参数为 8 周时的银屑病面积和严重程度指数(PASI)75 缓解率。

结果表明,与 CsA 联合保湿剂相比,CsA 联合 CBD 软膏治疗更有效,具有统计学意义,特别是在第 4 周和第 8 周时瘙痒减轻,在所有随访时 PASI 评分降低。在第 8 周时,更多接受 CsA+CBD 治疗的患者达到 PASI 75(87%比 CsA+保湿剂组的 37%;p=0.0001)。疗效结果与研究结束时研究者和患者对疾病严重程度的全球评估一致。

这些结果表明,在低剂量 CsA 中加入 CBD 软膏可增强临床疗效,提高风险/获益比。

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