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口服阿维A酯联合卡泊三醇乳膏与单用阿维A酯治疗中重度银屑病的疗效和安全性临床试验

Clinical trial of the efficacy and safety of oral etretinate with calcipotriol cream compared with etretinate alone in moderate-severe psoriasis.

作者信息

Giannetti A, Coppini M, Bertazzoni M G, Califano A, Altieri E, Pazzaglia A, Lega M, Lombardo M, Pelfini C, Veller Fornasa C, Rabbiosi G, Cespa M

机构信息

Clinica Dermatologica, Università, Modena, Italy.

出版信息

J Eur Acad Dermatol Venereol. 1999 Sep;13(2):91-5.

Abstract

BACKGROUND

The aim of this clinical trial was to assess the efficacy and safety of calcipotriol cream associated with oral etretinate compared with etretinate alone in the treatment of moderate-severe psoriasis.

METHODS

This controlled multicenter trial, within patients (hemiparts), enrolled 86 in- or out-patients (62 males, 24 females), mean (+/-SD) age 57.1 +/- 14.2 years, with psoriasis vulgaris on both sides of the body, and mean (+/-SE) baseline PASI score (Psoriasis Area and Severity Index) 30.7 +/- 0.9. All patients took oral etretinate 50 mg/day and applied calcipotriol cream (50 microg/g) on one half of their body twice a day. Treatment was continued for 9 weeks, and patients were seen every 3 weeks.

RESULTS

At the end of the first 3 weeks the PASI score indicated a significant clinical difference between the two sides of the body (P < 0.001, ANOVA), with a reduction of 50.7% in the score for the calcipotriol-treated half, compared with a 39% reduction for the untreated half. By the 9th week of treatment the PASI score was 81.4% lower on the treated half, and 70.3% on the untreated side (P < 0.001, ANOVA).

CONCLUSIONS

These findings suggest that patients with moderate-severe psoriasis might benefit from treatment with etretinate plus calcipotriol, with the aim of achieving a faster response and an overall smaller total dose of etretinate.

摘要

背景

本临床试验的目的是评估卡泊三醇乳膏联合口服依曲替酯与单用依曲替酯治疗中重度银屑病的疗效和安全性。

方法

本对照多中心试验纳入了86例门诊或住院患者(半身),其中男性62例,女性24例,平均(±标准差)年龄57.1±14.2岁,全身双侧患有寻常型银屑病,平均(±标准误)基线银屑病面积和严重程度指数(PASI)评分为30.7±0.9。所有患者每日口服依曲替酯50mg,并在身体一侧每日两次涂抹卡泊三醇乳膏(50μg/g)。治疗持续9周,每3周对患者进行一次检查。

结果

在最初3周结束时,PASI评分显示身体两侧存在显著临床差异(P<0.001,方差分析),卡泊三醇治疗侧的评分降低了50.7%,而未治疗侧降低了39%。到治疗第9周时,治疗侧的PASI评分降低了81.4%,未治疗侧降低了70.3%(P<0.001,方差分析)。

结论

这些结果表明,中重度银屑病患者可能从依曲替酯加卡泊三醇的治疗中获益,目的是实现更快的反应并总体减少依曲替酯的总剂量。

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