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卡泊三醇/倍他米松二丙酸酯复方凝胶治疗成人轻中度银屑病的疗效:一项 IV 期、多中心、随机、对照、前瞻性研究的盲法中期分析。

Efficacy of a fixed combination of calcipotriol/betamethasone dipropionate topical gel in adult patients with mild to moderate psoriasis: blinded interim analysis of a phase IV, multicenter, randomized, controlled, prospective study.

机构信息

Dermatologikum Hamburg, Hamburg, Germany.

SCIderm GmbH, Hamburg, Germany.

出版信息

J Eur Acad Dermatol Venereol. 2015 Jun;29(6):1156-63. doi: 10.1111/jdv.12774. Epub 2014 Oct 26.

Abstract

BACKGROUND

Psoriasis is a common, chronic, inflammatory skin disease with the majority of individuals having limited disease, treated with topical medication. However, special attributes of topical treatments like galenic/cosmetic properties or an inconvenient treatment schedule may result in low preference for topical treatments. Hence, there is strong medical need for a topical medication, which is highly efficacious, easy-to-use and preferred by both physicians and patients.

OBJECTIVE

Blinded interim analysis with the purpose to assess efficacy of (both from the physician's and patient's perspective) and the patients' preference with a highly efficacious and easy-to-use fixed combination of calcipotriol/betamethasone dipropionate topical gel after 8 weeks of once daily treatment in a large patient population.

METHODS

In this phase IV, international, multicentre, randomized, controlled, prospective, parallel group study, adult patients with active, mild to moderate psoriasis despite previous topical psoriasis treatment, i.e. unsuccessful in the 8 weeks preceding study participation, are followed over 64 weeks. During the first 8 weeks the patients apply their medication once a day followed by a 56-weeks maintenance period according to SmPC. Blinded interim analysis of all patients included demographics, Physician's Global Assessment, the novel Patient's self Global Assessment (PsGA) and Patient Preference Questionnaire (PPQ).

RESULTS

1795 patients were analysed. At week 8, 36.5% of the physicians rated the patients' psoriasis as clear/almost clear. Similarly, based on the patients' self-assessment, 34.2% had a clear/almost clear score of PsGA in week 8. Analysis of the PPQ showed that the vast majority of the patients judged their 8-week treatment to be preferable compared with their previous treatments.

CONCLUSION

Results of this blinded interim analysis indicate that the fixed combination of calcipotriol/betamethasone dipropionate gel is highly efficacious and preferred by the majority of analysed patients.

摘要

背景

银屑病是一种常见的慢性炎症性皮肤病,大多数患者疾病有限,采用局部药物治疗。然而,局部治疗的特殊属性,如制剂/化妆品特性或不方便的治疗方案,可能导致患者对局部治疗的偏好度较低。因此,强烈需要一种高效、易于使用且同时受到医生和患者青睐的局部药物。

目的

本双盲中期分析旨在评估卡泊三醇/倍他米松二丙酸酯凝胶固定复方制剂在每日一次治疗 8 周后,对大多数患者的疗效(从医生和患者的角度)以及患者的偏好度,这些患者患有活跃的、轻度至中度银屑病,尽管之前进行过局部银屑病治疗,但在研究入组前的 8 周内治疗无效。

方法

在这项为期 64 周的 IV 期、国际、多中心、随机、对照、前瞻性、平行组研究中,纳入了既往局部治疗失败(即在研究入组前 8 周内治疗无效)的活跃、轻度至中度银屑病成年患者。患者在第 1 至 8 周内每天使用一次药物,然后按照 SmPC 进行 56 周的维持治疗。对所有患者进行双盲中期分析,包括人口统计学数据、医生总体评估、新型患者自我总体评估(PsGA)和患者偏好问卷(PPQ)。

结果

共分析了 1795 例患者。第 8 周时,36.5%的医生认为患者的银屑病为清除/几乎清除。同样,基于患者的自我评估,34.2%的患者在第 8 周时的 PsGA 评分为清除/几乎清除。PPQ 分析表明,绝大多数患者认为他们 8 周的治疗比之前的治疗更可取。

结论

这项双盲中期分析的结果表明,卡泊三醇/倍他米松二丙酸酯凝胶固定复方制剂具有高度疗效,且大多数分析患者都倾向于使用该药物。

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