Bieber T, Vick K, Fölster-Holst R, Belloni-Fortina A, Städtler G, Worm M, Arcangeli F
Department of Dermatology, University of Bonn, Bonn, Germany.
Allergy. 2007 Feb;62(2):184-9. doi: 10.1111/j.1398-9995.2006.01269.x.
Topical glucocorticosteroids are the gold standard in treatment of atopic dermatitis (AD). Recently, topical calcineurin inhibitors have been developed for treatment of this condition. This study compared efficacy and safety of 0.1% methylprednisolone aceponate (MPA) ointment with 0.03% tacrolimus ointment for 3 weeks, in children and adolescents with severe to very severe flare of AD.
The primary end point was treatment success, defined as a score of 'clear' or 'almost clear' in the static Investigator's Global Assessment (IGA) score. Secondary end points were the percentage change in the Eczema Area and Severity Index (EASI) and patients' assessment of itch and sleep, Children's Dermatology Life Quality Index, patient's assessment of global response, affected Body Surface Area and medication costs.
265 patients were randomized to either MPA (n = 129) or tacrolimus (n = 136) treatment, 257 patients completed the study. Methylprednisolone aceponate 0.1% ointment once daily provided rapid and relevant clinical benefit. Tacrolimus 0.03% ointment twice daily was equally effective with regard to success rate. Methylprednisolone aceponate was superior to tacrolimus for EASI, itch and sleep. Both treatments were well tolerated. Drug-related adverse events were only observed in the tacrolimus group. Medication costs were significantly lower for MPA.
While both treatment groups showed similar efficacy results regarding treatment success (IGA), significant advantages were observed for EASI, itch and sleep with MPA 0.1%. These advantages and the significantly lower treatment costs highlight the benefits of MPA treatment, underlining its first-line role in treatment of children and adolescents with severe AD.
外用糖皮质激素是治疗特应性皮炎(AD)的金标准。最近,外用钙调神经磷酸酶抑制剂已被开发用于治疗这种疾病。本研究比较了0.1%糠酸莫米松(MPA)软膏和0.03%他克莫司软膏对重度至极重度AD发作的儿童和青少年进行3周治疗的疗效和安全性。
主要终点是治疗成功,定义为静态研究者整体评估(IGA)评分为“清除”或“几乎清除”。次要终点是湿疹面积和严重程度指数(EASI)的变化百分比、患者对瘙痒和睡眠的评估、儿童皮肤病生活质量指数、患者对整体反应的评估、受累体表面积和药物成本。
265例患者被随机分为MPA组(n = 129)或他克莫司组(n = 136)进行治疗,257例患者完成了研究。每日一次外用0.1%糠酸莫米松软膏可提供快速且显著的临床益处。每日两次外用0.03%他克莫司软膏在成功率方面同样有效。在EASI、瘙痒和睡眠方面,糠酸莫米松优于他克莫司。两种治疗耐受性均良好。仅在他克莫司组观察到与药物相关的不良事件。MPA的药物成本显著更低。
虽然两个治疗组在治疗成功(IGA)方面显示出相似的疗效结果,但0.1%MPA在EASI、瘙痒和睡眠方面具有显著优势。这些优势以及显著更低的治疗成本凸显了MPA治疗的益处,强调了其在治疗重度AD儿童和青少年中的一线作用。