Department of Dermatology, Seoul National University College of Medicine, 28-Yongon-dong, Chongno-gu, Seoul 110-744, Korea.
Br J Dermatol. 2010 Jun;162(6):1359-64. doi: 10.1111/j.1365-2133.2010.09758.x. Epub 2010 Mar 10.
Facial psoriasis gives rise to considerable concern because of associated cosmetic problems and psychosocial distress. It requires a treatment approach other than topical corticosteroids, which bear a risk of cutaneous adverse reactions. Recently, topical tacalcitol has been shown to be effective in psoriasis.
The aim of this open-label single-centre study is to investigate the efficacy and safety of high-concentration (20 μg g⁻¹) ) tacalcitol ointment (Bonalfa-high(®) , Teijin Pharma, Tokyo, Japan) in patients with facial psoriasis and to evaluate clinical response according to the distribution of facial psoriatic lesions.
Thirty-seven patients were enrolled to this clinical trial. Tacalcitol 20 μg g⁻¹ ointment was applied once daily to psoriatic lesions of the face over an 8-week period. Patients were also categorized into three subtypes according to facial lesion distribution. Efficacy was evaluated by the facial Psoriasis Area and Severity Index (facial PASI) and the Physician's Global Assessment (PGA) score at weeks 2, 4 and 8. The Subjective Global Assessment (SGA) was also determined at the end of the study.
Thirty-three patients completed the clinical trial. Mean facial PASI of 33 patients at baseline was 9·58 and after 8 weeks of treatment the mean facial PASI decreased significantly to 3·88. By using PGA, patients showed the following responses to treatment: clearance (n = 1); excellent (6); good (16); fair (4); slight (5); no change (1). The response rate among the three facial psoriasis types showed no difference. Using the SGA, 27 (82%) of the patients presented excellent (15%) or good (67%) effect with tacalcitol 20 μg g⁻¹ ointment. No serious adverse reactions were observed.
This is the first clinical study reporting a relevant therapeutic effect and favourable safety profile of tacalcitol 20 μg g⁻¹ ointment in facial psoriasis. These results suggest that tacalcitol 20 μg g⁻¹ ointment can be used as the first-line treatment in patients with facial psoriasis.
面部银屑病会引起严重的关注,因为它与美容问题和心理社会困扰有关。它需要一种治疗方法,而不是局部皮质类固醇,因为后者会有皮肤不良反应的风险。最近,局部他卡西醇已被证明对银屑病有效。
本开放性单中心研究旨在探讨高浓度(20μg g⁻¹)他卡西醇软膏(Bonalfa-high®,日本帝人制药)治疗面部银屑病患者的疗效和安全性,并根据面部银屑病病变的分布评估临床疗效。
本临床试验共纳入 37 例患者。将他卡西醇 20μg g⁻¹软膏应用于面部银屑病皮损,每天一次,持续 8 周。根据面部病变分布,患者还分为三个亚型。在第 2、4 和 8 周时,通过面部银屑病面积和严重程度指数(facial PASI)和医生整体评估(PGA)评分评估疗效。在研究结束时还进行了主观整体评估(SGA)。
33 例患者完成了临床试验。33 例患者的基线面部 PASI 平均值为 9.58,治疗 8 周后,平均面部 PASI 显著下降至 3.88。根据 PGA,患者的治疗反应如下:痊愈(n = 1);极好(6);好(16);中(4);轻(5);无变化(1)。三种面部银屑病类型的反应率无差异。使用 SGA,27(82%)例患者对他卡西醇 20μg g⁻¹软膏的治疗效果为极好(15%)或良好(67%)。未观察到严重不良反应。
这是第一项关于他卡西醇 20μg g⁻¹软膏对面部银屑病具有相关治疗效果和良好安全性的临床研究。这些结果表明,他卡西醇 20μg g⁻¹软膏可作为面部银屑病患者的一线治疗药物。