Glaser D A, Hossain P, Perkins W, Griffiths T, Ahluwalia G, Weng E, Beddingfield F C
Department of Dermatology, Saint Louis University, St Louis, MO, U.S.A.
NIHR Wellcome Trust Clinical Research Facility, Southampton General Hospital, University of Southampton, Southampton, U.K.
Br J Dermatol. 2015;172(5):1384-94. doi: 10.1111/bjd.13443. Epub 2015 Mar 7.
Bimatoprost ophthalmic solution 0·03% is approved in several countries for the treatment of eyelash hypotrichosis. Previous trials were limited to 4 months of treatment and primarily idiopathic hypotrichosis.
To evaluate the long-term safety and efficacy of bimatoprost in patients with idiopathic or chemotherapy-induced hypotrichosis.
This multicentre, double-masked, randomized, parallel-group study included two 6-month treatment periods [treatment period 1 (TP1) and treatment period 2 (TP2)]. Patients with idiopathic hypotrichosis were randomized to three treatment groups: (i) bimatoprost (TP1 and TP2); (ii) bimatoprost (TP1) and vehicle (TP2); and (iii) vehicle (TP1) and bimatoprost (TP2). Patients with chemotherapy-induced hypotrichosis were randomized to two treatment groups: (i) bimatoprost or vehicle (TP1) and (ii) bimatoprost (TP2). Primary end point was a composite of at least a one-grade improvement in investigator-assessed Global Eyelash Assessment and at least a three-point improvement in patient-reported Eyelash Satisfaction Questionnaire Domain 2 at month 4. Secondary measures included digitally assessed eyelash characteristics.
The primary efficacy end point was met in both populations (idiopathic responder rate was 40·2% for bimatoprost vs. 6·8% for vehicle; postchemotherapy responder rate was 37·5% for bimatoprost vs. 18·2% for vehicle). Efficacy by month 6 was maintained (idiopathic) or enhanced (postchemotherapy) at 12 months. Treatment effects were maintained for approximately 2 months but markedly diminished 4-6 months following treatment cessation in patients with idiopathic hypotrichosis. No drug-related serious adverse events were reported.
Daily treatment with bimatoprost ophthalmic solution 0·03% for 1 year was effective and well tolerated in patients with idiopathic and chemotherapy-induced hypotrichosis.
0.03%的比马前列素滴眼液已在多个国家获批用于治疗睫毛稀少症。以往试验的治疗时间限制在4个月,且主要针对特发性睫毛稀少症。
评估比马前列素治疗特发性或化疗所致睫毛稀少症患者的长期安全性和疗效。
这项多中心、双盲、随机、平行组研究包括两个6个月的治疗期[治疗期1(TP1)和治疗期2(TP2)]。特发性睫毛稀少症患者被随机分为三个治疗组:(i)比马前列素组(TP1和TP2);(ii)比马前列素组(TP1)和赋形剂组(TP2);(iii)赋形剂组(TP1)和比马前列素组(TP2)。化疗所致睫毛稀少症患者被随机分为两个治疗组:(i)比马前列素或赋形剂组(TP1)和(ii)比马前列素组(TP2)。主要终点是在第4个月时,研究者评估的全球睫毛评估至少提高一级,且患者报告的睫毛满意度问卷领域2至少提高3分。次要指标包括数字化评估的睫毛特征。
两个群体均达到主要疗效终点(特发性患者中,比马前列素组的缓解率为40.2%,赋形剂组为6.8%;化疗后患者中,比马前列素组的缓解率为37.5%,赋形剂组为18.2%)。6个月时的疗效在12个月时得以维持(特发性患者)或增强(化疗后患者)。特发性睫毛稀少症患者治疗效果维持约2个月,但在停药后4 - 6个月明显减弱。未报告与药物相关的严重不良事件。
0.03%的比马前列素滴眼液每日治疗1年,对特发性和化疗所致睫毛稀少症患者有效且耐受性良好。