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一项多中心、随机、双盲、平行分组、赋形剂对照的 IIb 期研究,旨在评估 1%和 3%外用盐酸米诺环素凝胶治疗丘疹脓疱性酒渣鼻患者的安全性和有效性。

A multicentre, randomized, double-masked, parallel group, vehicle-controlled phase IIb study to evaluate the safety and efficacy of 1% and 3% topical minocycline gel in patients with papulopustular rosacea.

机构信息

Department of Dermatology, Sidney Kimmel Medical College of Thomas Jefferson University, Philadelphia, PA, USA.

Dermatology Consulting Services, High Point, NC, USA.

出版信息

Br J Dermatol. 2020 Sep;183(3):471-479. doi: 10.1111/bjd.18857. Epub 2020 Apr 14.

Abstract

BACKGROUND

Papulopustular rosacea is characterized by chronic facial erythema and inflammatory facial lesions. Minocycline has anti-inflammatory properties which may be effective in the treatment of rosacea inflammatory lesions.

OBJECTIVES

To assess the safety and efficacy of once-daily topical minocycline gel 1% and 3% in patients with papulopustular rosacea.

METHODS

This was a prospective, 12-week, double-blinded study conducted at 26 sites in the United States; 270 patients with papulopustular rosacea and 12-40 inflammatory lesions were randomized to minocycline 1%, minocycline 3% or vehicle. The primary endpoint was the mean change in inflammatory lesions at week 12. Key secondary endpoints included success on an Investigator's Global Assessment (IGA).

RESULTS

Baseline mean lesion counts were 24·6, 25·1 and 24·3 in the minocycline 1%, minocycline 3% and vehicle groups, respectively; at week 12, the counts had decreased by 12·6, 13·1 and 7·9, respectively. Minocycline significantly decreased lesions, compared with the vehicle [P = 0·01, 95% confidence interval (CI) 7·9 to 0·9, for minocycline 1%; P = 0·007, 95% CI 8·3 to 1·3, for minocycline 3%]. The proportion of patients achieving IGA success was 39% in the minocycline 1% arm [P = 0·34, odds ratio (OR) 1·396 and OR 95% CI 0·71 to 2·75 vs. vehicle], 46% in the minocycline 3% arm (P = 0·04, OR 2·03 and OR 95% CI 1·04 to 3·95 vs. vehicle) and 31% in the vehicle arm.

CONCLUSIONS

Minocycline topical gel appears to be safe and tolerable at concentrations of 1% and 3%, and both concentrations significantly decreased inflammatory lesion counts, with a significantly larger proportion of patients achieving IGA success at week 12 in the minocycline 3% arm. These findings support further evaluation of minocycline gel for treating inflammatory lesions associated with papulopustular rosacea. Linked Comment: Hampton. Br J Dermatol 2020; 183:412-413.

摘要

背景

脓疱性酒渣鼻的特征为慢性面部红斑和炎症性面部皮损。米诺环素具有抗炎特性,可能对酒渣鼻炎症性皮损的治疗有效。

目的

评估 1%和 3%浓度的米诺环素凝胶每日 1 次外用治疗脓疱性酒渣鼻的安全性和疗效。

方法

这是一项在美国 26 个地点进行的前瞻性、12 周、双盲研究;270 例脓疱性酒渣鼻患者和 12-40 个炎症性皮损随机分为米诺环素 1%组、米诺环素 3%组或赋形剂组。主要终点为第 12 周时炎症性皮损的平均变化。关键次要终点包括研究者总体评估(IGA)的疗效。

结果

米诺环素 1%、米诺环素 3%和赋形剂组的基线平均皮损数分别为 24.6、25.1 和 24.3;第 12 周时,皮损数分别减少了 12.6、13.1 和 7.9。与赋形剂组相比,米诺环素组皮损显著减少[P=0.01,95%置信区间(CI)为 7.9 至 0.9,米诺环素 1%组;P=0.007,95%CI 为 8.3 至 1.3,米诺环素 3%组]。米诺环素 1%组的 IGA 疗效成功比例为 39%[P=0.34,比值比(OR)为 1.396,95%CI 为 0.71 至 2.75 与赋形剂组相比],米诺环素 3%组为 46%(P=0.04,OR 为 2.03,95%CI 为 1.04 至 3.95 与赋形剂组相比),赋形剂组为 31%。

结论

米诺环素外用凝胶的浓度为 1%和 3%时似乎安全且耐受良好,两者均能显著减少炎症性皮损数量,米诺环素 3%组在第 12 周时 IGA 疗效成功的患者比例显著更大。这些发现支持进一步评估米诺环素凝胶治疗脓疱性酒渣鼻相关炎症性皮损。

相关评论

Hampton. Br J Dermatol 2020; 183:412-413.

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4478/7496252/e2139926695c/BJD-183-471-g001.jpg

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