Stein Gold Linda, Kircik Leon, Fowler Joseph, Jackson J Mark, Tan Jerry, Draelos Zoe, Fleischer Alan, Appell Melanie, Steinhoff Martin, Lynde Charles, Sugarman Jeffrey, Liu Hong, Jacovella Jean
J Drugs Dermatol. 2014 Nov;13(11):1380-6.
Papulopustular rosacea (PPR) is characterized by facial erythema and inflammatory lesions believed to be primarily caused by dysregulation of the innate immune system. More recent evidence also suggests that Demodex folliculorum mites may contribute to the etiology of PPR. Ivermectin (IVM) 1% cream is a novel topical treatment developed to treat PPR. Two phase 3 trials have demonstrated that IVM 1% cream was significantly better than vehicle at investigator global assessment (IGA) success rate and lesion reductions and that it was safe and well tolerated. Two 40-week extension studies of those trials were conducted to assess the long-term safety of IVM 1% cream vs azelaic acid (AzA) 15% gel. Subjects originally treated with IVM 1% continued on IVM 1% and those originally treated with vehicle switched to AzA 15% gel. IVM 1% cream was safe throughout the study with a lower incidence of related adverse events (AEs) compared to AzA 15% gel. No subjects in the IVM 1% cream group discontinued either study due to a related AE. IVM 1% also continued to be efficacious during the 40-week extension studies as the percentage of subjects with IGA scores of clear or almost clear was higher at the end of the study compared to baseline. The results of these 40-week extension studies support the use of IVM 1% cream as a long-term therapy for PPR as IVM 1% cream was shown to be safe and effective for up to 52 weeks of total treatment.
丘疹脓疱型玫瑰痤疮(PPR)的特征为面部红斑和炎症性皮损,据信主要由先天性免疫系统失调引起。最近的证据还表明,毛囊蠕形螨可能与PPR的病因有关。1%伊维菌素(IVM)乳膏是一种用于治疗PPR的新型局部治疗药物。两项3期试验表明,在研究者整体评估(IGA)成功率和皮损减少方面,1%IVM乳膏显著优于赋形剂,且其安全性良好、耐受性佳。对这些试验进行了两项为期40周的延长期研究,以评估1%IVM乳膏与15%壬二酸(AzA)凝胶的长期安全性。最初接受1%IVM治疗的受试者继续使用1%IVM,而最初接受赋形剂治疗的受试者改用15%AzA凝胶。在整个研究过程中,1%IVM乳膏安全,与15%AzA凝胶相比,相关不良事件(AE)的发生率更低。1%IVM乳膏组中没有受试者因相关AE而中断任何一项研究。在为期4周的延长期研究中,1%IVM继续有效,因为与基线相比,在研究结束时IGA评分为清除或几乎清除的受试者百分比更高。这些为期40周的延长期研究结果支持将1%IVM乳膏用作PPR的长期治疗方法,因为1%IVM乳膏在长达52周的总治疗期内均显示安全有效。