Bettencourt Miriam S
Advanced Dermatology and Cosmetic Surgery, Henderson, Nevada; Assistant Clinical Professor of Dermatology, University of Nevada, Las Vegas, Nevada.
J Clin Aesthet Dermatol. 2016 Mar;9(3):20-4. Epub 2016 Mar 1.
To describe the safety, tolerability, and efficacy of treatment of actinic keratosis on the scalp with two consecutive, once-daily applications of ingenol mebutate gel, 0.05%.
Retrospective chart review.
Community dermatology practice.
Male patients (N=78) with a long history of recurrent and relapsed scalp actinic keratosis.
This chart review extracted non-identifying information on patients' medical history, pertinent history of actinic keratosis and skin cancer, and prior actinic keratosis treatments. Also collected was information on patients' treatment of scalp actinic keratosis with ingenol mebutate gel, 0.05%, including the occurrence of local skin reactions and their treatment, adverse events, and efficacy results at short-term and additional follow-up.
In these patients, a significant proportion of the scalp had numerous actinic keratoses that were often recurrent and/or hyperkeratotic. Most patients (83%) received cryosurgery to visible scalp actinic keratoses two weeks before ingenol mebutate treatment. Local skin reactions developed on the first day of topical treatment, were predominantly mild or moderate in intensity, and generally were resolved by 10 to 14 days. Local skin reactions were treated with a topical moisturizing product in 44 percent of the patients. Nearly half (45%) of the patients experienced application-site reactions, described as a combination of burning, itching, pain, and/or tenderness; the reactions were mild or moderate in intensity and lasted only a few days.
Ingenol mebutate gel, 0.05%, had a good safety and tolerability profile when used to treat scalp actinic keratosis in patients who had a prolonged history of actinic keratosis.
描述连续两日每日一次外用0.05% ingenol mebutate凝胶治疗头皮光化性角化病的安全性、耐受性和疗效。
回顾性病历审查。
社区皮肤科诊所。
有复发性和复发性头皮光化性角化病病史的男性患者(N = 78)。
本次病历审查提取了患者病史、光化性角化病和皮肤癌相关病史以及既往光化性角化病治疗的非识别性信息。还收集了患者使用0.05% ingenol mebutate凝胶治疗头皮光化性角化病的信息,包括局部皮肤反应的发生情况及其治疗、不良事件以及短期和额外随访的疗效结果。
在这些患者中,很大一部分头皮有大量光化性角化病,且常复发和/或角化过度。大多数患者(83%)在使用ingenol mebutate治疗前两周接受了冷冻手术治疗可见的头皮光化性角化病。局部皮肤反应在局部治疗的第一天出现,强度主要为轻度或中度,一般在10至14天内消退。44%的患者使用局部保湿产品治疗局部皮肤反应。近一半(45%)的患者出现用药部位反应,表现为灼痛、瘙痒、疼痛和/或压痛的组合;反应强度为轻度或中度,仅持续数天。
0.05% ingenol mebutate凝胶用于治疗有长期光化性角化病病史患者的头皮光化性角化病时,具有良好的安全性和耐受性。