首页> 外文期刊>Journal of the American Academy of Dermatology >Randomized, double-blind, double-dummy, vehicle-controlled study of ingenol mebutate gel 0.025% and 0.05% for actinic keratosis.
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Randomized, double-blind, double-dummy, vehicle-controlled study of ingenol mebutate gel 0.025% and 0.05% for actinic keratosis.

机译:随机,双盲,双虚拟,媒介对照的丁香酚丁香醇凝胶0.025%和0.05%用于光化性角化病的媒介对照研究。

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BACKGROUND: There is a need for improved medical approaches to the treatment of actinic keratosis. Ingenol mebutate, a diterpene ester extracted and purified from the plant Euphorbia peplus, is being evaluated as a topical therapy for actinic keratosis. OBJECTIVE: Assess the efficacy and safety of ingenol mebutate (formerly PEP005) gel at 3 dosing regimens for the treatment of actinic keratosis. METHODS: Patients with non-facial actinic keratoses applied vehicle gel for 3 days, ingenol mebutate gel, 0.025% for 3 days, or ingenol mebutate gel, 0.05% for 2 or 3 days, with an 8-week follow-up period. RESULTS: All 3 active treatments were significantly more effective than vehicle at clearing actinic keratosis lesions, with a dose response observed. The partial clearance rate (primary efficacy end point) for patients treated with ingenol mebutate gel ranged from 56.0% to 75.4% compared with 21.7% for vehicle gel (P = .0002 to P < .0001 vs vehicle). The complete clearance rate was also significantly higher (P < or = .0006) for patients in the ingenol mebutate gel treatment groups (range: 40.0% to 54.4%) compared with vehicle (11.7%), as was the baseline clearance rate (range: 42.0% to 57.9% for ingenol mebutate gel compared with 13.3% for vehicle, P < .0001 to .0007 vs vehicle). The median percentage reduction in baseline actinic keratosis lesions for patients treated with ingenol mebutate gel ranged from 75% to 100% compared with 0% for vehicle gel (P < .0001 vs vehicle). Active treatment was well tolerated at all dosages. The mechanism of action of this agent is the localized induction of necrosis followed by a transient inflammatory response, and this was manifested in most patients as transient local skin responses consisting primarily of erythema, flaking/scaling, and crusting. There was no evidence of treatment-related scarring. LIMITATIONS: Local skin responses may have suggested active treatment to investigators. CONCLUSIONS: Short-course, field-directed therapy with ingenol mebutate gel for actinic keratoses on non-facial sites seems to be effective with a favorable safety profile and potential benefits over topical agents that require a more prolonged course of treatment.
机译:背景技术:需要改善的治疗光化性角化病的医学方法。甲磺酸丁二醇酯是从植物大戟属中提取和纯化的二萜酯,目前正在评估作为光化性角化病的局部治疗方法。目的:评估3种给药方案下甲磺酸丁二醇酯(以前的PEP005)凝胶治疗光化性角化病的疗效和安全性。方法:非面部光化性角化病患者应用赋形剂凝胶3天,丁二酸丁二醇酯凝胶,0.025%3天,或丁二酸丁二醇酯凝胶,0.05%2或3天,随访8周。结果:在清除光化性角化病病变方面,所有3种积极治疗均显着优于媒介物,并观察到剂量反应。丁二醇甲磺酸丁二醇酯凝胶治疗的患者的部分清除率(主要功效终点)为56.0%至75.4%,而赋形剂凝胶的部分清除率为21.7%(相对于赋形剂,P = .0002至P <.0001)。丁二醇甲磺酸丁二醇酯治疗组患者的完全清除率(P <或= .0006)也显着高于媒介物(11.7%)(范围:40.0%至54.4%),基线清除率(范围:丁香酚丁酸酯凝胶为42.0%至57.9%,而赋形剂为13.3%,相对于赋形剂,P <.0001至.0007)。丁二酸丁二醇酯凝胶治疗的患者基线光化性角化病病变的中位数降低幅度为75%至100%,而媒介物凝胶为0%(与媒介物相比P <.0001)。在所有剂量下,积极治疗的耐受性都很好。该药物的作用机制是局部诱导坏死,随后是短暂的炎症反应,这在大多数患者中表现为短暂的局部皮肤反应,主要由红斑,剥落/结皮和结cru组成。没有证据表明与治疗有关的瘢痕形成。局限性:局部皮肤反应可能已建议研究者积极治疗。结论:肌醇丁酸羟丁酯凝胶对非面部部位的光化性角化病进行短程,田间定向治疗似乎是有效的,其安全性和潜在益处优于需要更长疗程的局部用药。

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