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首页> 外文期刊>Journal of the European Academy of Dermatology and Venereology: JEADV >Open label randomized study comparing 3 months vs. 6 months treatment of actinic keratoses with 3% diclofenac in 2.5% hyaluronic acid gel: a trial of the German Dermatologic Cooperative Oncology Group.
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Open label randomized study comparing 3 months vs. 6 months treatment of actinic keratoses with 3% diclofenac in 2.5% hyaluronic acid gel: a trial of the German Dermatologic Cooperative Oncology Group.

机译:开放标签的随机研究比较了在2.5%透明质酸凝胶中使用3%双氯芬酸治疗3个月和6个月的光化性角化病:德国皮肤病学合作肿瘤小组的一项试验。

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BACKGROUND: Actinic keratoses (AK) are carcinomata in situ with the potential to develop into invasive carcinoma. Several studies have demonstrated that 3% diclofenac in 2.5% hyaluronic acid gel (HA) is effective and well tolerated in the treatment of AK. To date there are no large randomized multicentre trials with treatment durations longer than 90 days and histopathological control of treatment outcome. OBJECTIVE: The aim of this study was to investigate whether a prolonged treatment with diclofenac in HA of 6 vs. 3 months adds to the efficacy in treatment for AK and if this will influence tolerability and quality of life (QoL). METHODS: This was a multicentre, randomized open-label study in which 418 patients with mild to moderate AKs were randomized into two treatment groups. Group A received diclofenac in HA for 3 months and group B for 6 months. Treatment efficacy was assessed by size measurement and a final biopsy of a defined marker AK. Quality of life was measured using the Dermatology Life Quality Index questionnaire. RESULTS: Clinical complete clearance was observed in 40% in group A and in 45% in group B (P = 0.38). Histopathological clearance was confirmed in 30% in group A and in 40% in group B (P = 0.16). Treatment was well tolerated and QoL was significantly improved after treatment in both treatment groups. CONCLUSION: Treatment with diclofenac in HA is effective and well tolerated during a treatment period of 3 months as well as 6 months. Prolongation of the treatment duration did not significantly affect treatment outcome.
机译:背景:光化性角化病(AK)是原位癌,可能发展为浸润性癌。几项研究表明,在2.5%的透明质酸凝胶(HA)中使用3%的双氯芬酸是有效的,并且具有很好的耐受性。迄今为止,尚无大型的多中心随机试验,其治疗时间超过90天且对治疗结局进行了组织病理学控制。目的:本研究的目的是调查双氯芬酸在HA中进行6个月与3个月的长期治疗是否能增加AK的治疗效果,以及这是否会影响耐受性和生活质量(QoL)。方法:这是一项多中心,随机开放标签研究,其中将418例轻至中度AK患者随机分为两个治疗组。 A组在HA中接受双氯芬酸3个月,B组接受6个月。通过尺寸测量和确定的标记物AK的最终活检评估治疗效果。使用皮肤病生活质量指数调查表测量生活质量。结果:A组有40%的临床完全清除率,B组有45%的临床完全清除率(P = 0.38)。 A组中30%的人确认了组织病理学清除率,B组中40%的人确认了组织病理学清除率(P = 0.16)。在两个治疗组中,治疗耐受性良好,生活质量明显改善。结论:在3个月和6个月的治疗期内,双氯芬酸在HA中的治疗均有效且耐受性良好。治疗时间的延长不会显着影响治疗效果。

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