Gupta A K, Weiss J S, Jorizzo J L
Division of Dermatology, Department of Medicine, Sunnybrook and Womens' College Health Sciences Center (Sunnybrook Site), and the University of Toronto, Toronto, Ontario, Canada.
Skin Therapy Lett. 2001 Jun;6(9):1-4.
Carac (5-fluorouracil 0.5% cream, Aventis Pharma) was approved by the US FDA in October 2000, for the treatment of multiple actinic or solar keratoses involving the face and anterior scalp. The cream should be applied in a thin film once daily to the skin where actinic keratoses (AKs) are present. When it is applied for 1, 2, or 4 weeks, it is significantly more effective than a vehicle in the management of patients with five or more AKs at pretherapy. Pooled data from the two pivotal trials (n=384) indicate that following 4 weeks of therapy the number of subjects with total AK clearance in the Carac and vehicle groups was 52.9% and 1.6% respectively (p<0.001). Furthermore, the corresponding reduction of AK lesion counts in the Carac and vehicle groups was 82.5% and 19.3%, respectively (p<0.001). Treatment should be continued up to 4 weeks as tolerated by the patient. The most common adverse-effect is facial irritation.
卡拉克(5%氟尿嘧啶乳膏,安万特制药公司生产)于2000年10月获美国食品药品监督管理局批准,用于治疗累及面部和头皮前部的多发性光化性或日光性角化病。该乳膏应每天在出现光化性角化病(AK)的皮肤上涂抹薄薄一层。在治疗前患有5个或更多AK的患者中,使用1周、2周或4周时,其治疗效果显著优于赋形剂。两项关键试验(n = 384)的汇总数据表明,治疗4周后,卡拉克组和赋形剂组中AK完全清除的受试者比例分别为52.9%和1.6%(p<0.001)。此外,卡拉克组和赋形剂组中AK皮损数量的相应减少率分别为82.5%和19.3%(p<0.001)。应根据患者耐受情况持续治疗长达4周。最常见的不良反应是面部刺激。