Comparison of topical 5-fluorouracil formulations in actinic keratosis treatment

被引:24
|
作者
Kaur, Ravneet R. [1 ]
Alikhan, Ali [2 ]
Maibach, Howard I. [3 ]
机构
[1] Univ Calif Los Angeles, Sch Med, Los Angeles, CA USA
[2] Univ Calif Davis, Sch Med, Davis, CA 95616 USA
[3] Univ Calif San Francisco, San Francisco, CA 94143 USA
关键词
actinic keratosis; Carac (R); Efudex (R); topical; 5-fluorouracil; 5-FU; 35-PERCENT TRICHLOROACETIC-ACID; 0.5-PERCENT FLUOROURACIL CREAM; 5-PERCENT FLUOROURACIL; JESSNERS SOLUTION; EFFICACY; CRYOSURGERY; IMIQUIMOD; SAFETY; 1-WEEK;
D O I
10.3109/09546630903341937
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Background: Actinic keratoses (AKs) are common and may progress to squamous cell carcinoma (SCC). While cryotherapy is the most commonly used treatment for AKs, it is only suitable for treating a few lesions at a time. Topical medications such as 5-fluorouracil (5-FU) allow for more generalized treatment of AKs in the setting of multiple lesions. Objective: To evaluate and discuss clinical trials examining the efficacy of 5-FU cream formulations (0.5% and 5%), as 5% 5-FU has four times greater systemic absorption. Methods: We conducted Pubmed and Embase searches (1965 to 13 April 2009) to find studies evaluating the efficacy of 5-FU cream monotherapy (0.5% and 5%) in treating multiple AKs of the face and scalp. We only included studies employing standard treatment regimens (as per the US FDA), with an endpoint of complete clearance. Results: Nine studies met our criteria. At 4 weeks post-treatment, complete clearance rates of 0.5% and 5% 5-FU ranged from 16.7% to 57.8% and 43% to 100%, respectively. As the various studies employed different measurements of tolerability, we were unable to pool this data. In the only split-face study comparing both formulations, both treatments produced equivalent rates (43%) of complete clearance, but 5% 5-FU had higher rates of adverse events. Conclusions: Despite evidence suggesting the superior efficacy of 5% 5-FU over 0.5% 5-FU, high-powered clinical trials comparing both treatments are lacking. Furthermore, tolerability rates between formulations warrant further examination given the possible enhanced systemic absorption of 5% 5-FU over 0.5% 5-FU. Such studies will enable dermatologists to appropriately balance the risks and benefits of each respective treatment to provide optimal solutions to patients with multiple AKs.
引用
收藏
页码:267 / 271
页数:5
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