Center for Dermatoepidemiology, Veterans Affairs (VA) Medical Center, Providence, Rhode Island.
Department of Dermatology, The Warren Alpert Medical School of Brown University, Providence, Rhode Island.
JAMA Dermatol. 2018 Feb 1;154(2):167-174. doi: 10.1001/jamadermatol.2017.3631.
Keratinocyte carcinoma (ie, cutaneous basal and squamous cell carcinoma) is the most common cancer in the United States.
To determine whether topical fluorouracil could prevent surgically treated keratinocyte carcinoma.
DESIGN, SETTING, AND PARTICIPANTS: The Veterans Affairs Keratinocyte Carcinoma Chemoprevention Trial was a randomized, double-blind, placebo-controlled trial of topical fluorouracil for chemoprevention of keratinocyte carcinoma. Participants were recruited from May 2009 to September 2011 from 12 Veterans Affairs medical centers and followed until June 30, 2013. Participants were veterans (n = 932) with a history of at least 2 keratinocyte carcinomas in the past 5 years; almost all were white males and the median age was 70 years.
Application of fluorouracil, 5%, (n = 468) or vehicle control cream (n = 464) to the face and ears twice daily for 2 to 4 weeks upon randomization.
Surgically treated keratinocyte, basal cell, and squamous cell carcinoma risk on the face and ears in the first year after enrollment; and time to first surgically treated keratinocyte, basal cell, and squamous cell carcinoma. The a priori hypothesis was that fluorouracil would be effective in preventing these cancers.
Of 932 participants (916 men [98%]; 926 white [99%]; median age, 70 years), 299 developed a basal cell carcinoma end point (95 in year 1) and 108 developed a squamous cell carcinoma end point (25 in year 1) over 4 years (median follow-up, 2.8 years). Over the entire study, there was no difference between treatment groups in time to first keratinocyte, basal cell, or squamous cell carcinoma. During the first year, however, 5 participants (1%) in the fluorouracil group developed a squamous cell carcinoma vs 20 (4%) in the control group, a 75% (95% CI, 35%-91%) risk reduction (P = .002). The 11% reduction in basal cell carcinoma risk during year 1 (45 [10%] in the fluorouracil group vs 50 [11%] in the control group) was not statistically significant (95% CI, 39% reduction to 31% increase), nor was there a significant effect on keratinocyte carcinoma risk. However, a reduction in keratinocyte carcinomas treated with Mohs surgery was observed.
A conventional course of fluorouracil to the face and ears substantially reduces surgery for squamous cell carcinoma for 1 year without significantly affecting the corresponding risk for basal cell carcinoma.
clinicaltrials.gov Identifier: NCT00847912.
角朊细胞癌(即皮肤基底细胞和鳞状细胞癌)是美国最常见的癌症。
确定局部氟尿嘧啶是否可预防经手术治疗的角朊细胞癌。
设计、地点和参与者:退伍军人事务部角朊细胞癌化学预防试验是一项随机、双盲、安慰剂对照的研究,旨在研究局部氟尿嘧啶对角朊细胞癌的化学预防作用。参与者于 2009 年 5 月至 2011 年 9 月从 12 个退伍军人事务医疗中心招募,并随访至 2013 年 6 月 30 日。参与者为(n=932)有过去 5 年内至少 2 次经手术治疗的角朊细胞癌病史的退伍军人;几乎均为白人男性,中位年龄为 70 岁。
随机分组后,每天两次将氟尿嘧啶(浓度为 5%)(n=468)或载体对照乳膏(n=464)涂于面部和耳部,持续 2 至 4 周。
入组后第 1 年面部和耳部经手术治疗的角朊细胞、基底细胞和鳞状细胞癌风险;以及首次经手术治疗的角朊细胞、基底细胞和鳞状细胞癌的时间。预先假设氟尿嘧啶可有效预防这些癌症。
在 932 名参与者(916 名男性[98%];926 名白人[99%];中位年龄为 70 岁)中,299 名参与者发生了基底细胞癌终点事件(95 名在第 1 年),108 名参与者发生了鳞状细胞癌终点事件(25 名在第 1 年),随访时间为 4 年(中位随访时间为 2.8 年)。在整个研究过程中,治疗组间角朊细胞、基底细胞或鳞状细胞癌的发生时间无差异。然而,在第 1 年期间,氟尿嘧啶组有 5 名(1%)参与者发生了鳞状细胞癌,而对照组有 20 名(4%),风险降低了 75%(95%CI,35%-91%)(P=0.002)。第 1 年基底细胞癌风险降低 11%(氟尿嘧啶组 45 例[10%],对照组 50 例[11%])无统计学意义(95%CI,39%降低至 31%增加),角朊细胞癌风险也无显著影响。然而,Mohs 手术治疗的角朊细胞癌数量有所减少。
常规使用氟尿嘧啶对面部和耳部进行治疗可在 1 年内显著减少鳞状细胞癌的手术治疗,而不会显著影响相应的基底细胞癌风险。
clinicaltrials.gov 标识符:NCT00847912。