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5%外用氟尿嘧啶乳膏治疗光化性角化病的长期疗效:一项随机临床试验。

Long-term Efficacy of Topical Fluorouracil Cream, 5%, for Treating Actinic Keratosis: A Randomized Clinical Trial.

机构信息

Center for Dermatoepidemiology, Veterans Affairs (VA) Medical Center, Providence, Rhode Island2Department of Dermatology, Brown University, Providence, Rhode Island.

Dermatology, Bay Pines VA Healthcare System, Bay Pines, Florida4Department of Internal Medicine (Dermatology), NOVA Southeastern University College of Osteopathic Medicine, Davie, Florida.

出版信息

JAMA Dermatol. 2015 Sep;151(9):952-60. doi: 10.1001/jamadermatol.2015.0502.

Abstract

IMPORTANCE

Topical fluorouracil was demonstrated to be effective in reducing the number of actinic keratoses (AKs) for up to 6 months, but no randomized trials studied its long-term efficacy.

OBJECTIVE

To evaluate the long-term efficacy of a single course of fluorouracil cream, 5%, for AK treatment.

DESIGN, SETTING, AND PARTICIPANTS: The Veterans Affairs Keratinocyte Carcinoma Chemoprevention (VAKCC) trial was a randomized, double-blinded, placebo-controlled trial with patients from dermatology clinics at 12 VA medical centers recruited from 2009 to 2011 and followed up until 2013. Our study population comprised 932 veterans with 2 or more keratinocyte carcinomas in the 5 years prior to enrollment. The mean follow-up duration was 2.6 years in both treatment and control groups.

INTERVENTIONS

Participants applied either topical fluorouracil cream, 5% (n = 468), or vehicle control cream (n = 464) to the face and ears twice daily for up to 4 weeks.

MAIN OUTCOMES AND MEASURES

This study reports on AK counts and treatments, which were secondary outcomes of the VAKCC trial. Actinic keratoses on the face and ears were counted by study dermatologists at enrollment and at study visits every 6 months. The number of spot treatments for AKs on the face and ears at semiannual study visits and in between study visits was recorded.

RESULTS

The number of AKs on the face and ears per participant was not different between the fluorouracil and control groups at randomization (11.1 vs 10.6, P > .10). After randomization, the fluorouracil group had fewer AKs compared with the control group at 6 months (3.0 vs 8.1, P < .001) and for the overall study duration (P < .001). The fluorouracil group also had higher complete AK clearance rates (38% vs 17% at 6 months) and fewer spot treatments at 6-month intervals, at study visits, and in between study visits during the trial (P < .01 for all). The fluorouracil group took longer to require the first spot AK treatment (6.2 months) compared with the control group (6.0 months) (hazard ratio, 0.69; 95% CI, 0.60-0.79). The number of hypertrophic AKs was not different between the 2 groups overall (P = .60), although there were fewer hypertrophic AKs in the fluorouracil group at 6 months (0.23 vs 0.41) (P = .05).

CONCLUSIONS AND RELEVANCE

Our results indicate that a single course of fluorouracil cream, 5%, effectively reduces AK counts and the need for spot treatments for longer than 2 years.

TRIAL REGISTRATION

clinicaltrials.gov Identifier:NCT00847912.

摘要

重要性

已有研究证实,局部使用氟尿嘧啶可有效减少多达 6 个月的光化性角化病(AK)数量,但尚无随机试验研究其长期疗效。

目的

评估氟尿嘧啶乳膏(浓度 5%)单次疗程治疗 AK 的长期疗效。

设计、地点和参与者:退伍军人事务部角质细胞癌化学预防(VAKCC)试验是一项随机、双盲、安慰剂对照试验,在 2009 年至 2011 年期间从 12 个退伍军人事务部医疗中心的皮肤科诊所招募患者,并随访至 2013 年。我们的研究人群包括 932 名在入组前 5 年内有 2 个或 2 个以上角质细胞癌的退伍军人。治疗组和对照组的平均随访时间均为 2.6 年。

干预措施

参与者将 5%氟尿嘧啶乳膏(n=468)或赋形剂乳膏(n=464)每日两次涂于面部和耳部,持续 4 周。

主要结局和测量指标

这是一项关于 AK 计数和治疗的研究,是 VAKCC 试验的次要结局。在入组时和每 6 个月的研究访视时,由研究皮肤科医生对面部和耳部的 AK 计数。记录面部和耳部 AK 的点治疗次数,以及研究访视之间和之间的次数。

结果

随机分组时,氟尿嘧啶组和对照组的面部和耳部 AK 数量无差异(11.1 对 10.6,P>.10)。随机分组后,氟尿嘧啶组与对照组相比,6 个月时 AK 数量较少(3.0 对 8.1,P<.001),整个研究期间也较少(P<.001)。氟尿嘧啶组完全清除 AK 的比例也更高(6 个月时为 38%,对 17%),在 6 个月的间隔、研究访视和研究访视之间的间隔期间,点治疗次数也较少(所有 P<.01)。氟尿嘧啶组首次需要进行 AK 点治疗的时间长于对照组(6.2 个月对 6.0 个月)(风险比,0.69;95%CI,0.60-0.79)。两组总体上肥厚性 AK 的数量无差异(P=.60),但氟尿嘧啶组 6 个月时肥厚性 AK 较少(0.23 对 0.41)(P=.05)。

结论和相关性

我们的结果表明,5%氟尿嘧啶乳膏单次疗程可有效减少 AK 数量,并在 2 年以上的时间内减少点治疗的需求。

试验注册

clinicaltrials.gov 标识符:NCT00847912。

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