Briatico Giulia, Brancaccio Gabriella, Scharf Camila, Di Brizzi Eugenia Veronica, Pellerone Sebastiano, Caccavale Stefano, Giorgio Caterina Mariarosaria, Procaccini Enrico Maria, Moscarella Elvira, Argenziano Giuseppe
Dermatology Unit, University of Campania, Naples, Italy.
Dermatol Pract Concept. 2023 Apr 1;13(2). doi: 10.5826/dpc.1302a151.
5-fluorouracil (5-FU) is one of the most effective topical treatments for actinic keratosis (AK). A new 4% formulation of 5-FU was recently approved in Europe.
This study aimed at evaluating 4% 5-FU cream safety and effectiveness in a real-world setting.
Adult AK patients were retrospectively selected from the University of Campania Dermatology Unit database. Selection criteria included a diagnosis of non-hyperkeratotic, non-hypertrophic AK (Olsen grade I and II) of the face, ears, and/or scalp, treatment with 4% 5-FU once daily for 4 weeks, and at least 3 follow-up visits (4 and 8 weeks after treatment initiation, and 6 months after treatment end). The primary objectives were to evaluate AK lesions improvement at 8 weeks and relapse rate at 6 months. Patient-reported erythema and burning sensation intensity were also assessed at 4 weeks.
Ninety-eight patients were included in this analysis (male/female 80/18, mean age 74.7 years). AK lesions improvement at 8 weeks resulted complete or significant in 74.5% and 20.4% of the patients, respectively. At 6 months, 65.3% of the patients did not show AK relapses. Burning sensation at 4 weeks was reported as light, moderate, or absent by 44.9%, 22.4%, and 31.6% of the patients, respectively. Erythema was reported as light, moderate, or absent by 37.8%, 51%, and 10% of the patients, respectively. Burning sensation and erythema disappeared gradually during follow-up. No other side effects were reported.
In this real-world study 4% 5-FU proved to be highly effective for AK lesions clearance with a favorable safety profile.
5-氟尿嘧啶(5-FU)是治疗光化性角化病(AK)最有效的局部治疗药物之一。一种新的4% 5-FU制剂最近在欧洲获得批准。
本研究旨在评估4% 5-FU乳膏在实际应用中的安全性和有效性。
从坎帕尼亚大学皮肤科数据库中回顾性选取成年AK患者。入选标准包括面部、耳部和/或头皮的非角化过度、非肥厚性AK(奥尔森I级和II级)诊断,每天一次使用4% 5-FU治疗4周,以及至少3次随访(治疗开始后4周和8周,治疗结束后6个月)。主要目的是评估8周时AK皮损的改善情况和6个月时的复发率。还在4周时评估了患者报告的红斑和烧灼感强度。
本分析纳入了98例患者(男性/女性为80/18,平均年龄74.7岁)。8周时,分别有74.5%和20.4%的患者AK皮损完全或显著改善。6个月时,65.3%的患者未出现AK复发。4周时,分别有44.9%、22.4%和31.6%的患者报告烧灼感为轻度、中度或无。分别有37.8%、51%和10%的患者报告红斑为轻度、中度或无。随访期间烧灼感和红斑逐渐消失。未报告其他副作用。
在这项实际研究中,4% 5-FU被证明对清除AK皮损非常有效,且安全性良好。