Oral Retinol, Alone or Combined with Medical Photoprotection, in Patients with Actinic Keratosis: A Randomized, Open-Label, Prospective, Multicentric Study.

IF 4.6 3区 医学 Q1 DERMATOLOGY
Marco Ardigò, Martina Burlando, Elena Campione, Gianluca Nazzaro, Giulio Foggi, Francesca Colombo, Stefano Alfano, Massimo Milani, Angelo V Marzano
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引用次数: 0

Abstract

Introduction: Actinic keratosis (AK) is a chronic ultraviolet-induced condition with potential progression to squamous cell carcinoma. This study assessed the efficacy and tolerability of oral retinol, alone or combined with broad-spectrum medical photoprotection containing piroxicam, in patients with mild-to-moderate AK.

Methods: In this multicenter, prospective, randomized, open-label study, 117 patients with up to six AK lesions were assigned to oral retinol 50,000 international units (IU)/day (group A), oral retinol plus medical photoprotection (group B), or standard photoprotection recommendations (group C). Treatment lasted 6 months, followed by 3 months of follow-up. Assessments were performed at baseline and at months 3, 6, and 9. The primary endpoint was change in Actinic Keratosis Area and Severity Index (AKASI). Secondary outcomes included global clinical efficacy, lesion clearance, tolerability, and exploratory line-field confocal optical coherence tomography findings.

Results: All 117 patients were included in the intention-to-treat analysis, and 99 in the per-protocol analysis. AKASI scores decreased significantly in group A at month 6 by - 19.3% (mean difference (MD) 0.61, 95% confidence interval (CI) 0.11-1.11; p < 0.05) and at month 9 by - 22.5% (MD 0.71, 95% CI 0.18-1.25; p < 0.01). In group B, significant reductions were observed at all time points (T3: - 24.1%; MD 0.90, 95% CI 0.42-1.39; p < 0.0001; T6: - 34.9%; MD 1.31, 95% CI 0.86-1.76; p < 0.0001; T9: - 38.8%; MD 1.45, 95% CI 0.95-1.95; p < 0.0001). No significant changes occurred in group C. Reductions were earlier and greater with the combined strategy. Global clinical efficacy was rated good or very good in 69% of patients in group A and 88% in group B, while lesion clearance rates were 56% and 82%, respectively. Tolerability was generally good, and no treatment-related adverse events were formally recorded. In the imaging substudy, significant reductions in epidermal and stratum corneum thickness occurred only in group B.

Conclusions: Oral retinol combined with medical photoprotection was associated with earlier and greater improvements than oral retinol alone or standard photoprotection recommendations. These findings support further controlled studies to confirm efficacy and clarify the contribution of each intervention.

Trial registration: Trial registration number ISRCTN42565762, retrospectively registered on 18 May 2026.

口服视黄醇单独或联合医用光防护治疗光化性角化患者:一项随机、开放标签、前瞻性、多中心研究
光化性角化病(AK)是一种慢性紫外线诱导的疾病,有可能发展为鳞状细胞癌。本研究评估了口服视黄醇单独或联合含有吡罗西康的广谱医用光保护对轻度至中度AK患者的疗效和耐受性。方法:在这项多中心、前瞻性、随机、开放标签的研究中,117例患有最多6个AK病变的患者被分配到口服视黄醇50,000国际单位(IU)/天(A组)、口服视黄醇加药物光保护(B组)或标准光保护建议(C组)。治疗6个月,随访3个月。在基线和第3、6、9个月进行评估。主要终点是光化性角化面积和严重程度指数(AKASI)的变化。次要结果包括总体临床疗效、病变清除率、耐受性和探索性线场共聚焦光学相干断层扫描结果。结果:117例患者均纳入意向治疗分析,99例纳入方案分析。A组患者AKASI评分在第6个月显著下降- 19.3%(平均差值(MD) 0.61, 95%可信区间(CI) 0.11-1.11;p结论:口服视黄醇联合医用光保护比单独口服视黄醇或标准光保护建议更早和更大的改善。这些发现支持进一步的对照研究,以确认疗效并阐明每种干预措施的作用。试验注册:试验注册号为ISRCTN42565762,回顾性注册于2026年5月18日。
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来源期刊
Dermatology and Therapy
Dermatology and Therapy Medicine-Dermatology
CiteScore
6.00
自引率
8.80%
发文量
187
审稿时长
6 weeks
期刊介绍: Dermatology and Therapy is an international, open access, peer-reviewed, rapid publication journal (peer review in 2 weeks, published 3–4 weeks from acceptance). The journal is dedicated to the publication of high-quality clinical (all phases), observational, real-world, and health outcomes research around the discovery, development, and use of dermatological therapies. Studies relating to diagnosis, pharmacoeconomics, public health and epidemiology, quality of life, and patient care, management, and education are also encouraged. Areas of focus include, but are not limited to all clinical aspects of dermatology, such as skin pharmacology; skin development and aging; prevention, diagnosis, and management of skin disorders and melanomas; research into dermal structures and pathology; and all areas of aesthetic dermatology, including skin maintenance, dermatological surgery, and lasers. The journal is of interest to a broad audience of pharmaceutical and healthcare professionals and publishes original research, reviews, case reports/case series, trial protocols, and short communications. Dermatology and Therapy will consider all scientifically sound research be it positive, confirmatory or negative data. Submissions are welcomed whether they relate to an International and/or a country-specific audience, something that is crucially important when researchers are trying to target more specific patient populations. This inclusive approach allows the journal to assist in the dissemination of quality research, which may be considered of insufficient interest by other journals. The journal appeals to a global audience and receives submissions from all over the world.
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