钙泊三醇和 5-氟尿嘧啶联合疗法用于治疗临床上的日光性角化病:综述文章。

IF 2.9 3区 医学 Q2 PHARMACOLOGY & PHARMACY
Clinical Drug Investigation Pub Date : 2024-10-01 Epub Date: 2024-09-28 DOI:10.1007/s40261-024-01392-w
Anna H Dlott, Sara A Spencer, Anthony J Di Pasqua
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引用次数: 0

摘要

本综述探讨了 5-氟尿嘧啶(5-FU)和钙泊三醇联合治疗光化性角化病的药理、疗效和安全性、剂量和用法以及在治疗中的地位。目前,5% 5-FU 外用乳膏已被批准用于治疗光化性角化病,而钙泊三醇则适用于成人斑块状银屑病。5-FU 的典型用法是每天两次局部涂抹,最长持续 4 周;而钙泊三醇则是在医生指导下每天涂抹一到两次薄层。5-FU 的不良反应主要是局部的,包括皮肤刺激、溃疡、瘙痒、红斑、结痂和湿疹反应,因为全身吸收极少。钙泊三醇可能会引起烧灼感、瘙痒和皮肤过敏。本综述详细介绍了研究将局部 5-FU 与钙泊三醇联合用于治疗光化性角化病这一创新方法的临床试验,并重点介绍了其显著疗效。值得注意的是,临床试验表明,所有参与者的皮损面积都有所缩小或完全清除,对治疗成功的不良影响极小。5-FU 和钙泊三醇的组合能增强免疫反应,针对细胞过度生长,从而有效治疗光化性角化病,同时减少局部反应,缩短现有疗法通常需要的漫长治疗时间。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Calcipotriol and 5-Fluorouracil Combination Therapy for the Treatment of Actinic Keratosis in the Clinic: A Review Article.

This review examines the pharmacology, efficacy and safety, dosage and administration, and place in therapy of the combination of 5-fluorouracil (5-FU) and calcipotriol for the treatment of actinic keratosis. Currently, 5% 5-FU topical cream is approved for actinic keratosis treatment, while calcipotriol is indicated for plaque psoriasis in adults. The typical administration of 5-FU involves topical application twice daily for up to 4 weeks, whereas calcipotriol is applied in a thin layer once or twice daily as directed by a physician. Adverse effects of 5-FU are primarily localized, including skin irritation, ulceration, pruritus, erythema, crusting, and eczematous reactions due to minimal systemic absorption. Calcipotriol may cause burning, itching, and skin irritation. This review details clinical trials that investigate the innovative approach of combining topical 5-FU with calcipotriol for actinic keratosis treatment, highlighting the significant outcomes. Notably, the clinical trials indicate that all participants experienced either a reduction in lesion size or complete lesion clearance, with minimal adverse effects impacting treatment success. The combination of 5-FU and calcipotriol effectively treats actinic keratosis by enhancing the immune response and targeting cell overgrowth, while reducing local site reactions and the lengthy treatment time often associated with existing therapies.

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来源期刊
CiteScore
5.90
自引率
3.10%
发文量
108
审稿时长
6-12 weeks
期刊介绍: Clinical Drug Investigation provides rapid publication of original research covering all phases of clinical drug development and therapeutic use of drugs. The Journal includes: -Clinical trials, outcomes research, clinical pharmacoeconomic studies and pharmacoepidemiology studies with a strong link to optimum prescribing practice for a drug or group of drugs. -Clinical pharmacodynamic and clinical pharmacokinetic studies with a strong link to clinical practice. -Pharmacodynamic and pharmacokinetic studies in healthy volunteers in which significant implications for clinical prescribing are discussed. -Studies focusing on the application of drug delivery technology in healthcare. -Short communications and case study reports that meet the above criteria will also be considered. Additional digital features (including animated abstracts, video abstracts, slide decks, audio slides, instructional videos, infographics, podcasts and animations) can be published with articles; these are designed to increase the visibility, readership and educational value of the journal’s content. In addition, articles published in Clinical Drug Investigation may be accompanied by plain language summaries to assist readers who have some knowledge, but non in-depth expertise in, the area to understand important medical advances.
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