Tirbanibulin 1% Ointment: The Mechanism of Action of a Novel Topical Therapy for Actinic Keratosis.

IF 1.8 4区 医学 Q3 DERMATOLOGY
Alyssa M Roberts, Leon Kircik, Mark Lebwohl, April W Armstrong
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引用次数: 0

Abstract

Actinic keratosis (AK) is a common, precancerous skin lesion that may progress to squamous cell carcinoma (SCC). Traditional topical therapies for AKs often require long treatment durations. These therapies may also cause significant local skin reactions that can reduce patient adherence. Tirbanibulin, a first-in-class topical agent for AKs on the face and scalp, was approved by the US Food and Drug Administration (FDA) in 2020. Tirbanibulin serves as a promising alternative with a shorter treatment duration of five days. Unlike other topical AK therapies, tirbanibulin targets microtubules in keratinocytes. The agent inhibits tubulin polymerization, disrupts the microtubule network, and induces cell cycle arrest. These cellular effects may be reversible, reducing tirbanibulin's toxicity profile. Tirbanibulin has also demonstrated antiproliferative activity with the potential to selectively target highly proliferative keratinocytes, contributing to its antitumorigenic effects. In addition, studies suggest that tirbanibulin may induce apoptosis and interfere with the activity of Src, a tyrosine kinase that can contribute to the progression of AKs and SCCs. Tirbanibulin’s shorter treatment duration and favorable safety profile make it an appealing choice in AK management. In clinical studies, tirbanibulin 1% ointment was well-tolerated and demonstrated significant efficacy in clearing AK lesions in areas up to 100 cm2 on the face and scalp. Tirbanibulin's novel mechanism of action introduces a new, exciting option for the field treatment of AKs. J Drugs Dermatol. 2025;24:7(Suppl 1):s13-18.

1%替巴布林软膏:一种新的局部治疗光化性角化病的作用机制。
光化性角化病(AK)是一种常见的癌前皮肤病变,可发展为鳞状细胞癌(SCC)。传统的局部治疗AKs通常需要较长的治疗时间。这些疗法也可能引起明显的局部皮肤反应,从而降低患者的依从性。蒂巴尼布林是一种用于面部和头皮ak的一流外用药物,于2020年获得美国食品和药物管理局(FDA)的批准。蒂巴尼布林是一种有希望的替代方案,治疗时间较短,为5天。与其他局部AK疗法不同,替巴布蛋白靶向角化细胞中的微管。该制剂抑制微管蛋白聚合,破坏微管网络,诱导细胞周期阻滞。这些细胞效应可能是可逆的,从而降低了替巴布林的毒性。蒂巴尼布林也被证明具有抗增殖活性,有可能选择性地靶向高度增殖的角质形成细胞,这有助于其抗肿瘤作用。此外,研究表明,替巴布林可能诱导细胞凋亡并干扰Src的活性,Src是一种酪氨酸激酶,可促进AKs和SCCs的进展。替布林治疗时间短,安全性好,是治疗AK的理想选择。在临床研究中,1%替巴布林软膏耐受性良好,在清除面部和头皮面积达100平方厘米的AK病变方面表现出显著的疗效。蒂巴尼布林的新作用机制为ak的现场治疗提供了一个新的、令人兴奋的选择。皮肤医学杂志,2025;24:7(增刊1):13-18。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
2.20
自引率
13.30%
发文量
289
审稿时长
3-6 weeks
期刊介绍: The Journal of Drugs in Dermatology (JDD) is a peer-reviewed publication indexed with MEDLINE®/PubMed® that was founded by the renowned Dr. Perry Robins MD. Founded in 2002, it offers one of the fastest routes to disseminate dermatologic information and is considered the fastest growing publication in dermatology. We present original articles, award-winning case reports, and timely features pertaining to new methods, techniques, drug therapy, and devices in dermatology that provide readers with peer reviewed content of the utmost quality. Our high standards of content are maintained through a balanced, peer-review process. Articles are reviewed by an International Editorial Board of over 160 renowned experts.
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