St. Josef-Hospital, Klinikum der Ruhr-Universität Bochum, Bochum, Germany.
Expert Opin Emerg Drugs. 2020 Mar;25(1):49-58. doi: 10.1080/14728214.2020.1730810. Epub 2020 Feb 20.
: Actinic keratosis (AK) is a chronic disease which is mainly located across areas of sun-exposed skin. Clinical and subclinical lesions coexist across a large area resulting in a field cancerization. As these lesions have the potential to transform into invasive squamous cell carcinoma (iSCC), treatment is crucial. With global prevalence increasing, AK is expected to be the most common in situ carcinoma of the skin.: In this article, we cover the established algorithm of treating AK and give an insight into the drugs under development. There are six compounds under development covering different treatment angles, from Sinecatechin a Polyphenon E which targets the link between HPV infection and development of AK, over Tirbanibulin which targets the SRC proto-oncogene and fast proliferating cells, to Tuvatexib a small-molecule dual VDAC/HK2 modulator that has shown that it can compete with the established therapies.: These new treatment options are moving us further toward a more individually tailored treatment for each patient considering his abilities, the size and location of his lesions but also the genetic bases as well as individual risk of transforming into a iSCC and possibly other factors contributing to each patients individual AK lesions.
光化性角化病(AK)是一种主要发生在暴露于阳光的皮肤区域的慢性疾病。临床和亚临床病变广泛共存,导致区域性癌化。由于这些病变有可能转化为侵袭性鳞状细胞癌(iSCC),因此治疗至关重要。随着全球患病率的增加,AK 预计将成为最常见的皮肤原位癌。
在本文中,我们介绍了治疗 AK 的既定方案,并深入探讨了正在开发中的药物。目前有六种化合物正在开发中,涵盖了不同的治疗角度,从针对 HPV 感染与 AK 发展之间联系的 Sinecatechin a Polyphenon E,到针对 SRC 原癌基因和快速增殖细胞的 Tirbanibulin,再到 Tuvatexib 一种小分子双重 VDAC/HK2 调节剂,已证明它可以与现有的治疗方法竞争。
这些新的治疗选择使我们能够根据每位患者的能力、病变的大小和位置以及遗传基础以及转化为 iSCC 的个体风险,以及可能导致每位患者 AK 病变的其他因素,为每位患者制定更个体化的治疗方案。