Fasolino Giuseppe, Awada Gil, Moschetta Laura, Koulalis Jorgos Socrates, Neyns Bart, Verhelst Bert, Van Elderen Peter, Nelis Pieter, de Lichtbuer Paul Cardon, Cools Wilfried, Ten Tusscher Marcellinus
Ophthalmology Department, Universitair Ziekenhuis Brussel, 1090 Brussels, Belgium.
J Clin Med. 2023 Feb 3;12(3):1214. doi: 10.3390/jcm12031214.
In the last two decades, an increasing number of so-called molecular-targeted therapies have become available for the treatment of patients with advanced malignancies. These drugs have included inhibitors of proteins in the MAPK pathway, such as BRAF and MEK inhibitors, which are characterized by a distinct toxicity profile. The eye is particularly susceptible to adverse effects due to MEK inhibitors, and the term MEKAR (MEK-inhibitor-associated retinopathy) indicates the presence of subretinal fluid, mimicking central serous chorioretinopathy (CSC). The pathogenesis of the retinal alterations related to MAPK pathway inhibitors is still unclear, and questions are still open. The present study aims to assess the presence of retinal pigment epithelium alterations as predictive parameters for retinal toxicity, analyzing, at the same time, the chorioretinal vascular network in patients undergoing BRAF/MEK inhibitor treatment for different malignancies.
在过去二十年中,越来越多的所谓分子靶向疗法可用于治疗晚期恶性肿瘤患者。这些药物包括MAPK通路中蛋白质的抑制剂,如BRAF和MEK抑制剂,其具有独特的毒性特征。眼睛对MEK抑制剂的不良反应尤为敏感,术语MEKAR(MEK抑制剂相关视网膜病变)表示存在视网膜下液,类似于中心性浆液性脉络膜视网膜病变(CSC)。与MAPK通路抑制剂相关的视网膜改变的发病机制仍不清楚,问题仍然存在。本研究旨在评估视网膜色素上皮改变作为视网膜毒性预测参数的存在情况,同时分析接受BRAF/MEK抑制剂治疗不同恶性肿瘤的患者的脉络膜视网膜血管网络。