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F-18-Fluoroestradiol PET: Current Status and Potential Future Clinical Applications

机译:F-18-氟雌二醇PET:现状和潜在的未来临床应用

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摘要

Estrogen receptor (ER) expression in breast cancer is associated with a more favorable prognosis and is necessary for a response to endocrine therapies. Traditionally, ER expression is assessed by in vitro assays on biopsied tumor tissue. However, recent advances have allowed in vivo evaluation of ER expression with F-18-fluoroestradiol (F-18-FES) PET. Clinical studies have demonstrated the use of F-18-FES PET as a method for quantifying in vivo ER expression and have explored its potential as a predictive assay and method of assessing in vivo pharmacodynamic response to endocrine therapy. This review outlines the biology and pharmacokinetics of F-18-FES, highlights the current experience with F-18-FES in patient studies on breast cancer and other diseases, and discusses potential clinical applications and the possible future clinical use of F-18-FES PET.
机译:乳腺癌中雌激素受体(ER)的表达与更有利的预后相关,并且是对内分泌疗法作出反应所必需的。传统上,ER的表达是通过活检肿瘤组织的体外测定来评估的。但是,最近的进展允许体内评价F-18-氟雌二醇(F-18-FES)PET的ER表达。临床研究表明,将F-18-FES PET用作定量体内ER表达的方法,并已探索了其作为预测性检测方法和评估体内对内分泌治疗的药效学反应的方法的潜力。这篇综述概述了F-18-FES的生物学和药代动力学,重点介绍了F-18-FES在乳腺癌和其他疾病的患者研究中的最新经验,并讨论了F-18-FES的潜在临床应用和未来可能的临床应用FES PET。

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