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 asses'/> 18F-Fluoroestradiol PET: Current Status and Potential Future Clinical Applications
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18F-Fluoroestradiol PET: Current Status and Potential Future Clinical Applications

机译:18F-氟雌二醇PET:现状和潜在的未来临床应用

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id="p-5">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 18F-fluoroestradiol (18F-FES) PET. Clinical studies have demonstrated the use of 18F-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 18F-FES, highlights the current experience with 18F-FES in patient studies on breast cancer and other diseases, and discusses potential clinical applications and the possible future clinical use of 18F-FES PET.
机译:id =“ p-5”>乳腺癌中的雌激素受体(ER)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。然而,最近的进展允许使用 18 F-氟雌二醇( 18 F-FES)PET体内评估ER表达。临床研究证明了 18 F-FES PET作为定量体内ER表达的方法的用途,并探索了其作为预测性测定方法和评估对内分泌疗法的体内药效学反应的方法的潜力。这篇综述概述了 18 F-FES的生物学和药代动力学,重点介绍了 18 F-FES在乳腺癌和其他疾病的患者研究中的最新经验,并讨论了潜在的临床应用 18 F-FES PET的应用和未来的临床应用。

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