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Update on 18 F-Fluoroestradiol.

Authors :
O'Brien SR
Edmonds CE
Ward RE
Taunk NK
Pantel AR
Mankoff DA
Source :
Seminars in nuclear medicine [Semin Nucl Med] 2024 Nov; Vol. 54 (6), pp. 812-826. Date of Electronic Publication: 2024 Oct 05.
Publication Year :
2024

Abstract

<superscript>18</superscript> F-16α-Fluoroestradiol ( <superscript>18</superscript> F-FES) is a radiolabeled estrogen analogue positron emission tomography (PET) imaging agent that binds to the estrogen receptor (ER) in the nucleus of ER-expressing cells. Proof-of-concept studies of <superscript>18</superscript> F-FES demonstrated expected correlation between tumoral <superscript>18</superscript> F-FES-positivity on PET-imaging and ER+ status assessed on biopsy samples by radioligand binding and immunohistochemistry. After decades of study, <superscript>18</superscript> F-FES PET/CT gained clinical approval in 2016 in France and 2020 in the United States for use in patients with ER+ metastatic or recurrent breast cancer. ER+ as assessed by <superscript>18</superscript> F-FES PET/CT has been shown to serve as a biomarker, identifying metastatic breast cancer patients who may respond to endocrine therapy and those who are unlikely to respond. In 2023, the Society of Nuclear Medicine and Molecular Imaging (SNMMI) published Appropriate Use Criteria for <superscript>18</superscript> F-FES PET/CT, identifying four indications in which use of <superscript>18</superscript> F-FES PET/CT was "appropriate": (1) To assess functional ER status in metastatic lesions unfavorable to biopsy or when biopsy is nondiagnostic, (2) To detect ER status when other imaging tests are equivocal or suspicious, and at (3) initial diagnosis of metastatic disease or (4) progression of metastatic disease, for considering endocrine therapy. This article reviews the foundations of <superscript>18</superscript> F-FES imaging, including normal distribution, false positives, and false negatives, and describes the most up-to-date clinical uses as well as emerging research in breast cancer and other patient populations.<br />Competing Interests: Declaration of competing interest The authors declare the following financial interests/personal relationships which may be considered as potential competing interests: Sophia O'Brien reports a relationship with GE that includes: consulting or advisory. Austin Pantel reports a relationship with GE that includes: consulting or advisory. David Mankoff reports a relationship with GE that includes: consulting or advisory. Neil Taunk reports a relationship with Boston Scientific, Point Biopharma, Novartis, GE Healthcare, Varian Medical Systems that includes: consulting or advisory. If there are other authors, they declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper. Sophia O'Brien, Austin Pantel, Christine Edmonds, and David Mankoff are supported by a Komen Scholar Grant (Komen SAC231245)<br /> (Copyright © 2024 Elsevier Inc. All rights reserved.)

Details

Language :
English
ISSN :
1558-4623
Volume :
54
Issue :
6
Database :
MEDLINE
Journal :
Seminars in nuclear medicine
Publication Type :
Academic Journal
Accession number :
39368910
Full Text :
https://doi.org/10.1053/j.semnuclmed.2024.09.001