Related Experiment Video
Updated: Mar 19, 2026

10:20
Automation of a Positron-emission Tomography PET Radiotracer Synthesis Protocol for Clinical Production
Published on: October 26, 2018
12.0K
18F-Fluoroestradiol PET: Current Status and Potential Future Clinical Applications
Geraldine J Liao1, Amy S Clark2, Erin K Schubert3
1Department of Radiology, Hospital of the University of Pennsylvania, Philadelphia, Pennsylvania.
Summary
Fluorine-18-fluoroestradiol (18F-FES) PET imaging allows in vivo evaluation of estrogen receptor (ER) expression in breast cancer. This technique offers a non-invasive method to assess ER status, predict treatment response, and monitor therapy effectiveness.
Area of Science:
- Nuclear Medicine
- Oncology
- Radiochemistry
Background:
- Estrogen receptor (ER) expression in breast cancer is crucial for prognosis and response to endocrine therapy.
- Traditional ER assessment relies on invasive in vitro assays of tumor biopsies.
- In vivo evaluation of ER expression is now possible with advancements in PET imaging.
Purpose of the Study:
- To review the biology and pharmacokinetics of (18)F-FES.
- To highlight current clinical experiences with (18)F-FES PET in breast cancer and other diseases.
- To discuss the potential clinical applications and future use of (18)F-FES PET.
Main Methods:
- Review of existing literature on (18)F-FES PET imaging.
- Analysis of clinical studies involving (18)F-FES PET in various diseases.
- Discussion of the biological and pharmacokinetic properties of (18)F-FES.
Main Results:
- (18)F-FES PET can quantify in vivo ER expression.
- (18)F-FES PET has shown potential as a predictive assay for treatment response.
- (18)F-FES PET can assess in vivo pharmacodynamic response to endocrine therapy.
Conclusions:
- (18)F-FES PET is a valuable tool for assessing ER status non-invasively.
- This imaging modality holds promise for personalized medicine in breast cancer treatment.
- Further clinical application and validation of (18)F-FES PET are anticipated.
![Radiosynthesis of 1-2-[18F]Fluoroethyl-L-Tryptophan using a One-pot, Two-step Protocol](/_next/image?url=https%3A%2F%2Fcloudfront.jove.com%2FCDNSource%2Fteasers%2F63025.jpg&w=3840&q=50)
![Automated Radiochemical Synthesis of [18F]3F4AP: A Novel PET Tracer for Imaging Demyelinating Diseases](/_next/image?url=https%3A%2F%2Fcloudfront.jove.com%2FCDNSource%2Fteasers%2F55537.jpg&w=3840&q=50)