Fred Hutch/University of Washington Cancer Consortium
Seattle, Washington, 98109, United States
NCT Number: NCT04692103
This clinical trial studies use of F-18 16 alpha-fluoroestradiol ([F-18] FES) positron emission tomography (PET)/computed tomography (CT) in measuring tumor hormone receptor expression in patients undergoing endocrine-targeted therapy for newly diagnosed breast cancer or breast cancer that has come back or spread to other places in the body. Comparing results of diagnostic procedures done before, during, and after hormone therapy may help measure a patient's response to treatment.
This study is active but is not currently recruiting participants.
Notify Me18 year and older
All sexes
Interventional
Phase 2
Seattle, Washington, 98109, United States
OUTLINE:
Patients undergo F-18 FES PET/CT scan at baseline. Patients also undergo F-18 FES PET/CT and FDG PET/CT between 1-12 weeks after starting therapy, and then 1-12 weeks after the second FES PET/CT scan. Repeat FDG PET may be omitted in patients on selective estrogen receptor degrader.
After completion of study, patients are followed up for up to 20 years.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Undergo F-18 FES PET/CT
Other names: F-18 FES, FES, Fluorine-18 16 alpha-fluoroestradiol, Fluoroestradiol F-18
Undergo F-18 FES PET/CT
Other names: Medical Imaging, PET Scan, Positron Emission Tomography Scan, Positron-Emission Tomography
Undergo F-18 FES PET/CT
Other names: CAT Scan, Computerized Axial Tomography, CT scan
Undergo FDG PET/CT
Other names: FDG, Fluorodeoxyglucose F18, 18FDG
Correlative studies
Time frame: From time of first F-18 FES-PET/CT scan to time of second F-18 FES-PET/CT scan (approximately 1-12 weeks)
FES uptake will be quantified using lean body mass adjusted SUV (SUL). Percentage change in FES average SULmax between baseline and a second FES scan will be calculated for up to 3 lesions per patient.
Time frame: From time of first F-18 FES-PET/CT scan to time of second F-18 FES-PET/CT scan (approximately 1-12 weeks)
Quantitative measures of FES uptake for each disease site will be determined by drawing regions-of-interest on lesions to determine maximal FES uptake (SUVmax) per lesion. Up to 10 sites seen on the static torso survey will be quantified.
Time frame: From time of first F-18 FES-PET/CT scan to time of second F-18 FES-PET/CT scan (approximately 1-12 weeks)
The number of patients showing a 20% increase in FES uptake (SULmean or SUVmax) compared to baseline from the first to second scan using a 90% Wilson score binomial confidence interval.
Time frame: From start of therapy up to 20 years
Time to disease progression will be measured as the time from the start of endocrine therapy to the time the patient is first recorded as having disease progression.
University of Washington
Other
Serial [F-18] Fluoroestradiol (FES) PET Imaging to Evaluate Endocrine-targeted Therapy
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
Published trials that share one or more normalized conditions with this study.
NCT00785291
Breast Diseases, Breast Neoplasms
Scottsdale, Arizona, United States
View Trial DetailsNCT02152943
Advanced Malignant Solid Neoplasm, Breast Diseases
Houston, Texas, United States
View Trial DetailsNCT00390455
Breast Diseases, Breast Neoplasms
Little Rock, Arkansas, United States
View Trial DetailsNCT01344031
Breast Diseases, Breast Neoplasms
St Louis, Missouri, United States
View Trial Details