A Study Comparing Cancer Imaging Approaches in People With Lobular Breast Cancer
18F-Fluoroestradiol (FES) Positron Emission Tomography for the Detection and Treatment Response Monitoring in Patients With Metastatic Lobular Breast Carcinoma
Memorial Sloan Kettering Cancer Center
30 participants
Aug 13, 2024
OBSERVATIONAL
Conditions
Summary
The purpose of this study to compare two types of cancer imaging scans to see which is better at detecting and monitoring metastatic ILC. This study will compare PET/CT (positron emission tomography/computed tomography) scans using the radiotracer fluorine 18 (18F)-fluoroestradiol (FES) with a standard imaging approach for detecting and monitoring ILC, PET/CT scans using the radiotracer 18F-fluorodeoxyglucose (FDG). These scans will be referred to as FES PET/CT scans and FDG PET/CT scans.
Eligibility
Inclusion Criteria7
- Adult patient \> 18 years old
- Biopsy-proven metastatic ILC
- Confirmed ER+ breast cancer from either primary tumor or metastatic biopsy (ER receptor percent staining ≥ 10% of tumor cells by IHC)
- HER2-negative per ASCO/CAP
- ECOG Performance Status Score of 0, 1 or 2.
- Patient can have received up to 2 lines of therapy in the metastatic setting
- Life expectancy of at least 12 months
Exclusion Criteria4
- Low ER expression defined as ER \<10% of tumor cells by IHC
- Patients who have been on adjuvant ER-blocking endocrine therapy with SERM or SERD without an 8- and 24-weeks washout, respectively. (The use of aromatase inhibitors or ovarian suppression is permitted given that they do not block estrogen receptors).
- Pregnancy or lactation or parturient or nursing mother
- Patient presents with any other clinically active, serious, life-threatening disease, medical, or psychiatric condition, and/or who has a life expectancy of \<12 months, or for whom study participation may compromise their management; and/or a patient who the investigator judges to be unsuitable for participation in the study for any reason.
Interventions
Scanned at baseline and again posttreatment within 2 weeks of the restaging FDG PET/CT
Locations(7)
View Full Details on ClinicalTrials.gov
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NCT06557148