RecruitingPhase 3NCT06611891
Evaluation of Somatostatin Receptor Expression in PET 68Ga-DOTATOC in Patients Followed for Metastatic Breast Cancer
Sponsor
University Hospital, Grenoble
Enrollment
25 participants
Start Date
Jan 6, 2025
Study Type
INTERVENTIONAL
Conditions
Summary
DOTABREAST: Evaluation of Somatostatin Receptor Expression in PET 68Ga-DOTATOC in Patients Followed for Metastatic Breast Cancer This is a prospective, monocentric, non-controlled, non-randomized, open-label, interventional study.
Eligibility
Sex: FEMALEMin Age: 18 YearsMax Age: 99 Years
Inclusion Criteria9
- Age over 18
- Patients with metastatic breast cancer who have completed at least one first line of systemic therapy for metastatic breast cancer
- Patient labeled on the primary lesion ER+HER2- (20)
- Presence of metastatic liver and bone lesions identifiable with 18F-FDG PET-Scan
- Presence of at least 10 identifiable secondary lesions in 18F-FDG PET-Scan
- No therapeutic change between 18F-FDG PET-Scan and 68Ga-DOTATOC PET-Scan.
- Performing the PET scan with 68Ga-DOTATOC within a maximum of 21 days after the 18F-FDG PET-Scan
- Person affiliated to or benefiting from social security
- Person who has given written informed consent
Exclusion Criteria7
- Patients followed or with history of other active neoplastic pathology (including neuroendocrine tumor)
- Known allergy to 68Ga-DOTATOC or its excipients
- Subject refusing to sign the consent to participate
- Minor subject
- Subject excluded from another study
- Persons referred to Articles L1121-5 to L1121-8 of the Public Health Code (CSP)
- Subject cannot be contacted in case of emergency
Interventions
DRUG68Ga-DOTATOC
Slow direct intravenous injection
Locations(1)
View Full Details on ClinicalTrials.gov
For the most up-to-date information, visit the official listing.
NCT06611891
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