Evaluation of Somatostatin Receptor Expression in PET 68Ga-DOTATOC in Patients Followed for Metastatic Breast Cancer

Status: Recruiting
Location: See location...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Phase 3
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
Participation Requirements
Sex: Female
Minimum Age: 18
Maximum Age: 99
Healthy Volunteers: f
View:

• 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

Locations
Other Locations
France
CHU Grenoble Alpes
RECRUITING
Grenoble
Contact Information
Primary
Marine FAURE
MFaure6@chu-grenoble.fr
0476766872
Backup
Pierre PITTET
ppittet@chu-grenoble.fr
0476766872
Time Frame
Start Date: 2025-01-06
Estimated Completion Date: 2026-10
Participants
Target number of participants: 25
Treatments
Experimental: Performing a 68Ga-Dotatoc PET scan in patients followed for metastatic breast cancer.
1. Prescreening of the patient followed for metastatic breast cancer during the routine care~2. V1 Selection: Patient's selection in the Nuclear Medicin or Oncology department~3. V2 Inclusion: The day of the 68Ga-Dotatoc PET scan in the Nuclear Medicin department~4. V3 End of study visit, the same day after the 68Ga-Dotatoc PET scan.
Related Therapeutic Areas
Sponsors
Leads: University Hospital, Grenoble

This content was sourced from clinicaltrials.gov