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)

CHU Grenoble Alpes

Grenoble, France

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NCT06611891


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