PSMA-PET/CT to Assess the Expression of Specific Membrane Antigen (PSMA) in Patients With Progressive Triple-negative Breast Cancer.
Recruiting now · Phase 2
Conditions studied: TNBC - Triple-Negative Breast Cancer
In brief
This is a descriptive, prospective, single centre study. This study will assess PSMA expression via the uptake of radiolabelled PSMA-ligand using PET/CT imaging in mTNBC lesions pre-identified on 18F-FDG PET/CT in order to evaluate the feasibility of molecular radionuclide therapy in refractory mTNBC using the Lutetium-177 radiolabelled PSMA.
Key facts
- Study ID
- NCT06059469
- Run by
- Jules Bordet Institute
- People needed
- 20
- Starts
- 2022-05-30
- Expected to finish
- 2025-12-01
- Last updated by the study team
- 2025-07-18
Who can join
Age: 18 and older. Sex: female. Healthy volunteers: not accepted.
You may qualify if…
- Written informed consent in accordance with institutional guidelines and obtained prior to any study procedure
- Women with ≥ 18 years-old
- Eastern Cooperative Oncology Group Performance Status of 0 to 2
- Confirmed diagnosis of progressive metastatic TNBC and presenting measurable disease on 18F-FDG PET/CT (performed within 2 weeks) or Brain MRI in case of progressive brain metastases (performed within 4 weeks) prior to PSMA PET/CT.
- Radiolabelled PSMA PET/CT has to be performed before the next treatment line initiation
You may not qualify if…
- Pregnant or lactating patients
- Other active neoplastic disease
- Treatment by another molecule that is the object of investigation within 30 days
- Skin only metastatic disease
- Patients with a significant medical, neuro-psychiatric, or surgical condition, which, in the investigator's opinion, may interfere with completion of the study
Where it is running
- Institut Jules Bordet — Brussels, Belgium (enrolling)
Full record on ClinicalTrials.gov
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