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Clinical Trial · NCT04824014
Overview
This proposed project will focus on 3 specific aims: Compare and complement 4FMFES-PET with FDG-PET and conventional imaging modalities, and evaluate how they improved prognosis and staging of ER+ advanced breast cancer patients; Correlate 4FMFES/FDG uptake and staging with pathological data (histology, receptor status, grade), including distal biopsy metastases sampling; Correlate 4FMFES/FDG uptake and staging with longitudinal outcomes (treatment response, progression-free survival, time-to-relapse) to determine which cohort of patient benefit most from 4FMFES.
Sponsor
Centre de recherche du Centre hospitalier universitaire de Sherbrooke
Phase
Phase 2
Contacts
Michel Paquette, PhD (Principal Investigator)
michel.paquette@usherbrooke.ca
819-346-1110 ext 11-982
Stéphanie Dubreuil
stephanie.dubreuil2@usherbrooke.ca
819-346-1110 ext 16617
ClinicalTrials.gov
NCT04824014Drug / Compound
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