Clinical Trial · NCT07370597

LUtetium-177 DOsimetry as a Predictive Biomarker of Response in Metastatic Prostate Cancer Patients Treated With PSMA Radioligand THerapy.

Overview

If dosimetry calculations could predict which patients would ultimately respond or not respond to treatment, administered dose and number of 177Lu-PSMA-RLT cycles could be adapted early during the treatment course. In this context, our study aims to analyze if absorbed tumour dose obtained by dosimetry calculations could be used as a biomarker to predict non-response to treatment early after one cycle, as the first step towards treatment dose adaptation of a personalized radionuclide treatment approach.

Sponsor

Jules Bordet Institute

Phase

N/A

Contacts

Carlos Artigas, MD

carlos.artigas@hubruxelles.be

02.54137.81

ClinicalTrials.gov

NCT07370597

Drug / Compound

177Lu-PSMA

Isotope(s):
Target(s):
  • PSMA