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Clinical Trial · NCT07643935
Overview
177Lutetium-PSMA-617 is an established treatment for patients with metastatic castration-resistant prostate cancer (mCRPC). Early response assessment is critical for optimizing patient management. Response Evaluation Criteria in Prostate Imaging (RECIP) 1.0, initially developed for Positon Emission Tomography (PET) with 68Ga-PSMA, have demonstrated prognostic value, particularly after two treatment cycles. Recent studies suggest that SPECT at cycle 2 provides prognostic information, although it reflects only the first treatment cycle, whereas PET-based RECIP, assessed after cycle 2, captures the effect of two cycles. This study aims to evaluate the prognostic value of quantitative 177Lu-PSMA-SPECT biomarkers and determine the optimal timing for RECIP-based assessment.
Sponsor
Central Hospital, Nancy, France
Contacts
Veronique Roch, MSc (CONTACT)
v.roch@chru-nancy.fr
0383154276
Laetitia IMBERT, PhD (CONTACT)
l.imbert@chru-nancy.fr
0383157879
ClinicalTrials.gov
NCT07643935Drug / Compound
Eligibility
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