Clinical Trials Directory

Trials / Completed

CompletedNCT06919159

Intratumoral Heterogeneity on [18F]PSMA and [18F]FDG PET/CT in Predicting Invasion and Prognosis of Prostate Cancer

Intratumoral Heterogeneity on [18F]PSMA-1007 and [18F]FDG PET/CT in Predicting Invasion and Prognosis of Primary Prostate Cancer

Status
Completed
Phase
Study type
Observational
Enrollment
45 (actual)
Sponsor
Jiequn Yu · Academic / Other
Sex
Male
Age
18 Years
Healthy volunteers

Summary

The purpose of this study is to analyze heterogeneity of prostate cancer(PCa)based on the head-to-head imaging of prostate-specific membrane antigen (PSMA) and fluorodeoxyglucose (FDG) positron emission tomography computed tomography (PET/CT)

Detailed description

PET/CT examinations were performed on different days using Siemens Biograph MCT PET/CT equipment. All patients were examined on the same scanner. Patients were fasted for more than 6 h before \[18F\]FDG PET/CT examination, blood glucose was controlled below 11.1 mmol/L, \[18F\]FDG injection dose was 3.7 MBq/kg, and \[18F\]FDG PET/CT examination was performed after 60 min rest. \[18F\]PSMA-1007 injection dose was 3.7 MBq/kg, and PET/CT scan was performed 60 min after injection. To avoid interference of prostate lesion detection by active urine in the bladder, patients were asked to urinate or undergo forced diuresis before the start of the examination. The scan was performed from the top of the head to the base of the thighs. Low-dose CT was taken with automatic milliampere-second 120 kV voltage scans with a matrix of 512 × 512 and a thickness of 5 mm, and PET/CT image acquisition was taken from 5-6 beds for 2-3 min each. CT data was used for attenuation correction at the end of the acquisition, reconstructed by the two-iteration method (21 subsets in total), and the True X +TOF algorithm was applied to reconstruct the images. Two nuclear medicine physicians with extensive experience in PET/CT interpretation evaluated the images using the LIFEx software v 7.1.0. Both readers were blinded to both clinical and pathological data

Conditions

Interventions

TypeNameDescription
DIAGNOSTIC_TESTPSMA PET/CT scanDifferent developing agents
DIAGNOSTIC_TESTFDG-PETDifferent developing agents

Timeline

Start date
2021-07-01
Primary completion
2022-11-20
Completion
2022-11-30
First posted
2025-04-09
Last updated
2025-04-11

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT06919159. Inclusion in this directory is not an endorsement.