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Recruiting NCT04732156

Detection of ISUP≥2 Prostate Cancers Using Multiparametric MRI: Prospective Multicenter Comparison of the PI-RADS Score and an Artificial Intelligence System

Trial Parameters

Condition Prostate Cancer
Sponsor Hospices Civils de Lyon
Study Type INTERVENTIONAL
Phase N/A
Enrollment 420
Sex MALE
Min Age 18 Years
Max Age 80 Years
Start Date 2021-04-14
Completion 2026-06-15
Interventions
Blood sampleFollow up questionnaireHuman reading of prostate MR images (PI-RADSv2.1).

Brief Summary

Multiparametric MRI of the prostate is recommended before each prostate biopsy. It identifies suspicious areas which will then be the subject of targeted biopsies. However, MRI suffers from low specificity and moderate inter-reader reproducibility, including with the use of the PI-RADS version 2.1 score. We are developing, within the framework of RHU PERFUSE, a computer-aided diagnosis system (CAD) for the detection of ISUP ≥2 cancers. This system has been trained on a database of patients who had prostate MRI and prostatectomy at the Hospices Civils de Lyon and performed well on a database of patients who had prostate MRI before biopsy at the Hopices civils de Lyon. However, one of the weaknesses of artificial intelligence systems is their low robustness when tested on MRI images from different manufacturers or institutions. The goal of the CHANGE study is to build a prospective multicenter cohort of patients who underwent prostate multiparametric MRI followed by systematic and targeted prostate biopsies. The cohort will be used for the final external validation of the CAD developed in PERFUSE.

Eligibility Criteria

Inclusion Criteria: * Men over 18 years of age * Patient with clinical suspicion of prostate cancer referred for a multiparametric MRI of the prostate before a first series of biopsies or before new biopsies after one or more series of negative biopsies * PSA ≤ 30 ng / ml * Clinical stage ≤ T2c * Affiliation or beneficiary of a social security scheme Exclusion Criteria: * Men over 80 years of age * PSA\> 30 ng / ml * Stage T3 or T4 on digital rectal examination * Previous prostate biopsy performed within 12 months * History of prostate cancer diagnosed by biopsy or endourethral resection. * History of pelvic radiotherapy regardless of the cause. * History of total or focal treatment for prostate cancer. * History of hormone therapy * MRI performed more than 3 months before biopsy * Prostate MRI performed on a machine other than the center's machines accredited for the study. * Presence of a hip prosthesis * Contraindication to performing an MRI * Contraindication to performing prostate

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