Randomized Prospective Multi Center Cohort Study for Primary Diagnosis of Clinically Significant Prostate Cancer With Combination of PSA/DRE and Multi Parametric Magnetic Resonance Imaging

NANot yet recruitingINTERVENTIONAL
Enrollment

1,908

Participants

Timeline

Start Date

April 1, 2026

Primary Completion Date

March 31, 2030

Study Completion Date

March 31, 2030

Conditions
Prostate Cancer
Interventions
DIAGNOSTIC_TEST

PSA test

testing for blood levels of PSA

DEVICE

multiparametric prostate Magnetic Resonance Imaging (mpMRI)

mpMRI acquisition and reporting will be performed according to the current version of the Prostate Imaging-Reporting and Data System (PI-RADS). MpMRI will be performed at the different study centers on a 3 Tesla MR scanner using multi-phased array surface coil. MpMRI includes T1-weighted and T2-weighted imaging (T1WI, T2WI), diffusion-weighted imaging (DWI), and dynamic contrast-enhanced imaging (DCE-MRI). Hyoscine butyl bromide will be administered to optimize image quality. Prostate imaging quality will be assessed by the prostate imaging quality score (PI-QUAL). In case of contraindications to MRI contrast agents, DCE will be omitted. In case of contraindications to hyoscine butyl bromide, it will be omitted. Lesions with a PI-RADS score of ≥ 4 and 3 with PSAD \> 0.15 will considered suspicious for csPCa.

PROCEDURE

targeted MRI/US fusion-guided biopsy

Targeted MRI/US fusion-guided biopsy (TB) are performed using transrectal ultrasound (max. 4 cores from 3 targets). MRI/US fusion-guided biopsies can be performed transrectally or transperineally. Ultrasound-guided biopsies will be performed with a 3-D probe and with local or general anesthesia. Coverage with antibiotics has to be provided as per local standard of care for all biopsies.

PROCEDURE

combined prostate biopsy (systematic biopsy plus targeted MRI/US fusion-guided biopsy)

The combined biopsy comprises systematic biopsy (SB) and targeted MRI/US fusion-guided biopsy (TB). They are performed using transrectal ultrasound (number of cores: SB 12 cores, TB max. 4 cores from 3 targets). MRI/US fusion-guided biopsies can be performed transrectally or transperineally. Ultrasound-guided biopsies will be performed with a 3-D probe and with local or general anesthesia. Coverage with antibiotics has to be provided as per local standard of care for all biopsies.

PROCEDURE

MRI inbore biopsy

MRI inbore biopsies will be offered after negative initial MRI/US fusion-guided biopsy or diagnosis of only clinically insignificant PCa in initial biopsy in arms A or B. Before performing MRI inbore biopsy the PI-RADS scoring will be re-confirmed. The number of cores will be 2 per target. In case of inaccurate needle position additional cores are allowed to ensure correct targeting. Needle position will be verified in 2 planes. Coverage with antibiotics has to be provided as per local standard of care.

All Listed Sponsors
collaborator

University Hospital, Aachen

OTHER

collaborator

University Hospital, Bonn

OTHER

collaborator

University Hospital of Cologne

OTHER

collaborator

University Hospital, Essen

OTHER

collaborator

University Hospital Muenster

OTHER

collaborator

German Cancer Research Center

OTHER

collaborator

Marienhospital Herne

OTHER

collaborator

Städtische Kliniken Mönchengladbach

UNKNOWN

collaborator

Evangelische Kliniken Essen-Mitte

UNKNOWN

collaborator

Klinikum Dortmund

UNKNOWN

collaborator

Stiftungsklinikum PROSELIS gGmbH Recklinghausen

UNKNOWN

lead

Heinrich-Heine University, Duesseldorf

OTHER