Cognitive Fusion Prostate Biopsy With Biparametric Magnetic Resonance in the Detection of Prostate Cancer

Sponsor
José Joaquín Mira (Other)
Overall Status
Recruiting
CT.gov ID
NCT05818631
Collaborator
(none)
300
1
35.1
8.6

Study Details

Study Description

Brief Summary

The goal of this prospective observational study is to evaluate the diagnostic precision of the Biparametric Magnetic Resonance Imaging (bpMRI) in the detection of clinically significant prostate cancer in patients with biochemical suspicion of prostate cancer (Prostate Specific Antigen in blood test > 4 ng/mL) with a normal digital rectal examination and without a biopsy previous to the MRI. Secondary aims are:

  • Determine the validity as a diagnostic test of the first directed transrectal prostatic biopsy (cognitive fusion) versus systematic biopsy of 12 cylinders in patients with suspicious lesions in the bpMRI.

  • Develop a predictive nomogram that permits the reduction of the number of prostatic biopsies performed to patients with a low suspicion of prostate cancer in the bpMRI.

Condition or Disease Intervention/Treatment Phase
  • Diagnostic Test: fusion cognitive prostate biopsy

Detailed Description

In Spain, prostate cancer (PCa) is the most common cancer independently from gender and the third cause of death in man, below lung and colorectal cancer. Incidence and mortality increase progressively as age increases, hence, due to an older population, this is an outstanding sociosanitary concern.

PCa generally is asymptomatic, diagnosis is based on prostate biopsy in man with an elevated Prostate Specific Antigen (PSA) in blood test and/or a pathologic digital rectal examination.

Multiparametric Magnetic Resonance Imaging (MRImp) plays an important role in the diagnosis. It allows the visualization of the tumor, it values its agresitivity (PI-RADS v2 scale), and permits a directed biopsy to the suspicious lesion.

This tecnique is expensive and very uncomfortable for the patient due its duration (40 minutes) and because it uses intravenous (iv) contrast. Due to these reasons, it is difficult to assume by the sanitary system to perform this technique to every patient with PCa suspicion.

Biparametric MRI emerges as an alternative with a new protocol, performed with less image sequences (T2 and diffusion), cheaper, lasting less (just 15 minutes), and without the administration of iv contrast. Thus, this technique is more assumable by a public sanitary system.

Study Design

Study Type:
Observational
Anticipated Enrollment :
300 participants
Observational Model:
Other
Time Perspective:
Prospective
Official Title:
Determine the Validity as a Diagnostic Test of the Transrectal Prostate Biopsy With Cognitive Fusion Through Biparametric Magnetic Resonance in the Detection of Non-palpabe Prostate Cancer
Actual Study Start Date :
Mar 1, 2021
Anticipated Primary Completion Date :
May 1, 2023
Anticipated Study Completion Date :
Feb 1, 2024

Arms and Interventions

Arm Intervention/Treatment
MRI +

PI-RADS 3-5

Diagnostic Test: fusion cognitive prostate biopsy
A standard transrectal prostatic biopsy will be performed to both groups. To the group with suspicious lesions in the MRI (PI-RADS 3-5), an added directed cognitive fusion biopsy will be performed.
Other Names:
  • directed prostate biopsy
  • MRI -

    PI-RADS 1-2

    Outcome Measures

    Primary Outcome Measures

    1. Diagnostic precision of Biparametric Magnetic Resonance Imaging. [1 hour]

      evaluate the diagnostic precision of the Biparametric Magnetic Resonance Imaging (bpMRI) in the detection of clinically significant prostate cancer in patients with biochemical suspicion of prostate cancer (Prostate Specific Antigen in blood test > 4 ng/mL) with a normal digital rectal examination and without a biopsy previous to the MRI

    Secondary Outcome Measures

    1. Validity of first directed transrectal prostatic biopsy [1 hour]

      Determine the validity as a diagnostic test of the first directed transrectal prostatic biopsy (cognitive fusion) versus systematic biopsy of 12 cylinders in patients with suspicious lesions in the bpMRI.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years to 80 Years
    Sexes Eligible for Study:
    Male
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Male patients between 18 and 80 years

    • BpMRI performed in a 3 months period before the prostatic biopsy

    • First transrectal prostatic biopsy

    • PSA > 4 ng/mL and < 20 ng/mL

    • Patients acceptance to participate in the study signing a written specific informed consent

    Exclusion Criteria:
    • Not having all the inclusion criteria described

    • Suspicious digital rectal examination of prostate cancer

    • Previous urinary tract infection in the last six months, acute urinary retention or being a chronic carrier of bladder catheter

    • Previous prostatic surgery in any of its variants

    • Concomitant treatment with LH-RH analogue, antiandrogens or 5-alfa-reductase inhibitors

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Universidad Miguel Hernández de Elche Alicante Spain 03550

    Sponsors and Collaborators

    • José Joaquín Mira

    Investigators

    None specified.

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    José Joaquín Mira, Director, Universidad Miguel Hernandez de Elche
    ClinicalTrials.gov Identifier:
    NCT05818631
    Other Study ID Numbers:
    • RM FAST
    First Posted:
    Apr 19, 2023
    Last Update Posted:
    Apr 19, 2023
    Last Verified:
    Apr 1, 2023
    Individual Participant Data (IPD) Sharing Statement:
    Undecided
    Plan to Share IPD:
    Undecided
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Apr 19, 2023