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Clinical Trials in Canada / NCT01990521
Active, not recruiting Not applicable

Prostate Screening Study Using MRI in BRCA Carriers

NCT01990521 · tracked via the Priya Life Science Canada tracker
Sponsor
Toronto Sunnybrook Regional Cancer Centre
Phase
Not applicable
Started
2014-01
Last updated
2025-09-09

Condition(s) studied

Prostate Cancer

Investigational drug(s) / intervention(s)

MS3TMRI / TRUS Guided BiopsyMS3TMRI / TRUS Guided Biopsy

MS3TMRI / TRUS Guided Biopsy: Patients would undergo MS3TMRI and then have a transrectal ultrasound (TRUS) biopsy performed within one month after the MRI. The initial cores would be obtained using TRUS without MRI information (TRUSBx). During the same biopsy session, the MS3TMRI information would be given to the physician performing the biopsy and additional cores specifically targeted to suspicious areas would be performed (MS3TMRI-TRUSBx).

MS3TMRI / TRUS Guided Biopsy: Multispectral 3T MRI (MS3TMRI) is a device that uses a 3T MRI system without an endorectal receiver coil and with a surface phased array coil. 3T MRI in addition to established computer aided diagnosis (CAD) has been used to perform guided biopsies in an active surveillance population and demonstrated a positive predictive value and negative predictive value of 83% and 81%. A recently completed a study looking at repeat prostate biopsies in men followed on an active surveillance population at Sunnybrook has shown that the PPV of MS3TMRI guided biopsy to be 85%, while the negative predictive value was 100% (Haider, Vesprini and Milot, unpublished).

Study summary

Men with a BRCA1 or BRCA2 mutation are at increased risk for early onset, aggressive prostate cancer compared to men in the general population.

Standard of care screening for men with a BRCA mutation includes PSA testing and digital rectal examination (DRE), the same as with men in the general population.

This study is being done to assess whether there is value in using MRI as a screening tool to detect prostate cancer at an earlier stage than may otherwise be detected using standard of care screening (PSA, DRE). It is unclear whether MRI has utility as a screening tool in this specific population at high risk for aggressive disease.

Eligibility

Sex
MALE
Min age
50 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Enrolled in the Male Hereditary Cancer Research Program at Sunnybrook Health Sciences Center. * Have positive genetic testing for a pathogenic BRCA1 or BRCA2 mutation. * Clinically eligible for and willing to undergo ultrasound biopsy within 4 weeks after the MRI. * Be 50 years of age or older. Exclusion Criteria: * Claustrophobia * Contraindication to MRI * Contraindication to receiving low molecular weight MRI contrast agent * Previously diagnosed with prostate cancer

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Sunnybrook Odette Cancer Centre Toronto Ontario

More Toronto Sunnybrook Regional Cancer Centre trials in Canada

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT01990521 on ClinicalTrials.gov ↗ ← All trials in Canada