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Prostate Screening Study Using MRI in BRCA Carriers

Primary Purpose

Prostate Cancer

Status
Recruiting
Phase
Not Applicable
Locations
Canada
Study Type
Interventional
Intervention
MS3TMRI / TRUS Guided Biopsy
MS3TMRI / TRUS Guided Biopsy
Sponsored by
Toronto Sunnybrook Regional Cancer Centre
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Prostate Cancer

Eligibility Criteria

50 Years - undefined (Adult, Older Adult)MaleDoes not accept healthy volunteers

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

Sites / Locations

  • Sunnybrook Odette Cancer CentreRecruiting

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

MS3TMRI / TRUS Guided Biopsy

Arm Description

Outcomes

Primary Outcome Measures

Prostate MRI in BRCA carriers
Measure of prostate MRI to determine the PPV of MRI for detection of actionable prostate cancer

Secondary Outcome Measures

Prostate cancer in BRCA carriers
Prevalence of any prostate cancer compared to actionable cancer in men with a BRCA1 or BRCA2 mutation independent of serum PSA value.

Full Information

First Posted
November 15, 2013
Last Updated
April 12, 2023
Sponsor
Toronto Sunnybrook Regional Cancer Centre
Collaborators
Sunnybrook Health Sciences Centre, Women's College Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT01990521
Brief Title
Prostate Screening Study Using MRI in BRCA Carriers
Official Title
Screening Male BRCA Mutation Carriers: Effectiveness of Multispectral 3T Magnetic Resonance Imaging
Study Type
Interventional

2. Study Status

Record Verification Date
April 2023
Overall Recruitment Status
Recruiting
Study Start Date
January 2014 (Actual)
Primary Completion Date
December 2024 (Anticipated)
Study Completion Date
January 2025 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Toronto Sunnybrook Regional Cancer Centre
Collaborators
Sunnybrook Health Sciences Centre, Women's College Hospital

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief 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.
Detailed Description
To determine the value of using Multispectral 3T MRI (MS3TMRI) for prostate cancer screening in men with a high risk of developing early onset aggressive prostate cancer given known BRCA1 or BRCA2 mutation carrier status, with no prior prostate cancer diagnosis, independent of baseline PSA levels. Determine the prevalence of prostate cancer in BRCA1 and BRCA2 mutation carriers independent of baseline PSA levels. To evaluate the accuracy of tumor targeting based on MRI and ultrasound (US) tumor co-localization. To evaluate the sensitivity, specificity, PPV, NPV, and accuracy of an automated computer aided diagnosis method (CAD) applied to MS3TMRI in the prediction of zonal biopsy results for the presence or absence of a significant cancer.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Prostate Cancer

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
60 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
MS3TMRI / TRUS Guided Biopsy
Arm Type
Experimental
Intervention Type
Procedure
Intervention Name(s)
MS3TMRI / TRUS Guided Biopsy
Intervention Description
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).
Intervention Type
Device
Intervention Name(s)
MS3TMRI / TRUS Guided Biopsy
Other Intervention Name(s)
Multispectral 3T MRI, Transrectal Ultrasound
Intervention Description
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).
Primary Outcome Measure Information:
Title
Prostate MRI in BRCA carriers
Description
Measure of prostate MRI to determine the PPV of MRI for detection of actionable prostate cancer
Time Frame
2 years (January 2016)
Secondary Outcome Measure Information:
Title
Prostate cancer in BRCA carriers
Description
Prevalence of any prostate cancer compared to actionable cancer in men with a BRCA1 or BRCA2 mutation independent of serum PSA value.
Time Frame
2 years January 2016

10. Eligibility

Sex
Male
Minimum Age & Unit of Time
50 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
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
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Danny J Vesprini, MD, MSc, FRCPC
Phone
416-480-4806
Email
danny.vesprini@sunnybrook.ca
First Name & Middle Initial & Last Name or Official Title & Degree
Justin A Lorentz, MSc, CGC
Phone
416-480-500
Ext
83683
Email
justin.lorentz@sunnybrook.ca
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Danny J Vesprini, MD, MSc, FRCPC
Organizational Affiliation
Sunnybrook Health Sciences Centre
Official's Role
Principal Investigator
Facility Information:
Facility Name
Sunnybrook Odette Cancer Centre
City
Toronto
State/Province
Ontario
ZIP/Postal Code
M4N 3M5
Country
Canada
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Danny J Vesprini, MD, MSc, FRCPC
Phone
416-480-4806
Email
danny.vesprini@sunnybrook.ca
First Name & Middle Initial & Last Name & Degree
Justin A Lorentz, MSc, CGC
Phone
416-480-5000
Ext
83683
Email
justin.lorentz@sunnybrook.ca
First Name & Middle Initial & Last Name & Degree
Justin A Lorentz, MSc, CGC
First Name & Middle Initial & Last Name & Degree
Danny J Vesprini, MD, MSc, FRCPC

12. IPD Sharing Statement

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Prostate Screening Study Using MRI in BRCA Carriers

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