MR/TRUS Fusion Guided Prostate Biopsy
Primary Purpose
Prostate Disease, Elevated Prostate Specific Antigen, Family History of Prostate Cancer
Status
Unknown status
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
prostate biopsy
MR US Fusion Guided Prostate Biopsy
MR/TRUS Fusion Guided Prostate Biopsy
Sponsored by
About this trial
This is an interventional diagnostic trial for Prostate Disease focused on measuring Targeted Prostate Biopsy
Eligibility Criteria
Inclusion Criteria:
- All patients must have a pre-operative MRI performed in accordance with the MT Sinai/NIH MR prostate imaging guidelines.
- Age greater than 18 years.
- No serious concurrent medical illness that would preclude the patient from making a rational informed decision on participation.
- The ability to understand and willingness to sign a written informed consent form, and to comply with the protocol. If in question, an ethics consult will be obtained.
- Ability to tolerate sedation and or general anesthesia if required.
- PSA >2.5 or Abnormal digital rectal exam or current recommendations for biopsy from the American Urological Association
- Pre-biopsy prostate MRI as described above, showing targetable lesions within 4 months of biopsy
- Able to tolerate a ultrasound guided biopsy
Exclusion Criteria:
- Patients with an altered mental status that precludes understanding or consenting for the biopsy procedure will be excluded from this study.
- Patients unlikely able to hold reasonably still on a procedure table for the length of the procedure.
- Patients with pacemakers or automatic implantable cardiac defibrillators (contraindications to MRI)
- Patients with uncorrectable coagulopathies.
Sites / Locations
- Icahn School of Medicine at Mount SinaiRecruiting
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
Males with Prostate Cancer
Arm Description
Each participant will receive standard of care prostate biopsy as well as a US guided prostate biopsy and a MR/TRUS Fusion Guided prostate biopsy guided prostate biopsy.
Outcomes
Primary Outcome Measures
Incidence of Prostate Cancer
Incidence of diagnosing subjects with prostate cancer with MR visible lesions
Secondary Outcome Measures
Incidence of adverse events
the incidence of adverse events occurring after a targeted and ultrasound guided prostate biopsy
Pirads score
The Prostate Imaging Reporting and Data System (PIRADS) score classifies MRI lesions on a scale from 1 to 5, which reflects their level of suspicion from least to most. Higher score indicates more suspicion.
Gleason score
The Gleason Score ranges from 1-5 and describes how much the cancer from a biopsy looks like healthy tissue (lower score) or abnormal tissue (higher score). Sum of the gleason grade of the most predominant tumor pattern and a second gleason grade of the second most predominant pattern. Full score from 2 to 10, with higher score indicating more clinically significance.
Full Information
NCT ID
NCT04026763
First Posted
July 17, 2019
Last Updated
July 18, 2019
Sponsor
Icahn School of Medicine at Mount Sinai
Collaborators
Philips Healthcare
1. Study Identification
Unique Protocol Identification Number
NCT04026763
Brief Title
MR/TRUS Fusion Guided Prostate Biopsy
Official Title
MR/TRUS Fusion Guided Prostate Biopsy- An Improved Way To Detect And Quantify Prostate Cancer
Study Type
Interventional
2. Study Status
Record Verification Date
July 2019
Overall Recruitment Status
Unknown status
Study Start Date
May 11, 2018 (Actual)
Primary Completion Date
December 2021 (Anticipated)
Study Completion Date
December 2021 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Icahn School of Medicine at Mount Sinai
Collaborators
Philips Healthcare
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
Yes
Product Manufactured in and Exported from the U.S.
Yes
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
This study will determine if targeted (Magnetic Resonance (MR) / Ultrasound (US) fusion biopsy) plus conventional biopsy is superior to conventional biopsy alone in diagnosing subjects with prostate cancer.
Detailed Description
The efficacy of targeting lesions for surgery may be limited by the visibility of a target during the procedure. The successful outcome of surgical intervention depends upon accurate device placement, which may be very challenging in certain settings, such as when a kidney tumor only is visible for a brief moment during the transient arterial phase of a contrast injection, and soon disappearing on dynamic imaging.
Historically, prostate cancer was diagnosed by digitally guided trans-rectal prostate biopsies. With PSA (Prostate Specific Antigen) screening and improvements in ultrasonography, trans-rectal ultrasound (TRUS) guided prostate biopsy have become the standard of care to screen and diagnose localized prostate cancer. Standard US 12-14 core prostate biopsy is now common practice, detecting cancer in 27% to 44% of patients.
Prostate MR imaging at 3 Tesla magnet dramatically improves diagnostic utility dramatically but biopsies are difficult, time-consuming, and require specialized equipment, which increases the cost significantly.
To meet this challenge TRUS images are overlaid on a previously obtained prostate MRI, combined with an electromagnetic tracking system. The urologist then performs directed prostate biopsies at MR-identified targets in addition to the standard prostate biopsies.
This study will consist of comparison of the standard of care prostate biopsy with the protocol biopsy which consists of a US guided prostate biopsy and a MR/US fusion tracked prostate biopsy. Each patient will act as their own control.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Prostate Disease, Elevated Prostate Specific Antigen, Family History of Prostate Cancer, Positive Digital Rectal Exam
Keywords
Targeted Prostate Biopsy
7. Study Design
Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
520 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Males with Prostate Cancer
Arm Type
Experimental
Arm Description
Each participant will receive standard of care prostate biopsy as well as a US guided prostate biopsy and a MR/TRUS Fusion Guided prostate biopsy guided prostate biopsy.
Intervention Type
Procedure
Intervention Name(s)
prostate biopsy
Intervention Description
standard of care
Intervention Type
Procedure
Intervention Name(s)
MR US Fusion Guided Prostate Biopsy
Other Intervention Name(s)
Fusion Biopsy
Intervention Description
Trans-rectal ultrasound (TRUS) guided fusion prostate biopsy, Transperineal Ultrasound guided fusion prostate biopsy
Intervention Type
Device
Intervention Name(s)
MR/TRUS Fusion Guided Prostate Biopsy
Intervention Description
TRUS images are overlaid on a previously obtained prostate MRI, combined with an electromagnetic tracking system. The urologist then performs directed prostate biopsies at MR-identified targets in addition to the standard prostate biopsies.
Primary Outcome Measure Information:
Title
Incidence of Prostate Cancer
Description
Incidence of diagnosing subjects with prostate cancer with MR visible lesions
Time Frame
Day 0 - day of procedure
Secondary Outcome Measure Information:
Title
Incidence of adverse events
Description
the incidence of adverse events occurring after a targeted and ultrasound guided prostate biopsy
Time Frame
1 month
Title
Pirads score
Description
The Prostate Imaging Reporting and Data System (PIRADS) score classifies MRI lesions on a scale from 1 to 5, which reflects their level of suspicion from least to most. Higher score indicates more suspicion.
Time Frame
1 month
Title
Gleason score
Description
The Gleason Score ranges from 1-5 and describes how much the cancer from a biopsy looks like healthy tissue (lower score) or abnormal tissue (higher score). Sum of the gleason grade of the most predominant tumor pattern and a second gleason grade of the second most predominant pattern. Full score from 2 to 10, with higher score indicating more clinically significance.
Time Frame
1 month
10. Eligibility
Sex
Male
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
All patients must have a pre-operative MRI performed in accordance with the MT Sinai/NIH MR prostate imaging guidelines.
Age greater than 18 years.
No serious concurrent medical illness that would preclude the patient from making a rational informed decision on participation.
The ability to understand and willingness to sign a written informed consent form, and to comply with the protocol. If in question, an ethics consult will be obtained.
Ability to tolerate sedation and or general anesthesia if required.
PSA >2.5 or Abnormal digital rectal exam or current recommendations for biopsy from the American Urological Association
Pre-biopsy prostate MRI as described above, showing targetable lesions within 4 months of biopsy
Able to tolerate a ultrasound guided biopsy
Exclusion Criteria:
Patients with an altered mental status that precludes understanding or consenting for the biopsy procedure will be excluded from this study.
Patients unlikely able to hold reasonably still on a procedure table for the length of the procedure.
Patients with pacemakers or automatic implantable cardiac defibrillators (contraindications to MRI)
Patients with uncorrectable coagulopathies.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Ardeshir Rastinehad, DO
Phone
212-241-4812
Email
art.rastinehad@mountsinai.org
First Name & Middle Initial & Last Name or Official Title & Degree
Cynthia Knauer, RN, MS
Phone
212-241-0751
Email
cynthia.knauer@mountsinai.org
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Ardeshir Rastinehad, DO
Organizational Affiliation
Icahn School of Medicine at Mount Sinai
Official's Role
Principal Investigator
Facility Information:
Facility Name
Icahn School of Medicine at Mount Sinai
City
New York
State/Province
New York
ZIP/Postal Code
11101
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Ardeshir Rastinehad
12. IPD Sharing Statement
Citations:
PubMed Identifier
32956688
Citation
Winoker JS, Wajswol E, Falagario U, Maritini A, Moshier E, Voutsinas N, Knauer CJ, Sfakianos JP, Lewis SC, Taouli BA, Rastinehad AR. Transperineal Versus Transrectal Targeted Biopsy With Use of Electromagnetically-tracked MR/US Fusion Guidance Platform for the Detection of Clinically Significant Prostate Cancer. Urology. 2020 Dec;146:278-286. doi: 10.1016/j.urology.2020.07.072. Epub 2020 Sep 18.
Results Reference
derived
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MR/TRUS Fusion Guided Prostate Biopsy
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