Targeted Biopsy or Standard Biopsy for Clinical Significant Prostate Cancer Detection
Primary Purpose
Prostate Neoplasm
Status
Unknown status
Phase
Not Applicable
Locations
China
Study Type
Interventional
Intervention
Targeted prostate biopsy
Standard biopsy
Sponsored by
About this trial
This is an interventional diagnostic trial for Prostate Neoplasm
Eligibility Criteria
Inclusion Criteria:
- Men more than 18 years old with clinical suspicion of prostate cancer;
- Serum PSA ≤ 20 ng/ml within the previous 3 months;
- Suspected stage ≤ T2 on rectal examination (organ-confined prostate cancer) within the previous 3 months;
- No evidence of PSA increase by noncancerous factors, such as catheterization, bladder stones, or urinary tract infection including bacterial prostatitis;
- mpMRI PI-RADS V2 score 4 or 5;
- Able to provide written informed consent.
Exclusion Criteria:
- Prior prostate biopsy or prostate surgery;
- Prior treatment for prostate cancer;
- Contraindication to MRI (e.g. claustrophobia, pacemaker, estimated glomerular filtration rate ≤ 50mls/min);
- Contraindication to prostate biopsy.
Sites / Locations
- Department of Urology, Drum Tower Hospital, Medical School of Nanjing University, Institute of Urology, Nanjing UniversityRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
target biopsy group
standard biopsy group
Arm Description
Targeted prostate biopsy
Standard prostate biopsy
Outcomes
Primary Outcome Measures
Detection rates of clinically significant PCa
Clinically significant prostate cancer is considered as: biopsy Gleason score ≥3+4 or maximum cancer core length ≥5 mm.
Secondary Outcome Measures
Detection rates of clinically insignificant PCa
Clinically insignificant prostate cancer is considered as: biopsy Gleason score <3+4 and maximum cancer core length <5 mm.
Biopsy-related adverse events
Proportion of men undergoing radical prostatectomy who have Gleason grade upgrading
Comparing the Gleason grades (from 1-5, the bigger the worse) between biopsy and final pathology, Gleason grade is upgrading when the Gleason grade of final pathology is bigger than that of biopsy.
Full Information
NCT ID
NCT03572946
First Posted
June 19, 2018
Last Updated
October 10, 2019
Sponsor
The Affiliated Nanjing Drum Tower Hospital of Nanjing University Medical School
1. Study Identification
Unique Protocol Identification Number
NCT03572946
Brief Title
Targeted Biopsy or Standard Biopsy for Clinical Significant Prostate Cancer Detection
Official Title
Diagnostic Efficiency With Magnetic Resonance Imaging-targeted Biopsy Compared to Standard Transperineal Ultrasound-guided Biopsy in Biopsy-naïve Suspicious Prostate Cancer Patients: A Randomized Controlled Trial
Study Type
Interventional
2. Study Status
Record Verification Date
October 2018
Overall Recruitment Status
Unknown status
Study Start Date
October 9, 2018 (Actual)
Primary Completion Date
October 2019 (Anticipated)
Study Completion Date
December 2019 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
The Affiliated Nanjing Drum Tower Hospital of Nanjing University Medical School
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
This randomized controlled trial aims to assess the detection rate of clinically significant and clinically insignificant cancer of mpMRI-targeted biopsy compared to transperineal standard biopsy in men with clinical suspicion of prostate cancer who had no prior prostate biopsy.
Detailed Description
Prostate biopsy with multiple samples using a standardized template (standard biopsy, SB) under transrectal ultrasound (TRUS) guidance is the current standard diagnostic approach in suspicion of prostate cancer (PCa). However, many biopsies are unnecessary or cannot detect clinically significant PCa (csPCa).
With the introduction of multiparametric magnetic resonance imaging (mpMRI) of the prostate and the improvement for PCa detection and localization, an alternative procedure, known as MRI-targeted biopsy (TB), has been shown comparable or even higher detection rates of csPCa compared to TRUS-biopsy (SB).
This randomized controlled trial aims to assess the detection rate of clinically significant and clinically insignificant cancer of TB compared to SB (transperineal) in men referred with clinical suspicion of prostate cancer who have had no prior prostate biopsy.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Prostate Neoplasm
7. Study Design
Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
400 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
target biopsy group
Arm Type
Experimental
Arm Description
Targeted prostate biopsy
Arm Title
standard biopsy group
Arm Type
Active Comparator
Arm Description
Standard prostate biopsy
Intervention Type
Procedure
Intervention Name(s)
Targeted prostate biopsy
Intervention Description
MRI-guided targeted prostate biopsy
Intervention Type
Procedure
Intervention Name(s)
Standard biopsy
Intervention Description
Transperineal ultrasound guided prostate biopsy(SB).
Primary Outcome Measure Information:
Title
Detection rates of clinically significant PCa
Description
Clinically significant prostate cancer is considered as: biopsy Gleason score ≥3+4 or maximum cancer core length ≥5 mm.
Time Frame
30 days post biopsy
Secondary Outcome Measure Information:
Title
Detection rates of clinically insignificant PCa
Description
Clinically insignificant prostate cancer is considered as: biopsy Gleason score <3+4 and maximum cancer core length <5 mm.
Time Frame
30 days post biopsy
Title
Biopsy-related adverse events
Time Frame
30 days post biopsy
Title
Proportion of men undergoing radical prostatectomy who have Gleason grade upgrading
Description
Comparing the Gleason grades (from 1-5, the bigger the worse) between biopsy and final pathology, Gleason grade is upgrading when the Gleason grade of final pathology is bigger than that of biopsy.
Time Frame
90 days post-biopsy
10. Eligibility
Sex
Male
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Men more than 18 years old with clinical suspicion of prostate cancer;
Serum PSA ≤ 20 ng/ml within the previous 3 months;
Suspected stage ≤ T2 on rectal examination (organ-confined prostate cancer) within the previous 3 months;
No evidence of PSA increase by noncancerous factors, such as catheterization, bladder stones, or urinary tract infection including bacterial prostatitis;
mpMRI PI-RADS V2 score 4 or 5;
Able to provide written informed consent.
Exclusion Criteria:
Prior prostate biopsy or prostate surgery;
Prior treatment for prostate cancer;
Contraindication to MRI (e.g. claustrophobia, pacemaker, estimated glomerular filtration rate ≤ 50mls/min);
Contraindication to prostate biopsy.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Hongqian Guo, PhD
Phone
8613605171690
Email
dr.ghq@nju.edu.cn
First Name & Middle Initial & Last Name or Official Title & Degree
Jie Gao, Bachelor
Phone
8613951784909
Email
medgaojie@163.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Hongqian Guo, PhD
Organizational Affiliation
The Affiliated Nanjing Drum Tower Hospital of Nanjing University Medical School
Official's Role
Study Chair
Facility Information:
Facility Name
Department of Urology, Drum Tower Hospital, Medical School of Nanjing University, Institute of Urology, Nanjing University
City
Nanjing
State/Province
Jiangsu
ZIP/Postal Code
210000
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Jie Gao, MD
Phone
8613951784909
Email
medgaojie@163.com
12. IPD Sharing Statement
Learn more about this trial
Targeted Biopsy or Standard Biopsy for Clinical Significant Prostate Cancer Detection
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