Prospective Multicenter, Randomized Study Comparing the Diagnostic Efficacy of a Targeted MRI/Ultrasound Fusion-guided Prostate Biopsy Versus a Systematic Transrectal Ultrasound-guided Biopsy in Men With at Least on Negative Prostate Biopsy
Overview
- Phase
- N/A
- Intervention
- Not specified
- Conditions
- Prostate Cancer
- Sponsor
- Heinrich-Heine University, Duesseldorf
- Enrollment
- 586
- Locations
- 3
- Primary Endpoint
- Detection rate of significant prostate cancers
- Last Updated
- 10 years ago
Overview
Brief Summary
Patients will be submitted to a multiparametric MRI examination of the prostate. Subsequently, all participants will be randomized (1:1) into both study arms. In study arm A patients will be submitted to the gold-standard which comprises systematic transrectal ultrasound-guided prostate biopsy. In study arm B patients will be submitted to targeted prostate biopsy based on the multiparametric MRI findings.
Detailed Description
In men with previously negative prostate biopsy and persistent elevated prostate-specific antigen (PSA) value, it is unclear which biopsy strategy offers the highest detection rate for significant prostate cancer. The hypothesis of this study is that targeted MRI/ultrasound fusion-guided biopsy improves the detection rates of significant prostate cancers compared with systematic transrectal ultrasound-guided prostate biopsy. Men with at least one previously negative transrectal ultrasound-guided biopsy and persistently elevated PSA values (\> 3 ng/ml) or PSA velocity \>0.75 ng/ml/p.a. will be submitted to a multiparametric MRI examination of the prostate. Subsequently, all participants will be randomized (1:1) into both study arms. In study arm A patients will be submitted to the gold-standard which comprises systematic transrectal ultrasound--guided prostate biopsy. In study arm B patients will be submitted to targeted prostate biopsy based on the multiparametric MRI findings. Targeted biopsies will be performed using MRI/ultrasound fusion-guided.
Investigators
Eligibility Criteria
Inclusion Criteria
- •At least one negative transrectal ultrasound-guided prostate biopsy
- •PSA \> 3.0 ng/ml or PSA velocity \>0.75 ng/ml/p.a.
Exclusion Criteria
- •Known prostate cancer
- •PSA \>50 ng/ml
- •Previous MRI-targeted prostate biopsy
Outcomes
Primary Outcomes
Detection rate of significant prostate cancers
Time Frame: One week after biopsy
Secondary Outcomes
- Overall detection rate of prostate cancers(One week after biopsy)