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Diagnostic Value of MRI-targeted Plus Index-lesion-ipsilaterally Systematic Biopsy for Biopsy-naive Men At Risk of Prostate Cancer

Diagnostic Value of MRI-targeted Plus Index-lesion-ipsilaterally Systematic Biopsy for Biopsy-naive Men At Risk of Prostate Cancer: a Prospective, Multicenter, Paired, Non-inferiority Trial

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06584279
Enrollment
563
Registered
2024-09-04
Start date
2024-10-31
Completion date
2025-04-30
Last updated
2024-10-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Prostate Cancer

Brief summary

Targeted and systematic biopsy stands as the prevalent diagnostic approach for prostate cancer. Despite its widespread use, this method is characterized by a high volume of needle biopsies. A refined approach, termed targeted and index-lesion-ipsilateral systematic biopsy, as one of targeted and regional systematic biopsy methods, aim to reduce the number of biopsy cores while maintaining an adequate positive rate. However, the absence of robust evidence necessitates further investigation. This study employs a prospective, multicenter, paired, non-inferiority design to assess the diagnostic efficacy of targeted and index-lesion-ipsilateral systematic prostate biopsy in comparison with the conventional targeted and systematic biopsy for the detection of clinically significant prostate cancer (csPCa). Eligible participants were identified as those with target lesions on prostate MRI, who subsequently underwent targeted and systematic prostate biopsies. The index lesion was defined as the one with the highest Prostate Imaging Reporting and Data System (PI-RADS) score; in cases of multiple lesions with identical PI-RADS scores, the lesion with the greatest diameter was prioritized. Post-biopsy pathological data were collected and evaluated using the International Society of Urological Pathology (ISUP) grading system, which classifies patients with a grade of 2 or higher as having csPCa. The study's primary outcome was to calculate the confidence interval for the difference in csPCa detection rates between the two biopsy methods under a paired design. This interval was then compared against a pre-specified non-inferiority margin to determine whether the targeted and index-lesion-ipsilateral systematic biopsy method is non-inferior to the standard targeted and systematic biopsy in detecting csPCa.

Interventions

DIAGNOSTIC_TESTBiopsy of the prostate and pathological diagnosis

Whether the index-lesion-contralateral systematic biopsy was performed

Sponsors

The Affiliated Nanjing Drum Tower Hospital of Nanjing University Medical School
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
MALE
Age
60 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

* Prostate specific antigen (PSA) \>4 ng/ml; * Prostate Imaging-Reporting and Data System (PI-RADS) score of any lesions on prostate magnetic resonance imaging ≥4 or PI-RADS score of lesions on prostate magnetic resonance imaging = 3 and prostate specific antigen density ≥0.1ng/cm3; * accept prostate biopsy;

Exclusion criteria

* Prostate specific antigen\>20ng/ml; * the location of index lesion on prostate MRI is on the midline of the prostate and symmetrical on both sides; * any contraindication of prostate biopsy; * Previous prostate biopsy; * Previous history of androgen deprivation therapy (ADT), pelvic radiotherapy, and other treatments; * Previous history of transurethral prostatectomy (TURP);

Design outcomes

Primary

MeasureTime frame
Confidence interval for the difference in csPCa detection rate between targeted + index-lesion-ipsilaterally systematic biopsy and targeted + systematic biopsy for biopsy-naive men at risk of prostate cancer0.5-1 years

Secondary

MeasureTime frame
additional value of index-lesion-contralaterally systematic biopsy0.5-1 years
pathological upgrade after radical prostatectomy0.5-1 years

Countries

China

Contacts

Primary ContactHongqian Guo
dr.ghq@nju.edu.cn13605171690
Backup Contactxuefeng Qiu
hydewoods@163.com13776509416

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jun 20, 2026