» Articles » PMID: 28258784

Results of Targeted Biopsy in Men with Magnetic Resonance Imaging Lesions Classified Equivocal, Likely or Highly Likely to Be Clinically Significant Prostate Cancer

Overview
Journal Eur Urol
Specialty Urology
Date 2017 Mar 5
PMID 28258784
Citations 60
Authors
Affiliations
Soon will be listed here.
Abstract

Background: The Prostate Imaging Reporting and Data System (PI-RADS) is the most commonly used scoring system in prostate magnetic resonance imaging (MRI). One of the available techniques to target suspicious lesions is direct in-bore MRI-guided biopsy (MRGB).

Objective: To report on the experience and results of MRGB in a large cohort of patients with lesions classified as equivocal (PI-RADS 3), likely (PI-RADS 4), or highly likely (PI-RADS 5) to be clinically significant (cs) prostate cancer (PCa).

Design, Setting, And Participants: We retrospectively included 1057 patients having MRGB, between January 2012 and September 2016, of lesions classified as PI-RADS≥3 on multiparametric MRI. Biopsy-naïve patients, patients with prior negative systematic transrectal ultrasound-guided biopsy, and patients in active surveillance were included.

Outcome Measurements And Statistical Analysis: The primary outcome measurement is the detection rate of csPCa. Descriptive statistics and chi-square tests were used to calculate the differences in proportions. We considered a Gleason score of ≥3+4 as csPCa.

Results And Limitations: PCa was diagnosed in 35% (55/156), 60% (223/373), and 91% (479/528), and csPCa in 17% (26/156), 34% (128/373), and 67% (352/528) of patients with PI-RADS 3, 4, and 5 lesions, respectively. Follow-up of patients with negative biopsy findings resulted in csPCa in 1.7% (5/300) after a median period of 41 (interquartile range 25-50) mo. The evaluation of prostate-specific antigen density (PSAD) to predict csPCa resulted in 42% of patients with a PI-RADS 3 lesion who could avoid biopsy in case a PSAD of ≥ 0.15ng/ml/ml would be used. In 6% (95% confidence interval, 2-15), csPCa would then be missed. The study is limited because of its retrospective character.

Conclusions: MRGB in lesions scored PI-RADS≥3 yields high detection rates of csPCa in daily clinical practice in cases with previous negative biopsy.

Patient Summary: In daily clinical practice, direct in-bore magnetic resonance imaging-guided biopsy of suspicious lesions reported according to the Prostate Imaging Reporting and Data System yields high detection rates of clinically significant prostate cancer.

Citing Articles

Can lesion volume and prostate-specific antigen density play a role in detecting clinically significant prostate cancer in Prostate Imaging Reporting and Data System-3 lesions on multiparametric magnetic resonance imaging?.

Agrawal S, Prasad V, Menon A, Pooleri G Indian J Urol. 2025; 41(1):35-39.

PMID: 39886626 PMC: 11778701. DOI: 10.4103/iju.iju_112_24.


Using a novel PSMA-PET and PSA-based model to enhance the diagnostic accuracy for clinically significant prostate cancer and avoid unnecessary biopsy in men with PI-RADS ≤ 3 MRI.

Li Y, Li J, Yang J, Xiao L, Zhou M, Cai Y Eur J Nucl Med Mol Imaging. 2024; 52(3):913-924.

PMID: 39404788 DOI: 10.1007/s00259-024-06949-7.


Development and validation of a novel nomogram to avoid unnecessary biopsy in patients with PI-RADS category ≥ 4 lesions and PSA ≤ 20 ng/ml.

Zeng H, Chen Y, Zhao J, Dai J, Xie Y, Wang M World J Urol. 2024; 42(1):495.

PMID: 39177844 DOI: 10.1007/s00345-024-05202-y.


Precision in prostate cancer detection: integrating prostate-specific antigen density (PSAD) and the Prostate Imaging Reporting and Data System (PI-RADS) to provide additional risk stratification for a more accurate diagnostic decision.

Hruba T, Kubas V, Franko M, Balaz V, Spurny M, Mistinova J Ir J Med Sci. 2024; 193(6):2635-2642.

PMID: 39093531 PMC: 11666638. DOI: 10.1007/s11845-024-03771-w.


A comparative study of F-PSMA-1007 PET/CT and pelvic MRI in newly diagnosed prostate cancer.

Ye Z, Kou Y, Shen J, Dang J, Tan X, Jiang X BMC Med Imaging. 2024; 24(1):192.

PMID: 39080625 PMC: 11290235. DOI: 10.1186/s12880-024-01376-4.