Micro-ultrasound compared with MRI-targeted biopsy in detecting clinically significant prostate cancer: Systematic review and meta-analysis.

C Caio Suartz (Northern Ontario School of Medicine, Thunder Bay, ON, Canada) J José Pedro Cassemiro Micheleto (University of São Paulo, São Paulo, Brazil) T Tallys Ávila Suzuki (University of São Paulo, São Paulo, Brazil) L Lucas Amorim Santos (University of São Paulo, São Paulo, Brazil) R Roberto Iglesias Lopes (University of São Paulo, São Paulo, Brazil) B Bárbara Miranda Martins (University of São Paulo, São Paulo, Brazil) B Bárbara Melão (Adventist Health, Manaus, Brazil) M Mauricio Cordeiro (Urology Department, Instituto do Câncer do Estado de São Paulo, São Paulo, Brazil) W Walid Sharour (Northern Ontario School of Medicine, Thunder Bay, ON, Canada) W Walid Shabana (Northern Ontario School of Medicine, Thunder Bay, ON, Canada) L Leopoldo Alves Ribeiro-Filho (Instituto do Câncer do Estado de São Paulo (ICESP), Universidade de São Paulo, São Paulo, Brazil) L Leonardo Oliveira Reis (Unicamp, Campinas, Brazil) W William Carlos Nahas (Instituto do Câncer do Estado de São Paulo, São Paulo, Brazil)

Abstract

318 Background: Prostate cancer is highly prevalent, and diagnostic pathways must maximize detection of clinically significant disease (csPCa) while minimizing overdiagnosis and resource burden. Micro-ultrasound (microUS) offers real-time, high-resolution lesion targeting and could reduce reliance on pre-biopsy MRI. We compared csPCa detection and diagnostic accuracy between microUS-targeted biopsy (microUS-TBx) and MRI-targeted biopsy (MRI-TBx). Methods: Systematic searches of MEDLINE (PubMed), Embase, and ClinicalTrials.gov were completed on July 4, 2025 and updated Aug 5, 2025. Eligible studies directly compared microUS-TBx with MRI-TBx in adults undergoing prostate biopsy and reported csPCa (typically ISUP ≥2). Primary endpoint: per-patient csPCa detection. Secondary endpoints: sensitivity and specificity for csPCa. Random-effects meta-analysis (Hartung-Knapp) estimated detection ratios (microUS/MRI); heterogeneity was summarized with I². Diagnostic accuracy was synthesized using a bivariate random-effects model. Prespecified analyses included biopsy-naïve status, use of concomitant systematic cores, and risk of bias (QUADAS-2). PROSPERO registration pending at submission. Results: Twenty-two studies (including one randomized trial) were included. Micro-US-TBx detected 2,194 csPCa cases; MRI-TBx detected 2,237. The pooled detection ratio (Micro-US vs MRI) was 0.99 (95% CI, 0.88–1.11; I² = 78.5%), indicating comparable yield. Pooled sensitivity/specificity were 0.86/0.38 for Micro-US-TBx and 0.84/0.40 for MRI-TBx. Heterogeneous biopsy triggers (e.g., PI-RADS ≥3 only vs biopsy-all) and frequent use of concomitant systematic biopsy introduced spectrum and partial verification/incorporation biases, which may shift detection rates, limit generalizability to routine care, and obscure standalone modality accuracy. Conclusions: Micro-US-TBx demonstrated csPCa detection and diagnostic accuracy comparable to MRI-TBx. Given potential advantages in access and cost, MicroUS is a viable alternative for integration into prostate cancer diagnostic pathways, particularly in resource-limited settings.

Article Details

Volume / Issue Vol. 44, Issue 7_suppl
Published March 01, 2026
Pages 318-318
ISSN 0732-183X
Publisher Lippincott Williams & Wilkins

Journal Info

Journal of Clinical Oncology

Lippincott Williams & Wilkins

ISSN: 0732-183X Health Sciences

Authors (13)

C

Caio Suartz

Northern Ontario School of Medicine, Thunder Bay, ON, Canada

J

José Pedro Cassemiro Micheleto

University of São Paulo, São Paulo, Brazil

T

Tallys Ávila Suzuki

University of São Paulo, São Paulo, Brazil

L

Lucas Amorim Santos

University of São Paulo, São Paulo, Brazil

R

Roberto Iglesias Lopes

University of São Paulo, São Paulo, Brazil

B

Bárbara Miranda Martins

University of São Paulo, São Paulo, Brazil

B

Bárbara Melão

Adventist Health, Manaus, Brazil

M

Mauricio Cordeiro

Urology Department, Instituto do Câncer do Estado de São Paulo, São Paulo, Brazil

W

Walid Sharour

Northern Ontario School of Medicine, Thunder Bay, ON, Canada

W

Walid Shabana

Northern Ontario School of Medicine, Thunder Bay, ON, Canada

L

Leopoldo Alves Ribeiro-Filho

Instituto do Câncer do Estado de São Paulo (ICESP), Universidade de São Paulo, São Paulo, Brazil

L

Leonardo Oliveira Reis

Unicamp, Campinas, Brazil

W

William Carlos Nahas

Instituto do Câncer do Estado de São Paulo, São Paulo, Brazil