Micro-ultrasound compared with MRI-targeted biopsy in detecting clinically significant prostate cancer: Systematic review and meta-analysis.
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
Journal Info
Journal of Clinical Oncology
Lippincott Williams & Wilkins
Authors (13)
Caio Suartz
Northern Ontario School of Medicine, Thunder Bay, ON, Canada
José Pedro Cassemiro Micheleto
University of São Paulo, São Paulo, Brazil
Tallys Ávila Suzuki
University of São Paulo, São Paulo, Brazil
Lucas Amorim Santos
University of São Paulo, São Paulo, Brazil
Roberto Iglesias Lopes
University of São Paulo, São Paulo, Brazil
Bárbara Miranda Martins
University of São Paulo, São Paulo, Brazil
Bárbara Melão
Adventist Health, Manaus, Brazil
Mauricio Cordeiro
Urology Department, Instituto do Câncer do Estado de São Paulo, São Paulo, Brazil
Walid Sharour
Northern Ontario School of Medicine, Thunder Bay, ON, Canada
Walid Shabana
Northern Ontario School of Medicine, Thunder Bay, ON, Canada
Leopoldo Alves Ribeiro-Filho
Instituto do Câncer do Estado de São Paulo (ICESP), Universidade de São Paulo, São Paulo, Brazil
Leonardo Oliveira Reis
Unicamp, Campinas, Brazil
William Carlos Nahas
Instituto do Câncer do Estado de São Paulo, São Paulo, Brazil