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Ultrasound echogenicity is complementary to PI-RADS for risk stratification of clinically significant prostate cancer

Abstract

Background

The combination of multiparametric magnetic resonance imaging (MP-MRI) and ultrasound-guided fusion biopsy is increasingly recognized as a valuable tool for diagnosing prostate cancer. However, up to 80% of PI-RADS 3 lesions and 50% of PI-RADS 4 lesions are benign. This study evaluates whether lesion echogenicity observed during MRI-ultrasound fusion biopsy is associated with detecting clinically significant prostate cancer (csPCa).

Methods

In this retrospective analysis (March 2017–February 2022), we reviewed patients who underwent both standard 12-core random biopsies and targeted MP-MRI/US fusion-guided biopsies at our institution. Lesions were categorized as strongly hypoechoic, weakly hypoechoic, or non-hypoechoic based on ultrasound echogenicity. CsPCa was defined as a Gleason score ≥7.

Results

Among 222 biopsy patients, 59.3% were diagnosed with PCa, and 68% had csPCa. Of 420 lesions, 19.1% were strongly hypoechoic (45% csPCa), 29.5% were weakly hypoechoic (25% csPCa), and 51.4% were non-hypoechoic (11.8% csPCa) (p < 0.001). Echogenicity improved csPCa detection for PI-RADS ≤ 3 lesions from 7.5% (non-hypoechoic) to 27.5% (strongly hypoechoic), for PI-RADS 4 from 13.1% to 35.1%, and for PI-RADS 5 from 42% to 63.5%. The ROC analysis demonstrated AUCs of 0.6958 for PI-RADS, 0.6929 for echogenicity, and 0.7434 for their combination (all p < 0.001).

Conclusion

Lesion echogenicity observed during MRI-ultrasound fusion biopsy enhances csPCa detection and complements PI-RADS scoring. Incorporating echogenicity into risk assessment may improve biopsy decision-making and diagnostic accuracy.

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Fig. 1: Proportional distribution of Gleason scores across echogenicity categories.
Fig. 2
Fig. 3
Fig. 4: Proportional distribution of Gleason scores by echogenicity, stratified by PI-RADS score and PSAD.

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Data availability

The data supporting the findings of this study are available from the corresponding author upon reasonable request.

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Acknowledgements

An abstract of this study was published as part of three conferences: American Urological Association 2024, Mid-Atlantic American Urological Association 2024, and Society of Urologic Oncology 2023. 1. Society of Urologic Oncology: (https://doi.org/10.1016/j.urolonc.2024.01.215). Urologic Oncology: Seminars and Original Investigations. 24th Annual Meeting of the Society of Urologic Oncology, November 28th to December 1st, 2023, Washington DC, USA. https://suo-abstracts.secure-platform.com/a/gallery?roundId=18. 2. Mid-Atlantic American Urologic Association:https://www.canjurol.com/html/free-articles/2024/31-04S1/CJU_V31I3_04S1_03_Abstracts_Aug_Supplement_2024_MAAUAS.pdf. The Canadian Journal of Urology. 82nd Annual Meeting of the Mid-Atlantic Section of the American Urological Association, September 5th to 7th, 2024, White Sulphur Springs, West Virginia, USA. https://auau.auanet.org/content/MAAUA2024. 3. American Urologic Association: (https://doi.org/10.1097/01.JU.0001008672.83391.ed.05) The 2024 Annual Meeting of the American Urological Association, May 3rd to 6th, San Antonio, Texas, USA. https://www.auajournals.org/toc/juro/211/5S.

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Authors and Affiliations

Authors

Contributions

GW: data collection, data analysis, figure preparation, drafting of the original manuscript. AK: data analysis, statistical support, figure editing, writing, and revision of the manuscript. MP: data collection, hypothesis generation, assistance with manuscript drafting. SW: initial conceptualization, data collection, and critical input on study design. AJVB: hypothesis generation, initial conceptualization, critical input on study design. MN: provision of resources, critical review of the manuscript. MMS: overall supervision, provision of resources, hypothesis generation, manuscript editing and review, project administration, and guidance.

Corresponding author

Correspondence to Mohummad Minhaj Siddiqui.

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The authors declare no competing interests.

Ethics approval and consent to participate

All methods were performed in accordance with the relevant guidelines and regulations. Ethical approval for this study was obtained from the University of Maryland, Baltimore Institutional Review Board (IRB) [Protocol/Reference Number: HP-00065772]. Informed consent was not required because of the retrospective nature of the study.

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Wegner, G., Khan, A., Panagos, M. et al. Ultrasound echogenicity is complementary to PI-RADS for risk stratification of clinically significant prostate cancer. Prostate Cancer Prostatic Dis (2025). https://doi.org/10.1038/s41391-025-01033-z

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