# Artificial intelligence-derived transition zone PSA density as a triage tool to reduce unnecessary prostate systematic biopsies in MRI-negative men

**Authors:** Jiaheng Shang, Jingyun Wu, Ruiyi Deng, Meixia Shang, Pengsheng Wu, Jianhui Qiu, Jingcheng Zhou, Lin Cai, Xiaoying Wang, Kan Gong, Yi Liu

PMC · DOI: 10.1186/s13244-026-02221-8 · 2026-02-10

## TL;DR

This study shows that a new AI-based measure of prostate-specific antigen density can better predict significant prostate cancer in men with negative MRI scans, potentially reducing unnecessary biopsies.

## Contribution

The study introduces AI-derived transition zone PSA density as a superior triage tool for detecting clinically significant prostate cancer in MRI-negative patients.

## Key findings

- TZ-PSAD outperformed conventional PSAD with an AUC of 0.718 versus 0.686.
- A TZ-PSAD threshold of 0.35 ng/mL/cc identified 20.1% csPCa cases versus 4.1% below threshold.
- TZ-PSAD was a strong independent predictor of imaging-invisible csPCa.

## Abstract

The study aimed to assess the predictive performance of transition zone PSA density (TZ-PSAD) compared to conventional PSA density (PSAD) in detecting clinically significant prostate cancer (csPCa) among patients with negative pre-biopsy MRI findings.

The study included 606 patients with negative MRI findings who subsequently underwent transrectal ultrasound-guided systematic biopsy. AI software automatically measured prostate and zonal volumes, from which PSAD and TZ-PSAD (total PSA/transition zone volume) were calculated. Diagnostic performances were evaluated using ROC curve analysis, risk stratification was applied to select patients needing biopsy, and independent predictors of imaging-invisible csPCa were determined through univariate and multivariate analyses.

51 patients (8.4%) were diagnosed with csPCa. TZ-PSAD demonstrated significant superior discriminative ability (AUC = 0.718) compared to PSAD (AUC = 0.686; p = 0.019). Patients with TZ-PSAD ≥ 0.35 ng/mL/cc had a csPCa detection rate of 20.1%, while those below this threshold had a rate of 4.1%. The optimal TZ-PSAD threshold of 0.35 ng/mL/cc showed superior performance than the guideline-recommended PSAD threshold of 0.2 ng/mL/cc. Multivariate analysis identified TZ-PSAD as a strong independent predictor of imaging-invisible csPCa.

TZ-PSAD outperforms conventional PSAD in predicting csPCa among men with negative MRI, offering a valuable tool for risk stratification. This facilitates individualized risk assessment, potentially reducing unnecessary biopsies and optimizing patient management.

Our AI system delivers accurate and reproducible prostate zone segmentation, while TZ-PSAD derived from AI outperforms conventional PSAD in detecting csPCa in MRI-negative patients and serves as an effective triage tool to optimize biopsy decision-making and reduce unnecessary systematic biopsies.

Our AI system enables accurate and reproducible segmentation and measurement of prostate zones.TZ-PSAD demonstrates significantly superior diagnostic performance over conventional PSAD for identifying men with a negative MRI who will have csPCa on a systematic biopsy.TZ-PSAD represents an effective triage metric to reduce unwarranted systematic biopsies in MRI-negative patients.

Our AI system enables accurate and reproducible segmentation and measurement of prostate zones.

TZ-PSAD demonstrates significantly superior diagnostic performance over conventional PSAD for identifying men with a negative MRI who will have csPCa on a systematic biopsy.

TZ-PSAD represents an effective triage metric to reduce unwarranted systematic biopsies in MRI-negative patients.

## Linked entities

- **Diseases:** prostate cancer (MONDO:0005159)

## Full-text entities

- **Genes:** NPEPPS (aminopeptidase puromycin sensitive) [NCBI Gene 9520] {aka AAP-S, MP100, PSA}
- **Diseases:** csPCa (MESH:D011471)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12891307/full.md

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Source: https://tomesphere.com/paper/PMC12891307