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February 8, 2026Cancer Medicine0 citationsOpen Access

Preoperative Multiparametric MRI ‐Based Tumour–Periprostatic Adipose Tissue Interface Characterisation for Extraprostatic Extension Prediction in Prostate Cancer

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SZS ZhangLHLeiming HuoZZZhitao Zhu

Key Points

  • To assess the predictive value of tumour–periprostatic adipose tissue interface features on mpMRI for extraprostatic extension in prostate cancer.
  • Conducted a single-centre retrospective cohort study with 240 patients who underwent radical prostatectomy.
  • Measured five interface features on mpMRI: contact length, contact angle, T2 signal intensity ratio, diffusion coefficient, and capsular integrity score.
  • Developed a combined predictive model integrating interface features with a baseline clinical model, including PSA metrics.
  • Performed bootstrap internal validation with 1000 iterations to assess model performance using AUC and decision curve analysis.
  • Extraprostatic extension was observed in 34.2% of patients (82 out of 240).
  • The combined predictive model achieved a bias-corrected AUC of 0.823, outperforming the baseline model's AUC of 0.744.
  • Decision curve analysis indicated a higher net benefit for the combined model across threshold probabilities, showing clinical relevance.

Abstract

ABSTRACT Objective To evaluate the independent predictive value of tumour–periprostatic adipose tissue (PPAT) interface features on preoperative multiparametric magnetic resonance imaging (mpMRI) for extraprostatic extension (EPE) in prostate cancer and to compare discrimination and clinical net benefit with a baseline clinical model. Methods This single‐centre retrospective cohort included patients who underwent radical prostatectomy with mpMRI completed within 8 weeks. On a single axial slice at maximum tumour diameter, five simplified interface features were measured using standard PACS tools: contact length, contact angle, T2 signal intensity ratio, interface apparent diffusion coefficient (3‐mm annular zone) and capsular integrity score (0–2 scale). A baseline clinical model (prostate‐specific antigen PSA, PSA density, PI‐RADS and biopsy Gleason score) and a combined model (baseline variables plus LASSO‐selected interface features) were constructed. Bootstrap internal validation (1000 iterations) with bias correction was performed. Discrimination was assessed using the area under the curve (AUC), and calibration curves and decision curve analysis evaluated accuracy and net clinical benefit. Results A total of 240 patients were included, with an EPE prevalence of 34.2% (82/240). The combined model achieved a bias‐corrected AUC of 0.823 (95% confidence interval CI: 0.768–0.878), suggesting improvement over the baseline model's AUC of 0.744 (95% CI: 0.680–0.808). Decision curve analysis revealed a higher net benefit for the combined model across clinically relevant threshold probabilities (10%–50%). Conclusions Simplified tumour–PPAT interface features independently predict EPE without increasing imaging complexity, improving discrimination and clinical value for preoperative risk stratification.

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Cite This Study

Zhang et al. (2026) studied this question.

synapsesocial.com/papers/698828100fc35cd7a88472c2https://doi.org/10.1002/cam4.71613
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Also Consider

Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:

  1. 1Periprostatic Fat Thickness on MRI: Correlation With Gleason Score in Prostate Cancer2014 · 73 citations
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  3. 3Periprostatic Adipose Tissue Microenvironment: Metabolic and Hormonal Pathways During Prostate Cancer Progression2022 · 22 citations
  4. 4Length of capsular contact on prostate MRI as a predictor of extracapsular extension: which is the most optimal sequence?2016 · 35 citations
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