Multiparametric MRI and auto-fixed volume of interest-based radiomics signature for clinically significant peripheral

Jeroen Bleker1, Thomas C Kwee2, Rudi A J O Dierckx2

  • 1Medical Imaging Center, Departments of Radiology, Nuclear Medicine and Molecular Imaging, University Medical Center Groningen, University of Groningen, Hanzeplein 1, 9700 RB, Groningen, The Netherlands. j.bleker@umcg.nl.

European Radiology
|November 29, 2019
PubMed
Abstract

Insights

This study developed a radiomics approach using multiparametric MRI to quantify clinically significant prostate cancer. T2-weighted and diffusion-weighted imaging features are key, with dynamic contrast-enhanced imaging offering no significant diagnostic improvement.

Area of Science:

  • Radiology
  • Oncology
  • Medical Imaging Analysis

Background:

  • Prostate cancer diagnosis relies on accurate tumor characterization.
  • Multiparametric magnetic resonance imaging (mpMRI) offers detailed insights into prostate tissue.
  • Quantifying the phenotype of clinically significant (CS) peripheral zone (PZ) prostate cancer (PCa) remains a challenge.

Purpose of the Study:

  • To develop a radiomics approach using mpMRI features from an auto-fixed volume of interest (VOI).
  • To quantify the phenotype of CS PZ PCa.
  • To evaluate the contribution of different imaging sequences and feature selection methods.

Main Methods:

  • mpMRI data from 206 patients with 262 PZ lesions (PI-RADS 3-5) were analyzed.
  • Features were extracted from a 12-mm spherical VOI placed in each lesion.
  • The study compared dynamic contrast-enhanced (DCE) imaging, multivariate (XGBoost) vs. univariate (Random Forest) feature selection, and image filters.

Main Results:

  • The best model combining T2-weighted (T2-w) + diffusion-weighted imaging (DWI) + DCE achieved an AUC of 0.870.
  • Excluding DCE features reduced AUC to 0.816 (p=0.119), indicating no significant impact.
  • Multivariate feature selection with XGBoost outperformed univariate selection with Random Forest (p=0.028).

Conclusions:

  • A radiomics approach using T2-w + DWI features from an auto-fixed VOI can quantify CS PZ PCa phenotype.
  • DCE imaging does not significantly improve diagnostic performance.
  • Multivariate feature selection and XGBoost are preferred methods for developing such radiomics models.