Abstract

ObjectivesTo create a radiomics approach based on multiparametric magnetic resonance imaging (mpMRI) features extracted from an auto-fixed volume of interest (VOI) that quantifies the phenotype of clinically significant (CS) peripheral zone (PZ) prostate cancer (PCa).MethodsThis study included 206 patients with 262 prospectively called mpMRI prostate imaging reporting and data system 3–5 PZ lesions. Gleason scores > 6 were defined as CS PCa. Features were extracted with an auto-fixed 12-mm spherical VOI placed around a pin point in each lesion. The value of dynamic contrast-enhanced imaging(DCE), multivariate feature selection and extreme gradient boosting (XGB) vs. univariate feature selection and random forest (RF), expert-based feature pre-selection, and the addition of image filters was investigated using the training (171 lesions) and test (91 lesions) datasets.ResultsThe best model with features from T2-weighted (T2-w) + diffusion-weighted imaging (DWI) + DCE had an area under the curve (AUC) of 0.870 (95% CI 0.980–0.754). Removal of DCE features decreased AUC to 0.816 (95% CI 0.920–0.710), although not significantly (p = 0.119). Multivariate and XGB outperformed univariate and RF (p = 0.028). Expert-based feature pre-selection and image filters had no significant contribution.ConclusionsThe phenotype of CS PZ PCa lesions can be quantified using a radiomics approach based on features extracted from T2-w + DWI using an auto-fixed VOI. Although DCE features improve diagnostic performance, this is not statistically significant. Multivariate feature selection and XGB should be preferred over univariate feature selection and RF. The developed model may be a valuable addition to traditional visual assessment in diagnosing CS PZ PCa.Key Points• T2-weighted and diffusion-weighted imaging features are essential components of a radiomics model for clinically significant prostate cancer; addition of dynamic contrast-enhanced imaging does not significantly improve diagnostic performance.• Multivariate feature selection and extreme gradient outperform univariate feature selection and random forest.• The developed radiomics model that extracts multiparametric MRI features with an auto-fixed volume of interest may be a valuable addition to visual assessment in diagnosing clinically significant prostate cancer.

Highlights

  • Prostate cancer (PCa) is currently the most common cancer among men, and comprises approximately 20% of all cancers in the western world [1, 2]

  • The developed radiomics model that extracts multiparametric MRI features with an auto-fixed volume of interest may be a valuable addition to visual assessment in diagnosing clinically significant prostate cancer

  • The comparison of models based on the two different multiparametric magnetic resonance imaging (mpMRI) datasets (T2-w + diffusion-weighted imaging (DWI) vs. T2-w + DWI + DCE) showed that the addition of DCE imaging did lead to a significant improvement on the training dataset (p < 0.001, Table 3)

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Summary

Introduction

Prostate cancer (PCa) is currently the most common cancer among men, and comprises approximately 20% of all cancers in the western world [1, 2]. Most patients with PCa can be successfully treated [3], it is still responsible for an estimated 10% of all male cancerrelated deaths in the western world. Prostate-specific antigen (PSA) testing with digital rectal examination (DRE) followed by transrectal ultrasound (TRUS) biopsy is a widely used diagnostic algorithm. PSA testing suffers from a high number of false positives combined with a considerable number of false negatives [4]. The high falsepositive rate leads to unnecessary TRUS biopsies. The diagnostic limitations of PSA testing followed by TRUS biopsies lead to unnecessary patient discomfort, anxiety, and complications [6]

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