The Primacy of High B-Value 3T-DWI Radiomics in the Prediction of Clinically Significant Prostate Cancer

Predicting clinically significant prostate cancer (csPCa) is crucial in PCa management. 3T-magnetic resonance (MR) systems may have a novel role in quantitative imaging and early csPCa prediction, accordingly. In this study, we develop a radiomic model for predicting csPCa based solely on native b20...

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Veröffentlicht in:Diagnostics (Basel) 2021-04, Vol.11 (5), p.739
Hauptverfasser: Bevilacqua, Alessandro, Mottola, Margherita, Ferroni, Fabio, Rossi, Alice, Gavelli, Giampaolo, Barone, Domenico
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Sprache:eng
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Zusammenfassung:Predicting clinically significant prostate cancer (csPCa) is crucial in PCa management. 3T-magnetic resonance (MR) systems may have a novel role in quantitative imaging and early csPCa prediction, accordingly. In this study, we develop a radiomic model for predicting csPCa based solely on native b2000 diffusion weighted imaging (DWI ) and debate the effectiveness of apparent diffusion coefficient (ADC) in the same task. In total, 105 patients were retrospectively enrolled between January-November 2020, with confirmed csPCa or ncsPCa based on biopsy. DWI and ADC images acquired with a 3T-MRI were analyzed by computing 84 local first-order radiomic features (RFs). Two predictive models were built based on DWI and ADC, separately. Relevant RFs were selected through LASSO, a support vector machine (SVM) classifier was trained using repeated 3-fold cross validation (CV) and validated on a holdout set. The SVM models rely on a single couple of uncorrelated RFs (ρ < 0.15) selected through Wilcoxon rank-sum test ( ≤ 0.05) with Holm-Bonferroni correction. On the holdout set, while the ADC model yielded AUC = 0.76 (95% CI, 0.63-0.96), the DWI model reached AUC = 0.84 (95% CI, 0.63-0.90), with specificity = 75%, sensitivity = 90%, and informedness = 0.65. This study establishes the primary role of 3T-DWI in PCa quantitative analyses, whilst ADC can remain the leading sequence for detection.
ISSN:2075-4418
2075-4418
DOI:10.3390/diagnostics11050739