Novel Radiomic Analysis on Bi-parametric MRI for Characterizing Differences Between MR Non-visible and Visible Clinically Significant Prostate Cancer
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Background: around one third of clinically significant prostate cancer (CsPCa) foci are reported to be MRI non-visible (MRI─).
Objective: To quantify the differences between MR visible (MRI+) and MRI CsPCa using intra- and peri-lesional radiomic features on bi-parametric MRI (bpMRI).
Methods: This retrospective and multi-institutional study comprised 164 patients with pre-biopsy 3T prostate multi-parametric MRI from 2014 to 2017. The MRI CsPCa referred to lesions with PI-RADS v2 score < 3 but ISUP grade group > 1. Three experienced radiologists were involved in annotating lesions and PI-RADS assignment. The validation set (D) comprised 52 patients from a single institution, the remaining 112 patients were used for training (D). 200 radiomic features were extracted from intra-lesional and peri-lesional regions on bpMRI.Logistic regression with least absolute shrinkage and selection operator (LASSO) and 10-fold cross-validation was applied on D to identify radiomic features associated with MRI and MRI CsPCa to generate corresponding risk scores and . was further generated by integrating and . Statistical significance was determined using the Wilcoxon signed-rank test.
Results: Both intra-lesional and peri-lesional bpMRI Haralick and CoLlAGe radiomic features were significantly associated with MRI CsPCa (p < 0.05). Intra-lesional ADC Haralick and CoLlAGe radiomic features were significantly different among MRI and MRI CsPCa (p < 0.05). yielded the highest AUC of 0.82 (95 % CI 0.72-0.91) compared to AUCs of 0.76 (95 % CI 0.63-0.89), and PI-RADS 0.58 (95 % CI 0.50-0.72) on D. correctly reclassified 10 out of 14 MRI CsPCa on D.
Conclusion: Our preliminary results demonstrated that both intra-lesional and peri-lesional bpMRI radiomic features were significantly associated with MRI CsPCa. These features could assist in CsPCa identification on bpMRI.
Mendes B, Domingues I, Santos J J Clin Med. 2024; 13(13).
PMID: 38999473 PMC: 11242211. DOI: 10.3390/jcm13133907.