Abstract

ObjectivesTo develop an automatic method for identification and segmentation of clinically significant prostate cancer in low-risk patients and to evaluate the performance in a routine clinical setting.MethodsA consecutive cohort (n = 292) from a prospective database of low-risk patients eligible for the active surveillance was selected. A 3-T multi-parametric MRI at 3 months after inclusion was performed. Histopathology from biopsies was used as reference standard. MRI positivity was defined as PI-RADS score ≥ 3, histopathology positivity was defined as ISUP grade ≥ 2. The selected cohort contained four patient groups: (1) MRI-positive targeted biopsy-positive (n = 116), (2) MRI-negative systematic biopsy-negative (n = 55), (3) MRI-positive targeted biopsy-negative (n = 113), (4) MRI-negative systematic biopsy-positive (n = 8). Group 1 was further divided into three sets and a 3D convolutional neural network was trained using different combinations of these sets. Two MRI sequences (T2w, b = 800 DWI) and the ADC map were used as separate input channels for the model. After training, the model was evaluated on the remaining group 1 patients together with the patients of groups 2 and 3 to identify and segment clinically significant prostate cancer.ResultsThe average sensitivity achieved was 82–92% at an average specificity of 43–76% with an area under the curve (AUC) of 0.65 to 0.89 for different lesion volumes ranging from > 0.03 to > 0.5 cc.ConclusionsThe proposed deep learning computer-aided method yields promising results in identification and segmentation of clinically significant prostate cancer and in confirming low-risk cancer (ISUP grade ≤ 1) in patients on active surveillance.Key Points• Clinically significant prostate cancer identification and segmentation on multi-parametric MRI is feasible in low-risk patients using a deep neural network.• The deep neural network for significant prostate cancer localization performs better for lesions with larger volumes sizes (> 0.5 cc) as compared to small lesions (> 0.03 cc).• For the evaluation of automatic prostate cancer segmentation methods in the active surveillance cohort, the large discordance group (MRI positive, targeted biopsy negative) should be included.

Highlights

  • The standard clinical procedure for diagnosing prostate cancer (PCa) is a systematic transrectal ultrasound-guided (TRUS) biopsy, indicated by an elevated prostate-specific antigen (PSA) level and/or an abnormal digital rectal examination (DRE) [1]. This procedure results in low sensitivity and specificity [2, 3] leading to underdiagnosis of clinically significant PCa and overdiagnosis of insignificant PCa

  • The division of patients into the different ISUP grade groups and their relation with the assigned PIRADS score (Fig. 4a) show that many patients (n = 101) were scored Prostate Imaging Reporting and Data System (PI-RADS) ≥ 3 by the radiologist but these patients had no significant PCa based on targeted biopsies

  • Some patients (n = 8) were assigned PI-RADS score ≤ 2 and had significant PCa based on the systematic biopsies procedure

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Summary

Introduction

The standard clinical procedure for diagnosing prostate cancer (PCa) is a systematic transrectal ultrasound-guided (TRUS) biopsy, indicated by an elevated prostate-specific antigen (PSA) level and/or an abnormal digital rectal examination (DRE) [1]. This procedure results in low sensitivity and specificity [2, 3] leading to underdiagnosis of clinically significant PCa and overdiagnosis of insignificant PCa. Recently, multi-parametric magnetic resonance imaging (mpMRI) has been reported as a more accurate alternative for PCa characterization and detection [4,5,6]. It may contribute in improving the diagnostic chain [11] and thereby reducing over- and underdiagnosis and treatment in prostate cancer management [10]

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