Precise segmentation of rectal cancer tumors on routine MRI is critical for accurate clinical staging and downstream computational analyses. While deep learning-based segmentation algorithms have shown much promise in automating the otherwise tedious, subjective, and costly process of manual segmentation, they require significant amounts of manually annotated data for training. To address these limitations of deep learning-based segmentation models, we present a novel deep learning framework that incorporates human-in-the-loop (HITL) refinement to automatically delineate rectal tumors on multi-plane pre-treatment MR imaging. When evaluated on multiple holdout validation cohorts including a clinical trial dataset, the post-HITL segmentation model significantly outperformed the pre-HITL model with median dice similarity coefficient of 0.763 and Hausdorff distance of 28.4mm in comparison to 0.601 and 31.8mm, respectively. HITL refinement learning also significantly accelerated the manual annotation process by 20 minutes. HITL learning represents a feasible, effective, and efficient solution to semi-automated tumor segmentation on routine rectal cancer MRI scans.
Multiparametric magnetic resonance imaging (MP-MRI), including diffusion-weighted imaging, is commonly used to diagnose prostate cancer. This radiology–pathology study correlates prostate cancer grade and morphology with common b-value combinations for calculating apparent diffusion coefficient (ADC). Thirty-nine patients undergoing radical prostatectomy were recruited for MP-MRI prior to surgery. Diffusion imaging was collected with seven b-values, and ADC was calculated. Excised prostates were sliced in the same orientation as the MRI using 3-D printed slicing jigs. Whole-mount slides were digitized and annotated by a pathologist. Annotated samples were aligned to the MRI, and ADC values were extracted from annotated peripheral zone (PZ) regions. A receiver operating characteristic (ROC) analysis was performed to determine accuracy of tissue type discrimination and optimal ADC b-value combination. ADC significantly discriminates Gleason (G) G4-5 cancer from G3 and other prostate tissue types. The optimal b-values for discriminating high from low-grade and noncancerous tissue in the PZ are 50 and 2000, followed closely by 100 to 2000 and 0 to 2000. Optimal ADC cut-offs are presented for dichotomized discrimination of tissue types according to each b-value combination. Selection of b-values affects the sensitivity and specificity of ADC for discrimination of prostate cancer.
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