In Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc
Differential classification of prostate cancer (CaP) grade group (GG) 2 and 3 tumors remains challenging, likely due to the subjective quantification of percentage of Gleason pattern 4 (%GP4). Artificial intelligence assessment of %GP4 may improve its accuracy and reproducibility and provide information for prognosis prediction. To investigate this potential, a convolutional neural network (CNN) model was trained to objectively identify and quantify Gleason pattern (GP) 3 and 4 areas, estimate %GP4, and assess whether CNN-assessed %GP4 is associated with biochemical recurrence (BCR) risk in intermediate risk GG 2 and 3 tumors. The study was conducted in a radical prostatectomy cohort (1999-2012) of African American men from the Henry Ford Health System (Detroit, Michigan). A CNN model that could discriminate four tissue types (stroma, benign glands, GP3 glands, and GP4 glands) was developed using histopathologic images containing GG 1 (n=45) and 4 (n=20) tumor foci. The CNN model was applied to GG 2 (n=153) and 3 (n=62) for %GP4 estimation, and Cox proportional hazard modeling was used to assess the association of %GP4 and BCR, accounting for other clinicopathologic features including GG. The CNN model achieved an overall accuracy of 86% in distinguishing the four tissue types. Further, CNN-assessed %GP4 was significantly higher in GG 3 compared with GG 2 tumors (p=7.2*10-11). %GP4 was associated with an increased risk of BCR (adjusted HR=1.09 per 10% increase in %GP4, p=0.010) in GG 2 and 3 tumors. Within GG 2 tumors specifically, %GP4 was more strongly associated with BCR (adjusted HR=1.12, p=0.006). Our findings demonstrate the feasibility of CNN-assessed %GP4 estimation, which is associated with BCR risk. This objective approach could be added to the standard pathological assessment for patients with GG 2 and 3 tumors and act as a surrogate for specialist genitourinary pathologist evaluation when such consultation is not available.
Chen Yalei, Loveless Ian M, Nakai Tiffany, Newaz Rehnuma, Abdollah Firas F, Rogers Craig G, Hassan Oudai, Chitale Dhananjay, Arora Kanika, Williamson Sean R, Gupta Nilesh S, Rybicki Benjamin A, Sadasivan Sudha M, Levin Albert M
2023-Mar-14
