TY - JOUR
T1 - Deep Learning of Rhabdomyosarcoma Pathology Images for Classification and Survival Outcome Prediction
AU - Zhang, Xinyi
AU - Wang, Shidan
AU - Rudzinski, Erin R.
AU - Agarwal, Saloni
AU - Rong, Ruichen
AU - Barkauskas, Donald A.
AU - Daescu, Ovidiu
AU - Furman Cline, Lauren
AU - Venkatramani, Rajkumar
AU - Xie, Yang
AU - Xiao, Guanghua
AU - Leavey, Patrick
N1 - Publisher Copyright:
Copyright © 2022 American Society for Investigative Pathology. Published by Elsevier Inc. All rights reserved.
PY - 2022/6/1
Y1 - 2022/6/1
N2 - Rhabdomyosarcoma (RMS), the most common malignant soft tissue tumor in children, has several histologic subtypes that influence treatment and predict patient outcomes. Assistance with histologic classification for pathologists as well as discovery of optimized predictive biomarkers is needed. A convolutional neural network for RMS histology subtype classification was developed using digitized pathology images from 80 patients collected at time of diagnosis. A subsequent embryonal rhabdomyosarcoma (eRMS) prognostic model was also developed in a cohort of 60 eRMS patients. The RMS classification model reached a performance of an area under the receiver operating curve of 0.94 for alveolar rhabdomyosarcoma and an area under the receiver operating curve of 0.92 for eRMS at slide level in the test data set (n = 192). The eRMS prognosis model separated the patients into predicted high- and low-risk groups with significantly different event-free survival outcome (likelihood ratio test; P = 0.02) in the test data set (n = 136). The predicted risk group is significantly associated with patient event-free survival outcome after adjusting for patient age and sex (predicted high- versus low-risk group hazard ratio, 4.64; 95% CI, 1.05-20.57; P = 0.04). This is the first comprehensive study to develop computational algorithms for subtype classification and prognosis prediction for RMS histopathology images. Such models can aid pathology evaluation and provide additional parameters for risk stratification.
AB - Rhabdomyosarcoma (RMS), the most common malignant soft tissue tumor in children, has several histologic subtypes that influence treatment and predict patient outcomes. Assistance with histologic classification for pathologists as well as discovery of optimized predictive biomarkers is needed. A convolutional neural network for RMS histology subtype classification was developed using digitized pathology images from 80 patients collected at time of diagnosis. A subsequent embryonal rhabdomyosarcoma (eRMS) prognostic model was also developed in a cohort of 60 eRMS patients. The RMS classification model reached a performance of an area under the receiver operating curve of 0.94 for alveolar rhabdomyosarcoma and an area under the receiver operating curve of 0.92 for eRMS at slide level in the test data set (n = 192). The eRMS prognosis model separated the patients into predicted high- and low-risk groups with significantly different event-free survival outcome (likelihood ratio test; P = 0.02) in the test data set (n = 136). The predicted risk group is significantly associated with patient event-free survival outcome after adjusting for patient age and sex (predicted high- versus low-risk group hazard ratio, 4.64; 95% CI, 1.05-20.57; P = 0.04). This is the first comprehensive study to develop computational algorithms for subtype classification and prognosis prediction for RMS histopathology images. Such models can aid pathology evaluation and provide additional parameters for risk stratification.
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U2 - 10.1016/j.ajpath.2022.03.011
DO - 10.1016/j.ajpath.2022.03.011
M3 - Article
C2 - 35390316
AN - SCOPUS:85131770908
SN - 0002-9440
VL - 192
SP - 917
EP - 925
JO - American Journal of Pathology
JF - American Journal of Pathology
IS - 6
ER -