Deep Learning of Rhabdomyosarcoma Pathology Images for Classification and Survival Outcome Prediction.

Journal: The American journal of pathology
Published Date:

Abstract

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.

Authors

  • Xinyi Zhang
    Department of Gastroenterology, The First Affiliated Hospital of Zhejiang Chinese Medical University, Hangzhou, China.
  • Shidan Wang
    Quantitative Biomedical Research Center, Department of Clinical Sciences, University of Texas Southwestern Medical Center, 5325 Harry Hines Blvd, Dallas, TX, 75390, USA.
  • Erin R Rudzinski
    Division of Anatomic Pathology, Seattle Children's Hospital, Seattle, Washington.
  • Saloni Agarwal
    University of Texas at Dallas, Richardson, TX.
  • Ruichen Rong
    Quantitative Biomedical Research Center, Department of Population and Data Sciences, University of Texas Southwestern Medical Center, Dallas, Texas.
  • Donald A Barkauskas
    Department of Population and Public Health Sciences, Keck School of Medicine of the University of Southern California, Los Angeles, California.
  • Ovidiu Daescu
    1 Department of Computer Science, University of Texas at Dallas , Richardson, Texas.
  • Lauren Furman Cline
    Division of Pediatric Hematology and Oncology, Department of Pediatrics, University of Texas Southwestern Medical Center, Dallas, Texas.
  • Rajkumar Venkatramani
    Department of Pediatrics, Baylor College of Medicine, Houston, Texas; Oncology Section, Texas Children's Hospital, Houston, Texas.
  • Yang Xie
    Quantitative Biomedical Research Center, Department of Clinical Sciences, University of Texas Southwestern Medical Center, 5325 Harry Hines Blvd, Dallas, TX, 75390, USA.
  • Guanghua Xiao
  • Patrick Leavey
    2 University of Texas Southwestern Medical Center , Dallas, Texas.