Training robust T1-weighted magnetic resonance imaging liver segmentation models using ensembles of datasets with different contrast protocols and liver disease etiologies.

Journal: Scientific reports
Published Date:

Abstract

Image segmentation of the liver is an important step in treatment planning for liver cancer. However, manual segmentation at a large scale is not practical, leading to increasing reliance on deep learning models to automatically segment the liver. This manuscript develops a generalizable deep learning model to segment the liver on T1-weighted MR images. In particular, three distinct deep learning architectures (nnUNet, PocketNet, Swin UNETR) were considered using data gathered from six geographically different institutions. A total of 819 T1-weighted MR images were gathered from both public and internal sources. Our experiments compared each architecture's testing performance when trained both intra-institutionally and inter-institutionally. Models trained using nnUNet and its PocketNet variant achieved mean Dice-Sorensen similarity coefficients>0.9 on both intra- and inter-institutional test set data. The performance of these models suggests that nnUNet and PocketNet liver segmentation models trained on a large and diverse collection of T1-weighted MR images would on average achieve good intra-institutional segmentation performance.

Authors

  • Nihil Patel
    Department of Imaging Physics, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
  • Adrian Celaya
    Department of Imaging Physics, MD Anderson Cancer Center, The University of Texas, Houston, Texas, USA.
  • Mohamed Eltaher
    Department of Imaging Physics, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
  • Rachel Glenn
    Department of Imaging Physics, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
  • Kari Brewer Savannah
    Department of Imaging Physics, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
  • Kristy K Brock
    Department of Imaging Physics, The University of Texas MD Anderson Cancer Center, Houston, Texas; Department of Radiation Physics, The University of Texas MD Anderson Cancer Center, Houston, Texas.
  • Jessica I Sanchez
    Department of Molecular and Cellular Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
  • Tiffany L Calderone
    Department of Molecular and Cellular Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
  • Darrel Cleere
    Department of Gastroenterology, Houston Methodist Hospital, Houston, Texas, USA.
  • Ahmed Elsaiey
    Department of Gastroenterology, Houston Methodist Hospital, Houston, Texas, USA.
  • Matthew Cagley
    Department of Radiation Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
  • Nakul Gupta
    Department of Radiology, Houston Methodist Hospital, Houston, Texas, USA.
  • David Victor
    JC Walter Jr Transplant Center, Houston Methodist Hospital, Houston, TX, 77030, United States; Department of Medicine, Houston Methodist Hospital, Houston, TX, 77030, United States.
  • Laura Beretta
    Department of Molecular and Cellular Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
  • Eugene J Koay
    Department of Radiation Oncology, MD Anderson Cancer Center, Houston, Texas.
  • Tucker J Netherton
    Department of Radiation Physics, The University of Texas MD Anderson Cancer Center, Houston, TX, 77030, USA.
  • David T Fuentes
    Department of Imaging Physics, Division of Diagnostic Imaging, The University of Texas MD Anderson Cancer Center, Houston, TX.