4.7 Article

Robustness of radiomic features in CT images with different slice thickness, comparing liver tumour and muscle

Journal

SCIENTIFIC REPORTS
Volume 11, Issue 1, Pages -

Publisher

NATURE PORTFOLIO
DOI: 10.1038/s41598-021-87598-w

Keywords

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Funding

  1. CRUK National Cancer Imaging Translational Accelerator (NCITA) [C42780/A27066]
  2. Cancer Research UK (CRUK) Cambridge Centre [C9685/A25177]
  3. CRUK-OHSU Early Detection Project Award [C52489/A29681]
  4. CRUK HCC Accelerator Award [C18873/A26813]
  5. Academy of Medical Sciences
  6. Wellcome Trust
  7. Medical Research Council (MRC)
  8. British Heart Foundation
  9. Versus Arthritis
  10. Diabetes UK
  11. British Thoracic Society [SGL019/1007]
  12. National Institute of Health Research (NIHR) Cambridge Biomedical Research Centre [BRC-1215-20014]
  13. Wellcome Trust Innovator Award [RG98755]
  14. Mark Foundation for Cancer Research

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This study evaluated the robustness of radiomic features extracted from CT images, comparing feature values in images of different thicknesses and using novel approaches to address dependencies, resulting in the discovery of highly robust features across different thicknesses.
Radiomic image features are becoming a promising non-invasive method to obtain quantitative measurements for tumour classification and therapy response assessment in oncological research. However, despite its increasingly established application, there is a need for standardisation criteria and further validation of feature robustness with respect to imaging acquisition parameters. In this paper, the robustness of radiomic features extracted from computed tomography (CT) images is evaluated for liver tumour and muscle, comparing the values of the features in images reconstructed with two different slice thicknesses of 2.0 mm and 5.0 mm. Novel approaches are presented to address the intrinsic dependencies of texture radiomic features, choosing the optimal number of grey levels and correcting for the dependency on volume. With the optimal values and corrections, feature values are compared across thicknesses to identify reproducible features. Normalisation using muscle regions is also described as an alternative approach. With either method, a large fraction of features (75-90%) was found to be highly robust (< 25% difference). The analyses were performed on a homogeneous CT dataset of 43 patients with hepatocellular carcinoma, and consistent results were obtained for both tumour and muscle tissue. Finally, recommended guidelines are included for radiomic studies using variable slice thickness.

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