4.6 Article

Impact of Lesion Delineation and Intensity Quantisation on the Stability of Texture Features from Lung Nodules on CT: A Reproducible Study

Journal

DIAGNOSTICS
Volume 11, Issue 7, Pages -

Publisher

MDPI
DOI: 10.3390/diagnostics11071224

Keywords

computed tomography; texture features; lung nodules; radiomics; lesion delineation; intensity quantisation; stability

Funding

  1. National Cancer Institute
  2. Foundation for the National Institutes of Health

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In this study, the stability of 88 texture features extracted from 517 lung lesions of lung cancer patients was assessed, with 30 features identified to have good or excellent stability in lesion delineation, 28 in intensity quantisation, and 18 in both aspects. Selecting the right set of imaging features is critical for building clinical predictive models, especially when changes in lesion delineation and/or intensity quantisation are involved.
Computer-assisted analysis of three-dimensional imaging data (radiomics) has received a lot of research attention as a possible means to improve the management of patients with lung cancer. Building robust predictive models for clinical decision making requires the imaging features to be stable enough to changes in the acquisition and extraction settings. Experimenting on 517 lung lesions from a cohort of 207 patients, we assessed the stability of 88 texture features from the following classes: first-order (13 features), Grey-level Co-Occurrence Matrix (24), Grey-level Difference Matrix (14), Grey-level Run-length Matrix (16), Grey-level Size Zone Matrix (16) and Neighbouring Grey-tone Difference Matrix (five). The analysis was based on a public dataset of lung nodules and open-access routines for feature extraction, which makes the study fully reproducible. Our results identified 30 features that had good or excellent stability relative to lesion delineation, 28 to intensity quantisation and 18 to both. We conclude that selecting the right set of imaging features is critical for building clinical predictive models, particularly when changes in lesion delineation and/or intensity quantisation are involved.

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