Stability of radiomics features in apparent diffusion coefficient maps from a multi-centre test-retest trial
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Authors
Peerlings, JWoodruff, H
Winfield, J
Ibrahim, A
Van Beers, B
Heerschap, A
Jackson, Andrew
Wildberger, J
Mottaghy, F
DeSouza, N
Lambin, P
Affiliation
The D-Lab, Department of Precision Medicine, Royal Marsden Hospital, Sutton, UKIssue Date
2019
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Quantitative radiomics features, extracted from medical images, characterize tumour-phenotypes and have been shown to provide prognostic value in predicting clinical outcomes. Stability of radiomics features extracted from apparent diffusion coefficient (ADC)-maps is essential for reliable correlation with the underlying pathology and its clinical applications. Within a multicentre, multi-vendor trial we established a method to analyse radiomics features from ADC-maps of ovarian (n?=?12), lung (n?=?19), and colorectal liver metastasis (n?=?30) cancer patients who underwent repeated (<7 days) diffusion-weighted imaging at 1.5?T and 3?T. From these ADC-maps, 1322 features describing tumour shape, texture and intensity were retrospectively extracted and stable features were selected using the concordance correlation coefficient (CCC?>?0.85). Although some features were tissue- and/or respiratory motion-specific, 122 features were stable for all tumour-entities. A large proportion of features were stable across different vendors and field strengths. By extracting stable phenotypic features, fitting-dimensionality is reduced and reliable prognostic models can be created, paving the way for clinical implementation of ADC-based radiomics.Citation
Peerlings J, Woodruff HC, Winfield JM, Ibrahim A, Van Beers BE, Heerschap A, et al. Stability of radiomics features in apparent diffusion coefficient maps from a multi-centre test-retest trial. Sci Rep. 2019 Mar 18;9(1):4800.Journal
Scientific ReportsDOI
10.1038/s41598-019-41344-5PubMed ID
30886309Additional Links
https://dx.doi.org/10.1038/s41598-019-41344-5Type
ArticleLanguage
enae974a485f413a2113503eed53cd6c53
10.1038/s41598-019-41344-5
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