4.7 Article

A Radio-genomics Approach for Identifying High Risk Estrogen Receptor-positive Breast Cancers on DCE-MRI: Preliminary Results in Predicting OncotypeDX Risk Scores

Journal

SCIENTIFIC REPORTS
Volume 6, Issue -, Pages -

Publisher

NATURE PORTFOLIO
DOI: 10.1038/srep21394

Keywords

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Funding

  1. National Science Foundation [IIP-1248316]
  2. National Cancer Institute of the National Institutes of Health [R01CA136535-01, R01CA140772-01, R21CA167811-01]
  3. National Institute of Biomedical Imaging and Bioengineering of the National Institutes of Health [R43EB015199-01]
  4. National Institute for Digestive Diseases and Kidney [R01DK098503]
  5. Case Comprehensive Cancer Center Support Grant [P30-CA043703]
  6. Case Western Reserve University
  7. V Foundation
  8. national natural science foundation of China [61401012]
  9. SRF for ROCS, SEM, China

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To identify computer extracted imaging features for estrogen receptor (ER)-positive breast cancers on dynamic contrast en-hanced (DCE)-MRI that are correlated with the low and high OncotypeDX risk categories. We collected 96 ER-positivebreast lesions with low (<18, N = 55) and high (>30, N = 41) OncotypeDX recurrence scores. Each lesion was quantitatively charac-terize via 6 shape features, 3 pharmacokinetics, 4 enhancement kinetics, 4 intensity kinetics, 148 textural kinetics, 5 dynamic histogram of oriented gradient (DHoG), and 6 dynamic local binary pattern (DLBP) features. The extracted features were evaluated by a linear discriminant analysis (LDA) classifier in terms of their ability to distinguish low and high OncotypeDX risk categories. Classification performance was evaluated by area under the receiver operator characteristic curve (Az). The DHoG and DLBP achieved Az values of 0.84 and 0.80, respectively. The 6 top features identified via feature selection were subsequently combined with the LDA classifier to yield an Az of 0.87. The correlation analysis showed that DHoG (rho = 0.85, P < 0.001) and DLBP (rho = 0.83, P < 0.01) were significantly associated with the low and high risk classifications from the OncotypeDX assay. Our results indicated that computer extracted texture features of DCE-MRI were highly correlated with the high and low OncotypeDX risk categories for ER-positive cancers.

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