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dc.contributor.authorVidic, Igor
dc.contributor.authorEgnell, Liv
dc.contributor.authorJerome, Neil Peter
dc.contributor.authorTeruel, Jose Ramon
dc.contributor.authorSjøbakk, Torill Eidhammer
dc.contributor.authorØstlie, Agnes
dc.contributor.authorFjøsne, Hans Erikssønn
dc.contributor.authorBathen, Tone Frost
dc.contributor.authorGoa, Pål Erik
dc.date.accessioned2018-02-26T13:51:28Z
dc.date.available2018-02-26T13:51:28Z
dc.date.created2017-12-20T13:31:35Z
dc.date.issued2017
dc.identifier.issn1053-1807
dc.identifier.urihttp://hdl.handle.net/11250/2487052
dc.description.abstractBackground Diffusion-weighted MRI (DWI) is currently one of the fastest developing MRI-based techniques in oncology. Histogram properties from model fitting of DWI are useful features for differentiation of lesions, and classification can potentially be improved by machine learning. Purpose To evaluate classification of malignant and benign tumors and breast cancer subtypes using support vector machine (SVM). Study Type Prospective. SUBJECTS Fifty-one patients with benign (n = 23) and malignant (n = 28) breast tumors (26 ER+, whereof six were HER2+). Field Strength/Sequence Patients were imaged with DW-MRI (3T) using twice refocused spin-echo echo-planar imaging with echo time / repetition time (TR/TE) = 9000/86 msec, 90 × 90 matrix size, 2 × 2 mm in-plane resolution, 2.5 mm slice thickness, and 13 b-values. Assessment Apparent diffusion coefficient (ADC), relative enhanced diffusivity (RED), and the intravoxel incoherent motion (IVIM) parameters diffusivity (D), pseudo-diffusivity (D*), and perfusion fraction (f) were calculated. The histogram properties (median, mean, standard deviation, skewness, kurtosis) were used as features in SVM (10-fold cross-validation) for differentiation of lesions and subtyping. Statistical Tests Accuracies of the SVM classifications were calculated to find the combination of features with highest prediction accuracy. Mann–Whitney tests were performed for univariate comparisons. Results For benign versus malignant tumors, univariate analysis found 11 histogram properties to be significant differentiators. Using SVM, the highest accuracy (0.96) was achieved from a single feature (mean of RED), or from three feature combinations of IVIM or ADC. Combining features from all models gave perfect classification. No single feature predicted HER2 status of ER + tumors (univariate or SVM), although high accuracy (0.90) was achieved with SVM combining several features. Importantly, these features had to include higher-order statistics (kurtosis and skewness), indicating the importance to account for heterogeneity. Data Conclusion Our findings suggest that SVM, using features from a combination of diffusion models, improves prediction accuracy for differentiation of benign versus malignant breast tumors, and may further assist in subtyping of breast cancer. Level of Evidence: 3 Technical Efficacy: Stage 3nb_NO
dc.language.isoengnb_NO
dc.publisherWileynb_NO
dc.titleSupport vector machine for breast cancer classification using diffusion-weighted MRI histogram features: Preliminary study.nb_NO
dc.typeJournal articlenb_NO
dc.description.versionsubmittedVersionnb_NO
dc.source.journalJournal of Magnetic Resonance Imagingnb_NO
dc.identifier.doi10.1002/jmri.25873
dc.identifier.cristin1530416
dc.relation.projectNorges forskningsråd: 221879nb_NO
dc.description.localcodeThis is the pre-peer reviewed version of the following article: [Support vector machine for breast cancer classification using diffusion-weighted MRI histogram features: Preliminary study], which has been published in final form at [http://onlinelibrary.wiley.com/doi/10.1002/jmri.25873/abstract]. This article may be used for non-commercial purposes in accordance with Wiley Terms and Conditions for Self-Archiving.nb_NO
cristin.unitcode194,66,20,0
cristin.unitcode194,65,25,0
cristin.unitcode194,65,15,0
cristin.unitnameInstitutt for fysikk
cristin.unitnameInstitutt for sirkulasjon og bildediagnostikk
cristin.unitnameInstitutt for klinisk og molekylær medisin
cristin.ispublishedfalse
cristin.fulltextpreprint
cristin.qualitycode2


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