Novel PCA-VIP scheme for ranking MRI protocols and identifying computer-extracted MRI measurements associated with central gland and peripheral zone prostate tumors

Purpose To identify computer‐extracted features for central gland and peripheral zone prostate cancer localization on multiparametric magnetic resonance imaging (MRI). Materials and Methods Preoperative T2‐weighted (T2w), diffusion‐weighted imaging (DWI), and dynamic contrast‐enhanced (DCE) MRI were...

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Published inJournal of magnetic resonance imaging Vol. 41; no. 5; pp. 1383 - 1393
Main Authors Ginsburg, Shoshana B., Viswanath, Satish E., Bloch, B. Nicolas, Rofsky, Neil M., Genega, Elizabeth M., Lenkinski, Robert E., Madabhushi, Anant
Format Journal Article
LanguageEnglish
Published United States Blackwell Publishing Ltd 01.05.2015
Wiley Subscription Services, Inc
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Summary:Purpose To identify computer‐extracted features for central gland and peripheral zone prostate cancer localization on multiparametric magnetic resonance imaging (MRI). Materials and Methods Preoperative T2‐weighted (T2w), diffusion‐weighted imaging (DWI), and dynamic contrast‐enhanced (DCE) MRI were acquired from 23 men with confirmed prostate cancer. Following radical prostatectomy, the cancer extent was delineated by a pathologist on ex vivo histology and mapped to MRI by nonlinear registration of histology and corresponding MRI slices. In all, 244 computer‐extracted features were extracted from MRI, and principal component analysis (PCA) was employed to reduce the data dimensionality so that a generalizable classifier could be constructed. A novel variable importance on projection (VIP) measure for PCA (PCA‐VIP) was leveraged to identify computer‐extracted MRI features that discriminate between cancer and normal prostate, and these features were used to construct classifiers for cancer localization. Results Classifiers using features selected by PCA‐VIP yielded an area under the curve (AUC) of 0.79 and 0.85 for peripheral zone and central gland tumors, respectively. For tumor localization in the central gland, T2w, DCE, and DWI MRI features contributed 71.6%, 18.1%, and 10.2%, respectively; for peripheral zone tumors T2w, DCE, and DWI MRI contributed 29.6%, 21.7%, and 48.7%, respectively. Conclusion PCA‐VIP identified relatively stable subsets of MRI features that performed well in localizing prostate cancer on MRI. J. Magn. Reson. Imaging 2015;41:1383–1393. © 2014 Wiley Periodicals, Inc.
Bibliography:istex:149E52D4802074483440C6A85EB9D82A99EB56DB
National Institute of Biomedical Imaging and Bioengineering of the National Institutes of Health - No. R43EB015199-01
ark:/67375/WNG-19SKSZMZ-B
ArticleID:JMRI24676
National Cancer Institute of the National Institutes of Health - No. R01CA136535-01, R01CA140772-01, and R21CA167811-01
National Science Foundation - No. IIP-1248316
University City Science Center and Rutgers University
National Science Foundation Graduate Research Fellowship
Supported by the National Cancer Institute of the National Institutes of Health under award numbers R01CA136535‐01, R01CA140772‐01, and R21CA167811‐01; the National Institute of Biomedical Imaging and Bioengineering of the National Institutes of Health under award number R43EB015199‐01; the National Science Foundation under award number IIP‐1248316; the QED award from the University City Science Center and Rutgers University; and the National Science Foundation Graduate Research Fellowship.
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ISSN:1053-1807
1522-2586
1522-2586
DOI:10.1002/jmri.24676