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Automation of pattern recognition analysis of dynamic contrast-enhanced MRI data to characterize intratumoral vascular heterogeneity.
Han, SoHyun; Stoyanova, Radka; Lee, Hansol; Carlin, Sean D; Koutcher, Jason A; Cho, HyungJoon; Ackerstaff, Ellen.
Affiliation
  • Han S; Department of Biomedical Engineering, Ulsan National Institute of Science and Technology, Ulsan, South Korea.
  • Stoyanova R; Currently at: Center for Neuroscience Imaging Research, Institute for Basic Science (IBS), Suwon, South Korea.
  • Lee H; Department of Radiation Oncology, Miller School of Medicine, University of Miami, Miami, Florida, USA.
  • Carlin SD; Department of Biomedical Engineering, Ulsan National Institute of Science and Technology, Ulsan, South Korea.
  • Koutcher JA; Department of Medical Physics, Memorial Sloan Kettering Cancer Center, New York, New York, USA.
  • Cho H; Currently at: Department of Radiology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania, USA.
  • Ackerstaff E; Department of Medical Physics, Memorial Sloan Kettering Cancer Center, New York, New York, USA.
Magn Reson Med ; 79(3): 1736-1744, 2018 03.
Article in En | MEDLINE | ID: mdl-28727185
PURPOSE: To automate dynamic contrast-enhanced MRI (DCE-MRI) data analysis by unsupervised pattern recognition (PR) to enable spatial mapping of intratumoral vascular heterogeneity. METHODS: Three steps were automated. First, the arrival time of the contrast agent at the tumor was determined, including a calculation of the precontrast signal. Second, four criteria-based algorithms for the slice-specific selection of number of patterns (NP) were validated using 109 tumor slices from subcutaneous flank tumors of five different tumor models. The criteria were: half area under the curve, standard deviation thresholding, percent signal enhancement, and signal-to-noise ratio (SNR). The performance of these criteria was assessed by comparing the calculated NP with the visually determined NP. Third, spatial assignment of single patterns and/or pattern mixtures was obtained by way of constrained nonnegative matrix factorization. RESULTS: The determination of the contrast agent arrival time at the tumor slice was successfully automated. For the determination of NP, the SNR-based approach outperformed other selection criteria by agreeing >97% with visual assessment. The spatial localization of single patterns and pattern mixtures, the latter inferring tumor vascular heterogeneity at subpixel spatial resolution, was established successfully by automated assignment from DCE-MRI signal-versus-time curves. CONCLUSION: The PR-based DCE-MRI analysis was successfully automated to spatially map intratumoral vascular heterogeneity. Magn Reson Med 79:1736-1744, 2018. © 2017 International Society for Magnetic Resonance in Medicine.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Pattern Recognition, Automated / Magnetic Resonance Imaging / Image Interpretation, Computer-Assisted / Neoplasms / Neovascularization, Pathologic Type of study: Prognostic_studies Limits: Humans Language: En Journal: Magn Reson Med Journal subject: DIAGNOSTICO POR IMAGEM Year: 2018 Document type: Article Affiliation country: Korea (South) Country of publication: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Pattern Recognition, Automated / Magnetic Resonance Imaging / Image Interpretation, Computer-Assisted / Neoplasms / Neovascularization, Pathologic Type of study: Prognostic_studies Limits: Humans Language: En Journal: Magn Reson Med Journal subject: DIAGNOSTICO POR IMAGEM Year: 2018 Document type: Article Affiliation country: Korea (South) Country of publication: United States