4.7 Article

Quantitative glioma grading using transformed gray-scale invariant textures of MRI

Journal

COMPUTERS IN BIOLOGY AND MEDICINE
Volume 83, Issue -, Pages 102-108

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.compbiomed.2017.02.012

Keywords

Brain tumor; Glioma; Computer-aided diagnosis; Local binary pattern; Magnetic resonance imaging

Funding

  1. Ministry of Science and Technology, Taiwan [MOST 104-2218-E-038-004, MOST 103-2314-B-038-067, MOST 105-2314-B-038-049]
  2. Taipei Medical University [TMU 104-AE1-B04]

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Background: A computer-aided diagnosis (CAD) system based on intensity-invariant magnetic resonance (MR) imaging features was proposed to grade gliomas for general application to various scanning systems and settings. Method: In total, 34 glioblastomas and 73 lower-grade gliomas comprised the image database to evaluate the proposed CAD system. For each case, the local texture on MR images was transformed into a local binary pattern (LBP) which was intensity-invariant. From the LBP, quantitative image features, including the histogram moment and textures, were extracted and combined in a logistic regression classifier to establish a malignancy prediction model. The performance was compared to conventional texture features to demonstrate the improvement. Results: The performance of the CAD system based on LBP features achieved an accuracy of 93% (100/107), a sensitivity of 97% (33/34), a negative predictive value of 99% (67/68), and an area under the receiver operating characteristic curve (Az) of 0.94, which were significantly better than the conventional texture features: an accuracy of 84% (90/107), a sensitivity of 76% (26/34), a negative predictive value of 89% (64/72), and an Az of 0.89 with respective p values of 0.0303, 0.0122, 0.0201, and 0.0334. Conclusions: More-robust texture features were extracted from MR images and combined into a significantly better CAD system for distinguishing glioblastomas from lower-grade gliomas. The proposed CAD system would be more practical in clinical use with various imaging systems and settings.

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