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Findings of Dti-P Maps in Comparison With T 2 /T 2 -Flair to Assess Postoperative Hyper-Signal Abnormal Regions in Patients With Glioblastoma 08 Information and Computing Sciences 0801 Artificial Intelligence and Image Processing Publisher Pubmed



Beigi M1 ; Safari M2 ; Ameri A3 ; Moghadam MS4 ; Arbabi A5 ; Tabatabaeefar M3 ; Salighehrad H1
Authors
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Authors Affiliations
  1. 1. Quantitative MR Imaging and Spectroscopy Group, Research Center for Cellular and Molecular Imaging, Institute for Advanced Medical Imaging, Department of Medical Physics and Biomedical Engineering, Tehran University of Medical Sciences, Tehran, Iran
  2. 2. Department of Energy Engineering, Sharif University of Technology, Tehran, Iran
  3. 3. Department of Clinical Oncology, Shahid Beheshti University of Medical Science, Tehran, Iran
  4. 4. Payambaran Imaging Center, Tehran, Iran
  5. 5. Department of Medical Physics, Shahid Beheshti University of Medical Science, Tehran, Iran

Source: Cancer Imaging Published:2018


Abstract

Purpose: The aim of this study was to compare diffusion tensor imaging (DTI) isotropic map (p-map) with current radiographically (T 2/T 2 -FLAIR) methods based on abnormal hyper-signal size and location of glioblastoma tumor using a semi-automatic approach. Materials and methods: Twenty-five patients with biopsy-proved diagnosis of glioblastoma participated in this study. T 2, T 2 -FLAIR images and diffusion tensor imaging (DTI) were acquired 1 week before radiotherapy. Hyper-signal regions on T 2, T 2 -FLAIR and DTI p-map were segmented by means of semi-automated segmentation. Manual segmentation was used as ground truth. Dice Scores (DS) were calculated for validation of semiautomatic method. Discordance Index (DI) and area difference percentage between the three above regions from the three modalities were calculated for each patient. Results: Area of abnormality in the p-map was smaller than the corresponding areas in the T 2 and T 2 -FLAIR images in 17 patients; with mean difference percentage of 30 ± 0.15 and 35 ± 0.15, respectively. Abnormal region in the p-map was larger than the corresponding areas in the T 2 -FLAIR and T 2 images in 4 patients; with mean difference percentage of 26 ± 0.17 and 29 ± 0.28, respectively. This region in the p-map was larger than the one in the T 2 image and smaller than the one in the T 2 -FLAIR image in 3 patients; with mean difference percentage of 34 ± 0.08 and 27 ± 0.06, respectively. Lack of concordance was observed ranged from 0.214-0.772 for T 2 -FLAIR/p-map (average: 0.462 ± 0.18), 0.266-0.794 for T 2 /p-map (average: 0.468 ± 0.13) and 0.123-0.776 for T 2 / T 2 -FLAIR (average: 0.423 ± 0.2). These regions on three modalities were segmented using a semi-automatic segmentation method with over 86% sensitivity, 90% specificity and 89% dice score for three modalities. Conclusion: It is noted that T 2, T 2 -FLAIR and DTI p-maps represent different but complementary information for delineation of glioblastoma tumor margins. Therefore, this study suggests DTI p-map modality as a candidate to improve target volume delineation based on conventional modalities, which needs further investigations with follow-up data to be confirmed. © 2018 The Author(s).