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Semi-automated segmentation of pre-operative low grade gliomas in magnetic resonance imaging
Z. Akkus, J. Sedlar, L. Coufalova, P. Korfiatis, TL. Kline, JD. Warner, J. Agrawal, BJ. Erickson,
Language English Country England, Great Britain
Document type Journal Article, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't
NLK
BioMedCentral
from 2000-06-01
BioMedCentral Open Access
from 2014
Directory of Open Access Journals
from 2014
Free Medical Journals
from 2004 to 2 years ago
PubMed Central
from 2000
Europe PubMed Central
from 2000
ProQuest Central
from 2015-01-01
Open Access Digital Library
from 2000-01-01
Open Access Digital Library
from 2014-01-01
Medline Complete (EBSCOhost)
from 2008-01-02
Health & Medicine (ProQuest)
from 2015-01-01
Health Management Database (ProQuest)
from 2015-01-01
ROAD: Directory of Open Access Scholarly Resources
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Springer Nature OA/Free Journals
from 2000-06-01
- MeSH
- Algorithms MeSH
- Glioma pathology surgery MeSH
- Humans MeSH
- Magnetic Resonance Imaging * methods MeSH
- Brain Neoplasms pathology surgery MeSH
- Image Processing, Computer-Assisted * MeSH
- Sensitivity and Specificity MeSH
- Check Tag
- Humans MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Research Support, N.I.H., Extramural MeSH
BACKGROUND: Segmentation of pre-operative low-grade gliomas (LGGs) from magnetic resonance imaging is a crucial step for studying imaging biomarkers. However, segmentation of LGGs is particularly challenging because they rarely enhance after gadolinium administration. Like other gliomas, they have irregular tumor shape, heterogeneous composition, ill-defined tumor boundaries, and limited number of image types. To overcome these challenges we propose a semi-automated segmentation method that relies only on T2-weighted (T2W) and optionally post-contrast T1-weighted (T1W) images. METHODS: First, the user draws a region-of-interest (ROI) that completely encloses the tumor and some normal tissue. Second, a normal brain atlas and post-contrast T1W images are registered to T2W images. Third, the posterior probability of each pixel/voxel belonging to normal and abnormal tissues is calculated based on information derived from the atlas and ROI. Finally, geodesic active contours use the probability map of the tumor to shrink the ROI until optimal tumor boundaries are found. This method was validated against the true segmentation (TS) of 30 LGG patients for both 2D (1 slice) and 3D. The TS was obtained from manual segmentations of three experts using the Simultaneous Truth and Performance Level Estimation (STAPLE) software. Dice and Jaccard indices and other descriptive statistics were computed for the proposed method, as well as the experts' segmentation versus the TS. We also tested the method with the BraTS datasets, which supply expert segmentations. RESULTS AND DISCUSSION: For 2D segmentation vs. TS, the mean Dice index was 0.90 ± 0.06 (standard deviation), sensitivity was 0.92, and specificity was 0.99. For 3D segmentation vs. TS, the mean Dice index was 0.89 ± 0.06, sensitivity was 0.91, and specificity was 0.99. The automated results are comparable with the experts' manual segmentation results. CONCLUSIONS: We present an accurate, robust, efficient, and reproducible segmentation method for pre-operative LGGs.
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- $a BACKGROUND: Segmentation of pre-operative low-grade gliomas (LGGs) from magnetic resonance imaging is a crucial step for studying imaging biomarkers. However, segmentation of LGGs is particularly challenging because they rarely enhance after gadolinium administration. Like other gliomas, they have irregular tumor shape, heterogeneous composition, ill-defined tumor boundaries, and limited number of image types. To overcome these challenges we propose a semi-automated segmentation method that relies only on T2-weighted (T2W) and optionally post-contrast T1-weighted (T1W) images. METHODS: First, the user draws a region-of-interest (ROI) that completely encloses the tumor and some normal tissue. Second, a normal brain atlas and post-contrast T1W images are registered to T2W images. Third, the posterior probability of each pixel/voxel belonging to normal and abnormal tissues is calculated based on information derived from the atlas and ROI. Finally, geodesic active contours use the probability map of the tumor to shrink the ROI until optimal tumor boundaries are found. This method was validated against the true segmentation (TS) of 30 LGG patients for both 2D (1 slice) and 3D. The TS was obtained from manual segmentations of three experts using the Simultaneous Truth and Performance Level Estimation (STAPLE) software. Dice and Jaccard indices and other descriptive statistics were computed for the proposed method, as well as the experts' segmentation versus the TS. We also tested the method with the BraTS datasets, which supply expert segmentations. RESULTS AND DISCUSSION: For 2D segmentation vs. TS, the mean Dice index was 0.90 ± 0.06 (standard deviation), sensitivity was 0.92, and specificity was 0.99. For 3D segmentation vs. TS, the mean Dice index was 0.89 ± 0.06, sensitivity was 0.91, and specificity was 0.99. The automated results are comparable with the experts' manual segmentation results. CONCLUSIONS: We present an accurate, robust, efficient, and reproducible segmentation method for pre-operative LGGs.
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