Segmentation of malignant gliomas through remote collaboration and statistical fusion
Purpose: Malignant gliomas represent an aggressive class of central nervous system neoplasms. Correlation of interventional outcomes with tumor morphometry data necessitates 3D segmentation of tumors (typically based on magnetic resonance imaging). Expert delineation is the long-held gold standard f...
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Published in | Medical physics (Lancaster) Vol. 39; no. 10; pp. 5981 - 5989 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
Published |
United States
American Association of Physicists in Medicine
01.10.2012
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Subjects | |
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Abstract | Purpose:
Malignant gliomas represent an aggressive class of central nervous system neoplasms. Correlation of interventional outcomes with tumor morphometry data necessitates 3D segmentation of tumors (typically based on magnetic resonance imaging). Expert delineation is the long-held gold standard for tumor segmentation, but is exceptionally resource intensive and subject to intrarater and inter-rater variability. Automated tumor segmentation algorithms have been demonstrated for a variety of imaging modalities and tumor phenotypes, but translation of these methods across clinical study designs is problematic given variation in image acquisition, tumor characteristics, segmentation objectives, and validation criteria. Herein, the authors demonstrate an alternative approach for high-throughput tumor segmentation using Internet-based, collaborative labeling.
Methods:
In a study of 85 human raters and 98 tumor patients, raters were recruited from a general university campus population (i.e., no specific medical knowledge), given minimal training, and provided web-based tools to label MRI images based on 2D cross sections. The labeling goal was characterized as to extract the enhanced tumor cores on T1-weighted MRI and the bright abnormality on T2-weighted MRI. An experienced rater manually constructed the ground truth volumes of a randomly sampled subcohort of 48 tumor subjects (for both T1w and T2w). Raters’ taskwise individual observations, as well as the volumewise truth estimates via statistical fusion method, were evaluated over the subjects having the ground truth.
Results:
Individual raters were able to reliably characterize (with >0.8 dice similarity coefficient, DSC) the gadolinium-enhancing cores and extent of the edematous areas only slightly more than half of the time. Yet, human raters were efficient in terms of providing these highly variable segmentations (less than 20 s per slice). When statistical fusion was used to combine the results of seven raters per slice for all slices in the datasets, the 3D agreement of the fused results with expertly delineated segmentations was on par with the inter-rater reliability observed between experienced raters using traditional 3D tools (approximately 0.85 DSC). The cumulative time spent per tumor patient with the collaborative approach was equivalent to that with an experienced rater, but the collaborative approach could be achieved with less training time, fewer resources, and efficient parallelization.
Conclusions:
Hence, collaborative labeling is a promising technique with potentially wide applicability to cost-effective manual labeling of medical images. |
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AbstractList | Purpose:
Malignant gliomas represent an aggressive class of central nervous system neoplasms. Correlation of interventional outcomes with tumor morphometry data necessitates 3D segmentation of tumors (typically based on magnetic resonance imaging). Expert delineation is the long-held gold standard for tumor segmentation, but is exceptionally resource intensive and subject to intrarater and inter-rater variability. Automated tumor segmentation algorithms have been demonstrated for a variety of imaging modalities and tumor phenotypes, but translation of these methods across clinical study designs is problematic given variation in image acquisition, tumor characteristics, segmentation objectives, and validation criteria. Herein, the authors demonstrate an alternative approach for high-throughput tumor segmentation using Internet-based, collaborative labeling.
Methods:
In a study of 85 human raters and 98 tumor patients, raters were recruited from a general university campus population (i.e., no specific medical knowledge), given minimal training, and provided web-based tools to label MRI images based on 2D cross sections. The labeling goal was characterized as to extract the enhanced tumor cores on T1-weighted MRI and the bright abnormality on T2-weighted MRI. An experienced rater manually constructed the ground truth volumes of a randomly sampled subcohort of 48 tumor subjects (for both T1w and T2w). Raters’ taskwise individual observations, as well as the volumewise truth estimates via statistical fusion method, were evaluated over the subjects having the ground truth.
Results:
Individual raters were able to reliably characterize (with >0.8 dice similarity coefficient, DSC) the gadolinium-enhancing cores and extent of the edematous areas only slightly more than half of the time. Yet, human raters were efficient in terms of providing these highly variable segmentations (less than 20 s per slice). When statistical fusion was used to combine the results of seven raters per slice for all slices in the datasets, the 3D agreement of the fused results with expertly delineated segmentations was on par with the inter-rater reliability observed between experienced raters using traditional 3D tools (approximately 0.85 DSC). The cumulative time spent per tumor patient with the collaborative approach was equivalent to that with an experienced rater, but the collaborative approach could be achieved with less training time, fewer resources, and efficient parallelization.
Conclusions:
Hence, collaborative labeling is a promising technique with potentially wide applicability to cost-effective manual labeling of medical images. Malignant gliomas represent an aggressive class of central nervous system neoplasms. Correlation of interventional outcomes with tumor morphometry data necessitates 3D segmentation of tumors (typically based on magnetic resonance imaging). Expert delineation is the long-held gold standard for tumor segmentation, but is exceptionally resource intensive and subject to intrarater and inter-rater variability. Automated tumor segmentation algorithms have been demonstrated for a variety of imaging modalities and tumor phenotypes, but translation of these methods across clinical study designs is problematic given variation in image acquisition, tumor characteristics, segmentation objectives, and validation criteria. Herein, the authors demonstrate an alternative approach for high-throughput tumor segmentation using Internet-based, collaborative labeling. In a study of 85 human raters and 98 tumor patients, raters were recruited from a general university campus population (i.e., no specific medical knowledge), given minimal training, and provided web-based tools to label MRI images based on 2D cross sections. The labeling goal was characterized as to extract the enhanced tumor cores on T1-weighted MRI and the bright abnormality on T2-weighted MRI. An experienced rater manually constructed the ground truth volumes of a randomly sampled subcohort of 48 tumor subjects (for both T1w and T2w). Raters' taskwise individual observations, as well as the volume wise truth estimates via statistical fusion method, were evaluated over the subjects having the ground truth. Individual raters were able to reliably characterize (with >0.8 dice similarity coefficient, DSC) the gadolinium-enhancing cores and extent of the edematous areas only slightly more than half of the time. Yet, human raters were efficient in terms of providing these highly variable segmentations (less than 20 s per slice). When statistical fusion was used to combine the results of seven raters per slice for all slices in the datasets, the 3D agreement of the fused results with expertly delineated segmentations was on par with the inter-rater reliability observed between experienced raters using traditional 3D tools (approximately 0.85 DSC). The cumulative time spent per tumor patient with the collaborative approach was equivalent to that with an experienced rater, but the collaborative approach could be achieved with less training time, fewer resources, and efficient parallelization. Hence, collaborative labeling is a promising technique with potentially wide applicability to cost-effective manual labeling of medical images. Malignant gliomas represent an aggressive class of central nervous system neoplasms. Correlation of interventional outcomes with tumor morphometry data necessitates 3D segmentation of tumors (typically based on magnetic resonance imaging). Expert delineation is the long-held gold standard for tumor segmentation, but is exceptionally resource intensive and subject to intrarater and inter-rater variability. Automated tumor segmentation algorithms have been demonstrated for a variety of imaging modalities and tumor phenotypes, but translation of these methods across clinical study designs is problematic given variation in image acquisition, tumor characteristics, segmentation objectives, and validation criteria. Herein, the authors demonstrate an alternative approach for high-throughput tumor segmentation using Internet-based, collaborative labeling.PURPOSEMalignant gliomas represent an aggressive class of central nervous system neoplasms. Correlation of interventional outcomes with tumor morphometry data necessitates 3D segmentation of tumors (typically based on magnetic resonance imaging). Expert delineation is the long-held gold standard for tumor segmentation, but is exceptionally resource intensive and subject to intrarater and inter-rater variability. Automated tumor segmentation algorithms have been demonstrated for a variety of imaging modalities and tumor phenotypes, but translation of these methods across clinical study designs is problematic given variation in image acquisition, tumor characteristics, segmentation objectives, and validation criteria. Herein, the authors demonstrate an alternative approach for high-throughput tumor segmentation using Internet-based, collaborative labeling.In a study of 85 human raters and 98 tumor patients, raters were recruited from a general university campus population (i.e., no specific medical knowledge), given minimal training, and provided web-based tools to label MRI images based on 2D cross sections. The labeling goal was characterized as to extract the enhanced tumor cores on T1-weighted MRI and the bright abnormality on T2-weighted MRI. An experienced rater manually constructed the ground truth volumes of a randomly sampled subcohort of 48 tumor subjects (for both T1w and T2w). Raters' taskwise individual observations, as well as the volume wise truth estimates via statistical fusion method, were evaluated over the subjects having the ground truth.METHODSIn a study of 85 human raters and 98 tumor patients, raters were recruited from a general university campus population (i.e., no specific medical knowledge), given minimal training, and provided web-based tools to label MRI images based on 2D cross sections. The labeling goal was characterized as to extract the enhanced tumor cores on T1-weighted MRI and the bright abnormality on T2-weighted MRI. An experienced rater manually constructed the ground truth volumes of a randomly sampled subcohort of 48 tumor subjects (for both T1w and T2w). Raters' taskwise individual observations, as well as the volume wise truth estimates via statistical fusion method, were evaluated over the subjects having the ground truth.Individual raters were able to reliably characterize (with >0.8 dice similarity coefficient, DSC) the gadolinium-enhancing cores and extent of the edematous areas only slightly more than half of the time. Yet, human raters were efficient in terms of providing these highly variable segmentations (less than 20 s per slice). When statistical fusion was used to combine the results of seven raters per slice for all slices in the datasets, the 3D agreement of the fused results with expertly delineated segmentations was on par with the inter-rater reliability observed between experienced raters using traditional 3D tools (approximately 0.85 DSC). The cumulative time spent per tumor patient with the collaborative approach was equivalent to that with an experienced rater, but the collaborative approach could be achieved with less training time, fewer resources, and efficient parallelization.RESULTSIndividual raters were able to reliably characterize (with >0.8 dice similarity coefficient, DSC) the gadolinium-enhancing cores and extent of the edematous areas only slightly more than half of the time. Yet, human raters were efficient in terms of providing these highly variable segmentations (less than 20 s per slice). When statistical fusion was used to combine the results of seven raters per slice for all slices in the datasets, the 3D agreement of the fused results with expertly delineated segmentations was on par with the inter-rater reliability observed between experienced raters using traditional 3D tools (approximately 0.85 DSC). The cumulative time spent per tumor patient with the collaborative approach was equivalent to that with an experienced rater, but the collaborative approach could be achieved with less training time, fewer resources, and efficient parallelization.Hence, collaborative labeling is a promising technique with potentially wide applicability to cost-effective manual labeling of medical images.CONCLUSIONSHence, collaborative labeling is a promising technique with potentially wide applicability to cost-effective manual labeling of medical images. |
Author | Chambless, Lola Landman, Bennett A. Thompson, Reid Xu, Zhoubing Asman, Andrew J. Singh, Eesha |
Author_xml | – sequence: 1 givenname: Zhoubing surname: Xu fullname: Xu, Zhoubing organization: Electrical Engineering, Vanderbilt University, Nashville, Tennessee 37235 – sequence: 2 givenname: Andrew J. surname: Asman fullname: Asman, Andrew J. organization: Electrical Engineering, Vanderbilt University, Nashville, Tennessee 37235 – sequence: 3 givenname: Eesha surname: Singh fullname: Singh, Eesha organization: Electrical Engineering, Vanderbilt University, Nashville, Tennessee 37235 – sequence: 4 givenname: Lola surname: Chambless fullname: Chambless, Lola organization: Neurosurgery, Vanderbilt University, Nashville, Tennessee 37235 – sequence: 5 givenname: Reid surname: Thompson fullname: Thompson, Reid organization: Neurosurgery, Vanderbilt University, Nashville, Tennessee 37235 – sequence: 6 givenname: Bennett A. surname: Landman fullname: Landman, Bennett A. email: bennett.landman@vanderbilt.edu organization: Electrical Engineering, Vanderbilt University, Nashville, Tennessee 37235 and Biomedical Engineering, Johns Hopkins University, Baltimore, Maryland 21218 |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/23039636$$D View this record in MEDLINE/PubMed |
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Copyright | American Association of Physicists in Medicine 2012 American Association of Physicists in Medicine Copyright © 2012 American Association of Physicists in Medicine 2012 American Association of Physicists in Medicine |
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Keywords | tumor segmentation Malignant glioma collaborative labeling statistical fusion |
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Notes | bennett.landman@vanderbilt.edu Author to whom correspondence should be addressed. Electronic mail ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 Author to whom correspondence should be addressed. Electronic mail: bennett.landman@vanderbilt.edu |
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Malignant gliomas represent an aggressive class of central nervous system neoplasms. Correlation of interventional outcomes with tumor morphometry... Malignant gliomas represent an aggressive class of central nervous system neoplasms. Correlation of interventional outcomes with tumor morphometry data... |
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SubjectTerms | Anatomy biomedical MRI Blood-Brain Barrier - metabolism Brain Cancer Central nervous system collaborative labeling Computer software Cooperative Behavior Data Interpretation, Statistical Digital computing or data processing equipment or methods, specially adapted for specific applications Edema - complications Edge enhancement gadolinium Glioma - complications Glioma - diagnosis Glioma - metabolism Graduates Humans Image data processing or generation, in general image enhancement Image enhancement or restoration, e.g. from bit‐mapped to bit‐mapped creating a similar image image fusion Image Processing, Computer-Assisted - methods image sampling image segmentation Imaging, Three-Dimensional Information integration Internet Involving electronic [emr] or nuclear [nmr] magnetic resonance, e.g. magnetic resonance imaging Magnetic Resonance Imaging Magnetic Resonance Physics Malignant glioma medical image processing Medical image segmentation Medical imaging MRI: anatomic, functional, spectral, diffusion neurophysiology Probability theory, stochastic processes, and statistics Segmentation statistical analysis statistical fusion tumor segmentation tumours |
Title | Segmentation of malignant gliomas through remote collaboration and statistical fusion |
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