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Research ArticleBasic Science Investigations

A Population-Based Gaussian Mixture Model Incorporating 18F-FDG PET and Diffusion-Weighted MRI Quantifies Tumor Tissue Classes

Mathew R. Divine, Prateek Katiyar, Ursula Kohlhofer, Leticia Quintanilla-Martinez, Bernd J. Pichler and Jonathan A. Disselhorst
Journal of Nuclear Medicine March 2016, 57 (3) 473-479; DOI: https://doi.org/10.2967/jnumed.115.163972
Mathew R. Divine
1Department of Preclinical Imaging and Radiopharmacy, Werner Siemens Imaging Center, Eberhard Karls University Tuebingen, Tuebingen, Germany
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Prateek Katiyar
1Department of Preclinical Imaging and Radiopharmacy, Werner Siemens Imaging Center, Eberhard Karls University Tuebingen, Tuebingen, Germany
2Max Planck Institute for Intelligent Systems, Tuebingen, Germany; and
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Ursula Kohlhofer
3Institute of Pathology, Eberhard Karls University Tuebingen, Tuebingen, Germany
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Leticia Quintanilla-Martinez
3Institute of Pathology, Eberhard Karls University Tuebingen, Tuebingen, Germany
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Bernd J. Pichler
1Department of Preclinical Imaging and Radiopharmacy, Werner Siemens Imaging Center, Eberhard Karls University Tuebingen, Tuebingen, Germany
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Jonathan A. Disselhorst
1Department of Preclinical Imaging and Radiopharmacy, Werner Siemens Imaging Center, Eberhard Karls University Tuebingen, Tuebingen, Germany
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Abstract

The aim of our study was to create a novel Gaussian mixture modeling (GMM) pipeline to model the complementary information derived from18F-FDG PET and diffusion-weighted MRI (DW-MRI) to separate the tumor microenvironment into relevant tissue compartments and follow the development of these compartments longitudinally. Methods: Serial 18F-FDG PET and apparent diffusion coefficient (ADC) maps derived from DW-MR images of NCI-H460 xenograft tumors were coregistered, and a population-based GMM was implemented on the complementary imaging data. The tumor microenvironment was segmented into 3 distinct regions and correlated with histology. ANCOVA was applied to gauge how well the total tumor volume was a predictor for the ADC and 18F-FDG, or if ADC was a good predictor of 18F-FDG for average values in the whole tumor or average necrotic and viable tissues. Results: The coregistered PET/MR images were in excellent agreement with histology, both visually and quantitatively, and allowed for validation of the last-time-point measurements. Strong correlations were found for the necrotic (r = 0.88) and viable fractions (r = 0.87) between histology and clustering. The GMM provided probabilities for each compartment with uncertainties expressed as a mixture of tissues in which the resolution of scans was inadequate to accurately separate tissues. The ANCOVA suggested that both ADC and 18F-FDG in the whole tumor (P = 0.0009, P = 0.02) as well as necrotic (P = 0.008, P = 0.02) and viable (P = 0.003, P = 0.01) tissues were a positive, linear function of total tumor volume. ADC proved to be a positive predictor of 18F-FDG in the whole tumor (P = 0.001) and necrotic (P = 0.02) and viable (P = 0.0001) tissues. Conclusion: The complementary information of 18F-FDG and ADC longitudinal measurements in xenograft tumors allows for segmentation into distinct tissues when using the novel GMM pipeline. Leveraging the power of multiparametric PET/MRI in this manner has the potential to take the assessment of disease outcome beyond RECIST and could provide an important impact to the field of precision medicine.

  • PET/MR
  • Gaussian mixture model
  • 18F-FDG
  • DWI

Footnotes

  • Published online Dec. 10, 2015.

  • © 2016 by the Society of Nuclear Medicine and Molecular Imaging, Inc.
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Journal of Nuclear Medicine: 57 (3)
Journal of Nuclear Medicine
Vol. 57, Issue 3
March 1, 2016
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A Population-Based Gaussian Mixture Model Incorporating 18F-FDG PET and Diffusion-Weighted MRI Quantifies Tumor Tissue Classes
Mathew R. Divine, Prateek Katiyar, Ursula Kohlhofer, Leticia Quintanilla-Martinez, Bernd J. Pichler, Jonathan A. Disselhorst
Journal of Nuclear Medicine Mar 2016, 57 (3) 473-479; DOI: 10.2967/jnumed.115.163972

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A Population-Based Gaussian Mixture Model Incorporating 18F-FDG PET and Diffusion-Weighted MRI Quantifies Tumor Tissue Classes
Mathew R. Divine, Prateek Katiyar, Ursula Kohlhofer, Leticia Quintanilla-Martinez, Bernd J. Pichler, Jonathan A. Disselhorst
Journal of Nuclear Medicine Mar 2016, 57 (3) 473-479; DOI: 10.2967/jnumed.115.163972
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Keywords

  • PET/MR
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