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Meeting ReportMultimodality and Non-radioactive Molecular Imaging: Oncology Investigations

Simultaneous MR-PET of human brain tumors – Initial experience

Ciprian Catana, Thomas Benner, Elizabeth Gerstner, Dominique Jennings, Larry Byars, Michael Hamm, Christian Michel, Matthias Schmand, Bruce Rosen and Gregory Sorensen
Journal of Nuclear Medicine May 2009, 50 (supplement 2) 68;
Ciprian Catana
1AA Martinos Center for Biomedical Imaging, Radiology, MGH, Charlestown, MA
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Thomas Benner
1AA Martinos Center for Biomedical Imaging, Radiology, MGH, Charlestown, MA
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Elizabeth Gerstner
1AA Martinos Center for Biomedical Imaging, Radiology, MGH, Charlestown, MA
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Dominique Jennings
1AA Martinos Center for Biomedical Imaging, Radiology, MGH, Charlestown, MA
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Larry Byars
2Siemens Medical Solutions USA Inc, Knoxville, TN
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Michael Hamm
3Siemens Medical Solutions USA Inc, Charlestown, MA
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Christian Michel
2Siemens Medical Solutions USA Inc, Knoxville, TN
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Matthias Schmand
2Siemens Medical Solutions USA Inc, Knoxville, TN
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Bruce Rosen
1AA Martinos Center for Biomedical Imaging, Radiology, MGH, Charlestown, MA
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Gregory Sorensen
1AA Martinos Center for Biomedical Imaging, Radiology, MGH, Charlestown, MA
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Abstract

68

Objectives Demonstrate the feasibility of the prototype integrated MR-PET scanner developed by Siemens for performing simultaneous data acquisition in brain tumor patients.

Methods Subjects were injected with ~190 MBq of FDG and the distribution of the tracer was recorded at steady state. The images were reconstructed using the OP-OSEM 3D algorithm. MR data were acquired simultaneously using standard sequences (e.g. TSE, FLAIR, MPRAGE, MRA TOF and MRS). Advanced MR studies with DTI, and Gd-based DCE and DSC using EPI readout were also performed during the PET data acquisition. Ktrans, CBF, CBV, MTT maps were generated from these data.

Results No obvious artifacts caused by mutual interference were observed in the PET or the MR data. The maps obtained from the dynamic MR studies demonstrated regions with increased CBF, vascular permeability and microvascular proliferation that correlated with the region with increased glucose metabolism. However, these regions did not overlap perfectly, suggesting the distinct and complementary nature of the information provided by the two techniques in the assessment of the tumor environment.

Conclusions The simultaneous acquisition of MR and PET data is possible and, based on these preliminary studies, the two systems appear to not interfere with each other. Experiments with other PET tracers are underway. In addition to providing the anatomical context for analyzing the PET data, combining advanced functional imaging techniques could improve our understanding of the tumor microenvironment.

  • © 2009 by Society of Nuclear Medicine
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Journal of Nuclear Medicine
Vol. 50, Issue supplement 2
May 2009
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Simultaneous MR-PET of human brain tumors – Initial experience
Ciprian Catana, Thomas Benner, Elizabeth Gerstner, Dominique Jennings, Larry Byars, Michael Hamm, Christian Michel, Matthias Schmand, Bruce Rosen, Gregory Sorensen
Journal of Nuclear Medicine May 2009, 50 (supplement 2) 68;

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Simultaneous MR-PET of human brain tumors – Initial experience
Ciprian Catana, Thomas Benner, Elizabeth Gerstner, Dominique Jennings, Larry Byars, Michael Hamm, Christian Michel, Matthias Schmand, Bruce Rosen, Gregory Sorensen
Journal of Nuclear Medicine May 2009, 50 (supplement 2) 68;
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