Literature DB >> 9618570

Estimation of absorbed dose for 2-[F-18]fluoro-2-deoxy-D-glucose using whole-body positron emission tomography and magnetic resonance imaging.

H M Deloar1, T Fujiwara, M Shidahara, T Nakamura, H Watabe, Y Narita, M Itoh, M Miyake, S Watanuki.   

Abstract

The purpose of this study was to measure the cumulated activity and absorbed dose in organs after intravenous administration of 2-[F-18]fluoro-2-deoxy-D-glucose (18F-FDG) using whole-body positron emission tomography (PET) and magnetic resonance imaging (MRI). Whole-body dynamic emission scans for 18F-FDG were performed in six normal volunteers after transmission scans. The total activity of a source organ was obtained from the activity concentration of the organ measured by whole-body PET and the volume of that organ measured by whole-body T1-weighted MRI. The cumulated activity of each source organ was calculated from the time-activity curve. Absorbed doses to the individuals were estimated by the MIRD (medical internal radiation dosimetry) method using S-values adjusted to the individuals. Another calculation of cumulated activities and absorbed doses was performed using the organ volumes from the MIRD phantom and the "Japanese reference man" to investigate the discrepancy of actual individual results against the phantom results. The cumulated activities of 18 source organs were calculated, and absorbed doses of 27 target organs estimated. Among the target organs, bladder wall, brain and kidney received the highest doses for the above three sets of organ volumes. Using measured individual organ volumes, the average absorbed doses for those organs were found to be 3.1x10(-1), 3.7x10(-2) and 2.8x10(-2) mGy/MBq, respectively. The mean effective doses in this study for individuals of average body weight (64.5 kg) and the MIRD phantom of 70 kg were the same, i.e. 2.9x10(-2) mSv/MBq, while for the Japanese reference man of 60 kg the effective dose was 2.1x10(-2) mSv/MBq. The results for measured organ volumes derived from MRI were comparable to those obtained for organ volumes from the MIRD phantom. Although this study considered 18F-FDG, combined use of whole-body PET and MRI might be quite effective for improving the accuracy of estimations of the cumulated activity and absorbed dose of positron-labelled radiopharmaceuticals.

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Year:  1998        PMID: 9618570     DOI: 10.1007/s002590050257

Source DB:  PubMed          Journal:  Eur J Nucl Med        ISSN: 0340-6997


  32 in total

1.  An imaging co-registration system using novel non-invasive and non-radioactive external markers.

Authors:  Tung-Hsin Wu; Jiunn-Kuen Wang; Jason J S Lee; Ren-Shyan Liu; Wan-Yuo Guo
Journal:  Eur J Nucl Med Mol Imaging       Date:  2003-04-12       Impact factor: 9.236

2.  FDG-PET: procedure guidelines for tumour imaging.

Authors:  Emilio Bombardieri; Cumali Aktolun; Richard P Baum; Angelika Bishof-Delaloye; John Buscombe; Jean François Chatal; Lorenzo Maffioli; Roy Moncayo; Luc Mortelmans; Sven N Reske
Journal:  Eur J Nucl Med Mol Imaging       Date:  2003-12       Impact factor: 9.236

3.  Pittsburgh compound B (11C-PIB) and fluorodeoxyglucose (18 F-FDG) PET in patients with Alzheimer disease, mild cognitive impairment, and healthy controls.

Authors:  D P Devanand; Arthur Mikhno; Gregory H Pelton; Katrina Cuasay; Gnanavalli Pradhaban; J S Dileep Kumar; Neil Upton; Robert Lai; Roger N Gunn; V Libri; Xinhua Liu; Ronald van Heertum; J John Mann; Ramin V Parsey
Journal:  J Geriatr Psychiatry Neurol       Date:  2010-04-29       Impact factor: 2.680

4.  Is whole-body FDG-PET valuable for health screening? Against.

Authors:  Matthias Weckesser; Otmar Schober
Journal:  Eur J Nucl Med Mol Imaging       Date:  2005-03       Impact factor: 9.236

5.  Is whole-body FDG-PET valuable for health screening? For.

Authors:  Michiru Ide; Yutaka Suzuki
Journal:  Eur J Nucl Med Mol Imaging       Date:  2005-03       Impact factor: 9.236

6.  A publicly accessible Monte Carlo database for validation purposes in emission tomography.

Authors:  I Castiglioni; I Buvat; G Rizzo; M C Gilardi; J Feuardent; F Fazio
Journal:  Eur J Nucl Med Mol Imaging       Date:  2005-07-02       Impact factor: 9.236

7.  Human biodistribution and radiation dosimetry of the tachykinin NK1 antagonist radioligand [18F]SPA-RQ: comparison of thin-slice, bisected, and 2-dimensional planar image analysis.

Authors:  David R Sprague; Frederick T Chin; Jeih-San Liow; Masahiro Fujita; H Donald Burns; Richard Hargreaves; James B Stubbs; Victor W Pike; Robert B Innis; P David Mozley
Journal:  J Nucl Med       Date:  2007-01       Impact factor: 10.057

8.  Finding sensitive parameters in internal dose calculations for radiopharmaceuticals commonly used in clinical nuclear medicine.

Authors:  Vladimir Spielmann; Wei Bo Li; Maria Zankl
Journal:  Radiat Environ Biophys       Date:  2018-06-29       Impact factor: 1.925

9.  Retooling a Blood-Based Biomarker: Phase I Assessment of the High-Affinity CA19-9 Antibody HuMab-5B1 for Immuno-PET Imaging of Pancreatic Cancer.

Authors:  Jason S Lewis; Wolfgang A Weber; Christian Lohrmann; Eileen M O'Reilly; Joseph A O'Donoghue; Neeta Pandit-Taskar; Jorge A Carrasquillo; Serge K Lyashchenko; Shutian Ruan; Rebecca Teng; Wolfgang Scholz; Paul W Maffuid
Journal:  Clin Cancer Res       Date:  2019-09-20       Impact factor: 12.531

10.  Suggested pathway to assess radiation safety of ¹⁸F-labeled PET tracers for first-in-human studies.

Authors:  Paolo Zanotti-Fregonara; Adriaan A Lammertsma; Robert B Innis
Journal:  Eur J Nucl Med Mol Imaging       Date:  2013-07-19       Impact factor: 9.236

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