Abstract
Purpose
To investigate the feasibility of reducing the acquisition time for continuous dynamic positron emission tomography (PET) while retaining acceptable performance in quantifying kinetic metrics of 2-[18F]-fluoro-2-deoxy-D-glucose ([18F]FDG) in tumors.
Methods
In total, 78 oncological patients underwent total-body dynamic PET imaging for ≥ 60 min, with 8, 20, and 50 patients receiving full activity (3.7 MBq/kg), half activity (1.85 MBq/kg), and ultra-low activity (0.37 MBq/kg) of [18F]FDG, respectively. The dynamic data were divided into 21-, 30-, 45- and ≥ 60-min groups. The kinetic analysis involved model fitting to derive constant rates (VB, K1 to k3, and Ki) for both tumors and normal tissues, using both reversible and irreversible two-tissue-compartment models. One-way ANOVA with repeated measures or the Freidman test compared the kinetic metrics among groups, while the Deming regression assessed the correlation of kinetic metrics among groups.
Results
All kinetic metrics in the 30-min and 45-min groups were statistically comparable to those in the ≥ 60-min group. The relative differences between the 30-min and ≥ 60-min groups ranged from 12.3% ± 15.1% for K1 to 29.8% ± 30.0% for VB, and those between the 45-min and ≥ 60-min groups ranged from 7.5% ± 8.7% for Ki to 24.0% ± 24.3% for VB. However, this comparability was not observed between the 21-min and ≥ 60-min groups. The significance trend of these comparisons remained consistent across different models (reversible or irreversible), administrated activity levels, and partial volume corrections for lesions. Significant correlations in tumor kinetic metrics were identified between the 30-/45-min and ≥ 60-min groups, with Deming regression slopes > 0.813. In addition, the comparability of kinetic metrics between the 30-min and ≥ 60-min groups were established for normal tissues.
Conclusion
The acquisition time for dynamic PET imaging can be reduced to 30 min without compromising the ability to reveal tumor kinetic metrics of [18F]FDG, using the total-body PET/CT system.
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Data availability
The dataset used and/or analyzed in current study are available from the corresponding author on reasonable request.
Code availability
Not applicable.
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Funding
This study was funded by the Shanghai Municipal Key Clinical Specialty Project (grant number: SHSLCZDZK03401), the Major Science and Technology Projects for Major New Drug Creation (grant number: 2019ZX09302001), the Shanghai Science and Technology Committee program (grant number: 20DZ2201800), and the Three-year Action Plan of Clinical Skills and Innovation of Shanghai Hospital Development Center (grant number: SHDC2020CR3079B).
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This study was approved by the Ethics Committee of Zhongshan Hospital of Fudan University (approval number: B2019-160).
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Guobing Liu, Yimeng Shi and Xiaoguang Hou contributed equally to this article.
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Liu, G., Shi, Y., Hou, X. et al. Dynamic total-body PET/CT imaging with reduced acquisition time shows acceptable performance in quantification of [18F]FDG tumor kinetic metrics. Eur J Nucl Med Mol Imaging 51, 1371–1382 (2024). https://doi.org/10.1007/s00259-023-06526-4
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DOI: https://doi.org/10.1007/s00259-023-06526-4