Title: [(18)F]EF3 is not superior to [(18)F]FMISO for PET-based hypoxia evaluation as measured in a rat rhabdomyosarcoma tumour model
Authors: Dubois, Ludwig ×
Landuyt, Willy
Cloetens, Lieselotte
Bol, Anne
Bormans, Guy
Haustermans, Karin
Labar, Daniel
Nuyts, Johan
Grégoire, Vincent
Mortelmans, Luc #
Issue Date: Feb-2009
Series Title: European Journal of Nuclear Medicine and Molecular Imaging vol:36 issue:2 pages:209-218
Abstract: PURPOSE: The aim of this investigation was to quantitatively compare the novel positron emission tomography (PET) hypoxia marker 2-(2-nitroimidazol-1-yl)-N-(3[(18)F],3,3-trifluoropropyl)acetamide ([(18)F]EF3) with the reference hypoxia tracer [(18)F]fluoromisonidazole ([(18)F]FMISO). METHODS: [(18)F]EF3 or [(18)F]FMISO was injected every 2 days into two separate groups of rats bearing syngeneic rhabdomyosarcoma tumours. In vivo PET analysis was done by drawing regions of interest on the images of selected tissues. The resulting activity data were quantified by the percentage of injected radioactivity per gram tissue (%ID/g) and tumour to blood (T/B) ratio. The spatial distribution of radioactivity was defined by autoradiography on frozen tumour sections. RESULTS: The blood clearance of [(18)F]EF3 was faster than that of [(18)F]FMISO. The clearance of both tracers was slower in tumour tissue compared with other tissues. This results in increasing T/B ratios as a function of time post tracer injection (p.i.). The maximal [(18)F]EF3 tumour uptake, compared to the maximum [(18)F]FMISO uptake, was significantly lower at 2 h p.i. but reached similar levels at 4 h p.i. The tumour uptake for both tracers was independent of the tumour volume for all investigated time points. Both tracers showed heterogeneous intra-tumoural distribution. CONCLUSIONS: [(18)F]EF3 tumour uptake reached similar levels at 4 h p.i. compared with tumour retention observed after injection of [(18)F]FMISO at 2 h p.i. Although [(18)F]EF3 is a promising non-invasive tracer, it is not superior over [(18)F]FMISO for the visualisation of tumour hypoxia. No significant differences between [(18)F]EF3 and [(18)F]FMISO were observed with regard to the intra-tumoural distribution and the extra-tumoural tissue retention.
ISSN: 1619-7070
Publication status: published
KU Leuven publication type: IT
Appears in Collections:Laboratory of Experimental Radiotherapy
Translational Research in GastroIntestinal Disorders
Radiopharmaceutical Research
Nuclear Medicine & Molecular Imaging
Laboratory of Molecular Bacteriology (Rega Institute)
× corresponding author
# (joint) last author

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