Determination of tumour hypoxia with the PET tracer [18F]EF3: improvement of the tumour-to-background ratio in a mouse tumour model.

Christian, Nicolas;Bol, Anne;De Bast, Marc;Labar, Daniel;Grégoire, Vincent;et.al.
(2007) European Journal of Nuclear Medicine and Molecular Imaging — Vol. 34, n° 9, p. 1348-1354 (2007)

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Authors
  • Christian, NicolasUCLouvain
    Author
  • Bol, AnneUCLouvain
    Author
  • De Bast, MarcUCLouvain
    Author
  • Labar, DanielUCLouvain
    Author
  • Lee, Johnorcid-logoUCLouvain
    Author
  • Mahy, PierreUCLouvain
    Author
  • Grégoire, VincentUCLouvain
    Author
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Abstract
PURPOSE: The 2-(2-nitroimidazol-1-yl)-N-(3,3,3-trifluoropropyl)acetamide (EF3) is a 2-nitroimidazole derivative which undergoes bioreductive activation under hypoxic conditions. Using the PET tracer [18F]EF3 in mice, tumour-to-muscle ratios ranging from 1.3 to 3.5 were observed. This study investigated the impact of various interventions aimed at increasing [18F]EF3 elimination, thus potentially increasing the tumour-to-noise ratio in mice, by increasing the renal filtration rate (spironolactone, furosemide), decreasing tubular re-absorption (metronidazole, ornidazole, amino acid solution) or stimulating gastro-intestinal elimination (phenobarbital). METHODS: C3H mice were injected i.v. with an average of 12.95 MBq of [18F]EF3. Drugs were injected i.v. 15 min before the tracer or daily 4 days prior to the experiment (phenobarbital). Anaesthetised mice were imaged from 30 to 300 min with a dedicated animal PET (Mosaic, Philips). Regions of interest were delineated around the tumour, bladder, heart, liver and leg muscle. Radioactivity was expressed as a percentage of injected activity per gram of tissue. RESULTS: Ornidazole decreased the urinary excretion and increased the liver uptake of [18F]EF3, but without causing any changes in the other organs. Phenobarbital significantly increased the liver concentration and decreased radioactivity in blood and muscle without affecting the tracer uptake in tumour. Consequently, a small but non-significant increase in tumour-to-noise ratio was observed. Although some effects were observed with other drugs, they did not modify the tumour-to-noise ratio. CONCLUSION: Only phenobarbital induced a trend toward an increased tumour-to-noise ratio that could possibly be tested in the clinical situation.
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Christian, N., Bol, A., De Bast, M., Labar, D., Lee, J., Mahy, P., & Grégoire, V. (2007). Determination of tumour hypoxia with the PET tracer [18F]EF3: improvement of the tumour-to-background ratio in a mouse tumour model. European Journal of Nuclear Medicine and Molecular Imaging, 34(9), 1348-1354. https://doi.org/10.1007/s00259-007-0376-7 (Original work published 2007)