Feasibility of detecting hypoxia in experimental mouse tumours with F-18-fluorinated tracers and positron emission tomography - A study evaluating [F-18]fluoromisonidazole and [F-18]fluoro-2-deoxy-D-glucose
L. Bentzen et al., Feasibility of detecting hypoxia in experimental mouse tumours with F-18-fluorinated tracers and positron emission tomography - A study evaluating [F-18]fluoromisonidazole and [F-18]fluoro-2-deoxy-D-glucose, ACTA ONCOL, 39(5), 2000, pp. 629-637
The study was designed to investigate the binding of [F-18]Fluoromisonidazo
le ([F-18]FMISO) and [F-18]Fluoro-2-deoxy-D-glucose ([F-18]FDG) in a C3H mo
use mammary carcinoma. Non-anaesthetized tumour-bearing animals breathing e
ither normal air or carbogen (to reduce tumour hypoxia) were examined by PE
T after tracer injection. Tumours were identified by radioactive labelling
and methods of defining regions of interest (ROI) in the rumours were inves
tigated. Reference tissue was selected elsewhere in the mice and the ratio
between mean radioactivity in tumour and reference tissue was compared. The
results showed a correlation between the methods of identifying ROIs and a
significantly lower tumour to reference tissue ratio for carbogen-treated
mice compared with controls when using [F-18]FMISO. Only one of the methods
showed a significant difference in the tumour labelling between treatment
groups using [F-18]FDG. The study supports the contention that [F-18]FMISO
may be able to identify hypoxia in tumours, whereas a similar role for [F-1
8]FDG is more doubtful.