The purpose of this study was to evaluate the effect of
tumor size on the uptake of 18F-fluorodeoxyglucose (FDG) and
fluoroerythronitroimidazole (
FETNIM) in a murine
sarcoma model. ICR mice were xenografted with
sarcoma 180 cell line and
tumors were allowed to grow to a weight of 0.26-5.82 grams.
18F-FDG and 18F-FETNIM were injected intravenously in separate groups of mice, and after 1 hr, the
tumors were excised and radiotracer uptake was measured. In another group of mice
tumors were autoradiographically analyzed and subjected to H & E staining. In both the FDG and
FETNIM group, per-gram radiotracer uptake by a
tumor was inversely proportional to
tumor weight. 18F-FETNIM correlated more (r = -0.593, p < 0.05) than
18F-FDG (r = -0.447, p < 0.05). Autoradiographic studies revealed that FDG accumulated in viable
tumor areas, whereas
FETNIM accumulated in both viable and partially necrotic areas. In the case of 18F-FETNIM, a direct correlation between
tumor weight and the no-uptake-area to total-
tumor-area was demonstrated. We concluded that increased
tumor size is associated with decreased uptake of
18F-FDG and
FETNIM, though this depends on the type of radiotracers and distribution of
necrosis.