Our goal was to determine whether PET with C-11-methionine and/or (18)
FDG could predict malignancy grade in non-Hodgkin's lymphoma (NHL). Me
thods: Twenty-three patients with high-grade, low-grade or transformed
low-grade NHL were investigated. Standardized uptake values (SUV), tr
ansport rate and mass influx values were calculated both for the whole
tumor [mean regions of interest, (ROI)] and for the tumor area with t
he highest levels of activity, comprising four contiguous pixels withi
n each tumor and designated as a hot spot. Results: Both C-11-methioni
ne and (18)FDG detected all tumors. In addition, (18)FDG discriminated
between high- and low-grade NHL, whereas C-11-methionine did not. Wit
h (18)FDG, three transformed low-grade NHLs behaved in an intermediate
manner. All quantitative uptake values correlated well with each othe
r for both tracers, except for the mean ROI SUV and transport rate of
C-11-methionine. Quantifications of mean ROI uptake and hot spots were
strongly correlated. Conclusion: The results of this study together w
ith previous findings from other studies indicate that (18)FDG but not
C-11-methionine can predict malignancy grade in NHL. Further studies
with a larger series of patients are needed.