Methods: To assess the potential of thymidine for imaging brain tumors
, 20 patients with untreated (n = 14) and recurrent (n = 6) supratento
rial intracranial tumors were studied with PET by using 2-[C-11]thymid
ine (Tdr), and the results were compared with [F-18]fluorodeoxyglucose
(FDG) PET data. Results: Blood analysis consistently revealed a rapid
clearance of the intact Tdr together with the appearance of CO2/HCO3-
that, with time, accounted for approximately 70% of the total blood a
ctivity. As soon as 10 min after tracer injection, brain images showed
a low and homogeneous Tdr distribution over the normal brain structur
es (cortex-to-blood ratio approximately 1). Visual and quantitative an
alysis revealed increased Tdr uptake (tumor-to-cortex ratio greater th
an or equal to 1.2) in 11 of 14 untreated tumors and in 5 of 6 recurre
nt tumors. No correlation was found between Tdr uptake and tumor grade
. In 12 of the 14 untreated tumors, FDG uptake was low (tumor-to-corte
x ratio: 0.83 +/- 0.79), but a FDG hot spot was visualized in 8 of 10
high-grade and in none of the 4 low-grade tumors. FDG uptake was consi
stently low in recurrent tumors (tumor-to-cortex ratio: 0.49 +/- 0.19)
, and PET-FDG was negative in 3 of the 6 cases. Conclusion: These data
indicate the feasibility of brain tumor imaging with Tdr and suggest
the potential clinical usefulness of the method in the detection of tu
mor recurrences. The specificity of the method remains, however, to be
investigated.