Positron emission, tomography (PET) assesses the uptake and distribution of
a radiopharmaceutics labelling tissue metabolism, in tumour and in presuma
bly healthy brain, respectively. This technique provides data which are com
plementary from those obtained with anatomical imaging (CT-scanner, MRI) an
d with histology performed on a biopsy sample. The most frequently used tra
cers, in neuro-oncology, are 18FDG and 11C-methionine. However, for most of
the applications of this technique, the latter tracer appears to be more e
ffective than the former, both from the point of view of sensitivity and sp
ecificity. The main applications of PET in clinical neuro-oncology are the
following:
1) when establishing the, early diagnosis of a glioma, in order to differen
tiate between cell lines (astrocytoma or oligodendroglioma) and grading;
2) during the follow-up of the tumour, in order to identify progression fro
m a low grade towards an anaplastic lesion;
3) after surgical removal, to exhibit some residual tumour,
4) after radiation therapy or chemotherapy, for an early assessment of the
response to therapy,
5) long after treatment, to differentiate between radiation necrosis and tu
mour recurrence.