Gliomas are the most common primary brain tumour diagnosed in adults. Gliob
lastoma multiforme, the most aggressive grade of glioma, is the most freque
nt. Despite current treatment with a combination of surgery, radiation and
chemotherapy, median survival of patients with high-grade gliomas remains l
ess than 1 year.
Recent advances in understanding the molecular events leading to tumourigen
esis have identified new targets for current and potential therapy. The tyr
osine kinase receptors have been found to be overexpressed in most human ca
ncers, including those of the CNS. In particular, activation of the recepto
r subtypes for epidermal growth factor, platelet-derived growth factor and
vascular endothelial growth factor has been shown to lead to an increase in
cellular proliferation, angiogenesis and invasion. Agents and therapies wh
ich block the activation of these receptors have been shown to inhibit vari
ous neoplastic processes such as growth, invasion and angiogenesis, and may
in the future become a routine component of the therapeutic armamentarium.