The epidermal growth factor receptor (EGFR) signalling pathway contributes
to a number of processes important to tumour progression, including cell pr
oliferation, apoptosis, angiogenesis and metastatic spread. EGFR signalling
is thought to be an important cell survival mechanism in hormone-resistant
prostate cancer. ZD1839 ('Iressa') is an orally active, selective EGFR-tyr
osine kinase inhibitor (EGFR-TKI) which blocks signal transduction pathways
implicated in promoting cancer growth. In preclinical studies, ZD1839 alon
e, and in combination with cytotoxic agents, produced reversible growth inh
ibition and growth delay in a wide range of tumour cell lines and human tum
our xenografts. Preliminary results from phase I trials in patients with ad
vanced disease suggest that ZD1839 has an acceptable tolerability profile a
nd promising clinical efficacy in patients with a variety of tumour types,
including hormone-resistant prostate cancer, where new treatment strategies
are needed.