We have shown that ICI 182780 inhibits the growth of metastatic tumour
cells derived from patients failing treatment with tamoxifen when gro
wn in vitro. In this system tamoxifen stimulates growth of tumour cell
s which can be reversed by addition of ICI 182780 to tamoxifen in cult
ure. In a phase I study we have demonstrated that treatment of patient
s for 7 days before surgical excision of the tumour resulted in marked
down regulation of ER, inhibition of growth and oestrogen-induced gen
e expression. More recently we demonstrated that treatment of advanced
breast cancer patients with ICI 182780, after tamoxifen failure, resu
lted in a high remission rate and prolonged periods of remission with
very few side-effects. These data indicate that further clinical trial
s of ICI 182780 are warranted. We expect that it will show superiority
over conventional endocrine therapy.