Summary Five men with advanced breast cancer were treated with aminoglutethimide (AG) plus replacement dose hydrocortisone. None of the 4 patients with intact testes responded, although 3 did so subsequently to tamoxifen. The previously orchidetomised patient responded to amminoglutethimide for 14 months. Oestrone and oestradiol were suppressed by AG in all patients, but not to the levels achieved by orchidectomy. AG produced substantial further oestrogen suppression in the orchidectomised patient and should only be used after orchidectomy.Breast cancer in males is an uncommon disease. It accounts for 1 % of all breast cancers and is frequently sensitive to hormone manipulation (Ribeiro, 1985). Breast cancer in men presents at a more advanced stage and in older age groups compared with women, but when matched for these prognostic variables, survival is similar (Scheike, 1982). Because of these clinical features, systemic endocrine therapy is commonly combined with local treatment, castration being a standard first line endocrine approach.Recently, aminoglutethimide has been shown to be effective in postmenopausal women with breast cancer, the main mechanism of action being inhibition of the peripheral conversion of androgens to oestrogens by aromatase (Harris et al., 1982a;1983a). In men, three quarters of oestradiol produced results from peripheral aromatisation of testosterone (Epstein et al., 1966;Longcope et al., 1969;Wu et al., 1982). Thus aminoglutethimide could potentially be useful either to avoid castration or as a second line endocrine therapy to suppress residual oestrogen production via androgens from the adrenal after castration.
Patients and methodsFive men with advanced breast cancer were treated with aminoglutethimide and replacement dose hydrocortisone (20mg twice daily). Four patients received the conventional dose of aminoglutethimide, 250 mg four times daily, and one received 125mg twice daily.Plasma samples were taken before treatment and at 2 weekly intervals for measurement of oestrone, Correspondence: A.L. Harris.