Phase I study of the oral nonsteroidal aromatase inhibitor CGS 20267 in healthy postmenopausal women.

We have performed a phase I study of the effect of a single dose of CGS 20267, an oral nonsteroidal aromatase inhibitor, in 12 healthy volunteer postmenopausal women. Each subject received 2 single doses of CGS 20267 (0.1, 0.5, or 2.5 mg) or placebo separated by a washout period of at least 6 weeks. There was statistically significant suppression of serum estrone and estradiol at all three doses of CGS 20267 tested. Serum estrone and estradiol concentrations were maximally suppressed by 76% and 79% from baseline levels, respectively. Urinary excretion of estrone and estradiol was also suppressed, although this did not reach statistical significance. Serum concentrations of aldosterone, cortisol, 17 alpha-hydroxyprogesterone, androstenedione, testosterone, FSH, LH, and TSH were unaffected by CGS 20267. The drug was well tolerated, with no significant side-effects. This study has shown CGS 20267 to be a potent and specific aromatase inhibitor, and further studies are now needed to assess its clinical efficacy.

[1]  A. Bhatnagar,et al.  Open dose-finding study of a new potent and selective nonsteroidal aromatase inhibitor, CGS 20 267, in healthy male subjects. , 1993, The Journal of clinical endocrinology and metabolism.

[2]  M. Dowsett,et al.  Phase I study of the oral nonsteroidal aromatase inhibitor CGS 20267 in postmenopausal patients with advanced breast cancer. , 1993, Cancer research.

[3]  J. Ménard,et al.  The effects of fadrozole hydrochloride on aldosterone secretion in healthy male subjects. , 1992, The Journal of clinical endocrinology and metabolism.

[4]  J. Raats,et al.  A study of fadrozole, a new aromatase inhibitor, in postmenopausal women with advanced metastatic breast cancer. , 1992, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

[5]  P. Lønning,et al.  Endocrine, pharmacokinetic and clinical studies of the aromatase inhibitor 3-ethyl-3-(4-pyridyl)piperidine-2,6-dione ('pyridoglutethimide') in postmenopausal breast cancer patients. , 1991, British Journal of Cancer.

[6]  M. Lang,et al.  Highly selective inhibition of estrogen biosynthesis by CGS 20267, a new non-steroidal aromatase inhibitor , 1990, The Journal of Steroid Biochemistry and Molecular Biology.

[7]  M. Dowsett,et al.  A dose-comparative endocrine-clinical study of leuprorelin in premenopausal breast cancer patients. , 1990, British Journal of Cancer.

[8]  M. Dowsett,et al.  The clinical and endocrine effects of 4-hydroxyandrostenedione alone and in combination with goserelin in premenopausal women with advanced breast cancer. , 1990, British Journal of Cancer.

[9]  M. Dowsett,et al.  POTENCY AND SELECTIVITY OF THE NON‐STEROIDAL AROMATASE INHIBITOR CGS 16949A IN POSTMENOPAUSAL BREAST CANCER PATIENTS , 1990, Clinical endocrinology.

[10]  R. Santen,et al.  The effects of CGS 16949A, an aromatase inhibitor on adrenal mineralocorticoid biosynthesis. , 1990, The Journal of clinical endocrinology and metabolism.

[11]  M. Dowsett,et al.  Preliminary study of the treatment of advanced breast cancer in postmenopausal women with the aromatase inhibitor CGS 16949A. , 1990, Cancer research.

[12]  A. Bhatnagar,et al.  A comparison of methods measuring aromatase activity in human placenta and rat ovary. , 1990, Journal of enzyme inhibition.

[13]  M. Dowsett,et al.  Dose-related endocrine effects of pharmacokinetics of oral and intramuscular 4-hydroxyandrostenedione in postmenopausal breast cancer patients : Cancer Res.; 49/5 (1306–1312)/1989/ , 1989 .

[14]  M. Dowsett,et al.  Dose-related endocrine effects and pharmacokinetics of oral and intramuscular 4-hydroxyandrostenedione in postmenopausal breast cancer patients. , 1989, Cancer research.

[15]  H. Adlercreutz,et al.  Inhibition of aromatase with CGS 16949A in postmenopausal women. , 1989, The Journal of clinical endocrinology and metabolism.

[16]  T. Powles,et al.  Use of the aromatase inhibitor 4-hydroxyandrostenedione in postmenopausal breast cancer: optimization of therapeutic dose and route. , 1987, Cancer research.

[17]  T. Powles,et al.  Treatment of advanced postmenopausal breast cancer with an aromatase inhibitor, 4-hydroxyandrostenedione: phase II report. , 1986, Cancer research.

[18]  M. Dowsett,et al.  A comparison of the endocrine effects of low dose aminoglutethimide with and without hydrocortisone in postmenopausal breast cancer patients. , 1985, British Journal of Cancer.

[19]  M. Dowsett,et al.  ENDOCRINE EFFECTS OF LOW DOSE AMINOGLUTETHIMIDE AS AN AROMATASE INHIBITOR IN THE TREATMENT OF BREAST CANCER , 1985, Clinical endocrinology.

[20]  M. Dowsett,et al.  4-HYDROXYANDROSTENEDIONE IN TREATMENT OF POSTMENOPAUSAL PATIENTS WITH ADVANCED BREAST CANCER , 1984, The Lancet.

[21]  R. Paridaens,et al.  EFFECTS OF AMINOGLUTETHIMIDE ON ADRENAL STEROID SECRETION , 1983, Clinical endocrinology.

[22]  M. Dowsett,et al.  Endocrine effects of low dose aminoglutethimide alone in advanced postmenopausal breast cancer. , 1983, British Journal of Cancer.

[23]  A. Harris,et al.  Tamoxifen versus aminoglutethimide in advanced breast carcinoma: a randomized cross-over trial. , 1981, British medical journal.

[24]  R. Santen,et al.  A randomized trial comparing surgical adrenalectomy with aminoglutethimide plus hydrocortisone in women with advanced breast cancer. , 1981, The New England journal of medicine.

[25]  R. Santen,et al.  Aminoglutethimide inhibits extraglandular estrogen production in postmenopausal women with breast carcinoma. , 1978, The Journal of clinical endocrinology and metabolism.

[26]  R. Santen,et al.  Compensatory increase in TSH secretion without effect on prolactin secretion in patients treated with aminoglutethimide. , 1977, The Journal of clinical endocrinology and metabolism.