Literature DB >> 7999408

Sex hormone levels in postmenopausal women with advanced metastatic breast cancer treated with CGS 169 49A.

B Svenstrup1, J Herrstedt, N Brünner, P Bennett, H Wachmann, P Dombernowsky.   

Abstract

30 postmenopausal patients with metastatic breast cancer were treated with three different doses of fadrozole hydrochloride (CGS 169 49A), a non-steroidal competitive aromatase inhibitor. The effect of 0.5, 1 and 2 mg given twice daily upon the levels of oestrogens, their androgen precursors and upon the concentration of sex hormone binding globulin (SHBG) was investigated after 1 and 3 months and then every 3 months until progression of disease. A significant reduction in the serum concentration of oestrone (P < 0.0001) was obtained at all doses. Also, the serum concentration of oestrone sulphate was significantly reduced (P < 0.0001). However, after 1 month, the concentration was significantly different from pretreatment levels (P < 0.01) only at the 4 mg daily dose. A decline was also observed in the concentration of SHBG (P < 0.05), with a concomitant elevation of the percentage non-SHBG-bound oestradiol. The androgens, testosterone and dehydroepiandrosterone sulphate, were unaltered during treatment, while androstendione was significantly elevated at the 2 mg daily dose (P < 0.001).

Entities:  

Mesh:

Substances:

Year:  1994        PMID: 7999408     DOI: 10.1016/0959-8049(94)90168-6

Source DB:  PubMed          Journal:  Eur J Cancer        ISSN: 0959-8049            Impact factor:   9.162


  2 in total

Review 1.  Indirect androgen doping by oestrogen blockade in sports.

Authors:  D J Handelsman
Journal:  Br J Pharmacol       Date:  2008-04-21       Impact factor: 8.739

Review 2.  Aromatase inhibitors for treatment of advanced breast cancer in postmenopausal women.

Authors:  Lorna Gibson; David Lawrence; Claire Dawson; Judith Bliss
Journal:  Cochrane Database Syst Rev       Date:  2009-10-07
  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.