INFLUENCE OF DROLOXIFENE (3-HYDROXYTAMOXIFEN), 40 MG DAILY, ON PLASMA GONADOTROPINS, SEX-HORMONE BINDING GLOBULIN AND ESTROGEN-LEVELS IN POSTMENOPAUSAL BREAST-CANCER PATIENTS

被引:13
作者
GEISLER, J
EKSE, D
HOSCH, S
LONNING, PE
机构
[1] HAUKELAND UNIV HOSP,DEPT ONCOL & THERAPEUT RADIOPHYS,N-5021 BERGEN,NORWAY
[2] KLINGE PHARMA GMBH,DEPT PHARMACOL & TOXICOL,MUNICH,GERMANY
关键词
D O I
10.1016/0960-0760(95)00163-T
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Droloxifene (3-hydroxytamoxifen) is a novel antiestrogen currently undergoing clinical investigations for treatment of breast cancer patients. We measured plasma levels of sex hormone binding globulin (SHBG) and the gonadotrophins (LH and FSH) at baseline and after 3 months on treatment in a group of fourteen postmenopausal women treated with droloxifene 40 mg daily. Plasma levels of estrone (E(1)), estradiol (E(2)) and estrone sulphate (E(1)S) were measured in a subgroup of eight patients. Plasma SHBG increased during treatment with droloxifene by a mean value of 16.6% (P < 0.05), while plasma levels of LH and FSH decreased by a mean value of 15.7% (n.s.) and 18.1% (P < 0.05), respectively. Plasma levels of E(2) and E(1) fell slightly (mean decrease 19.4 and 16.7% respectively, n.s.). On the contrary, plasma levels of E(1)S increased by a mean value of 23.5% (P = 0.068). The ratio of E(1)S to E(1) and E(1)S to E(2) increased by a mean value of 48.3% (P < 0.025) and 53.2% (P < 0.025), respectively. The effect of droloxifene 40 mg daily on plasma levels of SHBG resembles what is seen during treatment with tamoxifen but occurs to a smaller extent. Contrary to tamoxifen, droloxifene caused a minor suppression of plasma LH levels, suggesting droloxifene to have less estrogen agonistic effects on the pituitary.
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页码:193 / 195
页数:3
相关论文
共 12 条
[2]  
DOWSETT M, 1987, CANCER RES, V47, P1957
[3]  
EBCTC Group, 1992, LANCET, V339, P1
[4]   INFLUENCE OF TREATMENT WITH THE ANTIESTROGEN 3-HYDROXYTAMOXIFEN (DROLOXIFENE) ON PLASMA SEX-HORMONE LEVELS IN POSTMENOPAUSAL PATIENTS WITH BREAST-CANCER [J].
GEISLER, J ;
HAARSTAD, H ;
GUNDERSEN, S ;
RAABE, N ;
KVINNSLAND, S ;
LONNING, PE .
JOURNAL OF ENDOCRINOLOGY, 1995, 146 (02) :359-363
[5]   PRECLINICAL DATA FOR DROLOXIFENE [J].
HASMANN, M ;
RATTEL, B ;
LOSER, R .
CANCER LETTERS, 1994, 84 (02) :101-116
[6]   ENDOCRINE PHARMACOLOGY OF ANTIESTROGENS AS ANTITUMOR AGENTS [J].
JORDAN, VC ;
MURPHY, CS .
ENDOCRINE REVIEWS, 1990, 11 (04) :578-610
[7]   RELATIONS BETWEEN SEX-HORMONES, SEX-HORMONE BINDING GLOBULIN, INSULIN-LIKE GROWTH FACTOR-L AND INSULIN-LIKE GROWTH-FACTOR BINDING PROTEIN-1 IN POSTMENOPAUSAL BREAST-CANCER PATIENTS [J].
LONNING, PE ;
HELLE, SI ;
JOHANNESSEN, DC ;
ADLERCREUTZ, H ;
LIEN, EA ;
TALLY, M ;
EKSE, D ;
FOTSIS, T ;
ANKER, GB ;
HALL, K .
CLINICAL ENDOCRINOLOGY, 1995, 42 (01) :23-30
[8]   INFLUENCE OF TAMOXIFEN ON SEX-HORMONES, GONADOTROPINS AND SEX-HORMONE BINDING GLOBULIN IN POSTMENOPAUSAL BREAST-CANCER PATIENTS [J].
LONNING, PE ;
JOHANNESSEN, DC ;
LIEN, EA ;
EKSE, D ;
FOTSIS, T ;
ADLERCREUTZ, H .
JOURNAL OF STEROID BIOCHEMISTRY AND MOLECULAR BIOLOGY, 1995, 52 (05) :491-496
[9]   INVIVO AND INVITRO ANTIESTROGENIC ACTION OF 3-HYDROXYTAMOXIFEN, TAMOXIFEN AND 4-HYDROXYTAMOXIFEN [J].
LOSER, R ;
SEIBEL, K ;
ROOS, W ;
EPPENBERGER, U .
EUROPEAN JOURNAL OF CANCER & CLINICAL ONCOLOGY, 1985, 21 (08) :985-990
[10]   A MECHANISTIC HYPOTHESIS FOR DNA ADDUCT FORMATION BY TAMOXIFEN FOLLOWING HEPATIC OXIDATIVE-METABOLISM [J].
POTTER, GA ;
MCCAGUE, R ;
JARMAN, M .
CARCINOGENESIS, 1994, 15 (03) :439-442