Geisler J, Ekse D, Hösch S, Lønning P E
Department of Oncology and Therapeutic Radiophysics, Haukeland University Hospital, Bergen, Norway.
J Steroid Biochem Mol Biol. 1995 Nov;55(2):193-5. doi: 10.1016/0960-0760(95)00163-t.
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 (E1), estradiol (E2) and estrone sulphate (E1S) 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 E2 and E1 fell slightly (mean decrease 19.4 and 16.7% respectively, n.s.). On the contrary, plasma levels of E1S increased by a mean value of 23.5% (P = 0.068). The ratio of E1S to E1 and E1S to E2 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.
屈洛昔芬(3 - 羟基他莫昔芬)是一种新型抗雌激素药物,目前正在进行治疗乳腺癌患者的临床研究。我们对一组14名每日服用40mg屈洛昔芬的绝经后女性,在基线期及治疗3个月后测定了血浆性激素结合球蛋白(SHBG)和促性腺激素(LH和FSH)水平。在8名患者的亚组中测定了血浆雌酮(E1)、雌二醇(E2)和硫酸雌酮(E1S)水平。屈洛昔芬治疗期间血浆SHBG平均升高16.6%(P < 0.05),而血浆LH和FSH水平分别平均下降15.7%(无统计学意义)和18.1%(P < 0.05)。血浆E2和E1水平略有下降(平均分别下降19.4%和16.7%,无统计学意义)。相反,血浆E1S水平平均升高23.5%(P = 0.068)。E1S与E1以及E1S与E2的比值分别平均升高48.3%(P < 0.025)和53.2%(P < 0.025)。每日40mg屈洛昔芬对血浆SHBG水平的影响与他莫昔芬治疗期间所见相似,但程度较小。与他莫昔芬相反,屈洛昔芬对血浆LH水平的抑制作用较小,提示屈洛昔芬对垂体的雌激素激动作用较小。