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抗雌激素药物3-羟基他莫昔芬(屈洛昔芬)治疗对绝经后乳腺癌患者血浆性激素水平的影响。

Influence of treatment with the anti-oestrogen 3-hydroxytamoxifen (droloxifene) on plasma sex hormone levels in postmenopausal patients with breast cancer.

作者信息

Geisler J, Haarstad H, Gundersen S, Raabe N, Kvinnsland S, Lønning P E

机构信息

Department of Oncology, Haukeland University Hospital, Bergen, Norway.

出版信息

J Endocrinol. 1995 Aug;146(2):359-63. doi: 10.1677/joe.0.1460359.

Abstract

Plasma levels of oestradiol (Oe2), oestrone (Oe1) oestrone sulphate (Oe1S), androstenedione, testosterone, dehydroepiandrosterone (DHEA), dehydroepiandrosterone sulphate (DHEAS), sex hormone-binding globulin (SHBG) and the gonadotrophins (FSH and LH) were determined in 20 postmenopausal women with breast cancer treated with the anti-oestrogen droloxifene (3-hydroxytamoxifen). Plasma oestrogens were measured before and after 3, 6 and 12 months of therapy. The other hormones were measured before and after 6 months of therapy. Droloxifene treatment had no significant influence on plasma levels of Oe2. Plasma levels of Oe1 and Oe1S increased during treatment (mean increase of 11.9-15.9% and 24.5-69.4% respectively after different time-intervals on treatment). The Oe1S/Oe1 and Oe1S/Oe2 ratios increased by mean values of 13.8-45.2% and 25.9-52.4% respectively. Plasma SHBG increased significantly by a mean value of 73.9%, while FSH and LH fell non-significantly by 19.7% and 20.4% respectively. Plasma levels of testosterone, androstenedione, DHEA and DHEAS all increased during treatment, but none of these alterations were of statistical significance. While the influence of droloxifene on plasma SHBG resembled that which is seen during treatment with tamoxifen, its influence on plasma oestrogens and the gonadotrophins seems to be different. Possible explanations of such differences and the clinical implications of alterations in plasma hormones during treatment with droloxifene are discussed.

摘要

对20名接受抗雌激素药物屈洛昔芬(3-羟基他莫昔芬)治疗的绝经后乳腺癌妇女测定了血浆雌二醇(Oe2)、雌酮(Oe1)、硫酸雌酮(Oe1S)、雄烯二酮、睾酮、脱氢表雄酮(DHEA)、硫酸脱氢表雄酮(DHEAS)、性激素结合球蛋白(SHBG)以及促性腺激素(FSH和LH)的水平。在治疗3个月、6个月和12个月之前及之后测定血浆雌激素水平。在治疗6个月之前及之后测定其他激素水平。屈洛昔芬治疗对血浆Oe2水平无显著影响。治疗期间血浆Oe1和Oe1S水平升高(治疗不同时间间隔后平均分别升高11.9 - 15.9%和24.5 - 69.4%)。Oe1S/Oe1和Oe1S/Oe2比值平均分别升高13.8 - 45.2%和25.9 - 52.4%。血浆SHBG显著升高,平均值为73.9%,而FSH和LH分别非显著下降19.7%和20.4%。治疗期间血浆睾酮、雄烯二酮、DHEA和DHEAS水平均升高,但这些变化均无统计学意义。虽然屈洛昔芬对血浆SHBG的影响与他莫昔芬治疗期间所见相似,但其对血浆雌激素和促性腺激素的影响似乎不同。讨论了这些差异的可能解释以及屈洛昔芬治疗期间血浆激素变化的临床意义。

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