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[土瑞烯酮对前列腺癌患者游离、生物活性睾酮水平的抑制作用]

[Inhibition of the free, biologically active testosterone level by Turisteron in patients with prostate cancer].

作者信息

Stahl F, Schnorr D, Rohde W, Dörner G

出版信息

Z Urol Nephrol. 1987 Mar;80(3):135-8.

PMID:3604472
Abstract

Apart from their antigonadotropic effect oestrogens also directly inhibit the androgen secretion of the testicles. Thus, on the 20th day of treatment the LH-level after 12 g diethylstilbestrol diphosphate (DSDP) decreases only to approximately 50% of the initial value, while the whole testosterone (T), however, is reduced to less than 5%. The sexual hormone binding globulin is significantly more increased (p less than 0.001) by the estrogen treatment than after orchidectomy only. Therefore, the free, biologically active T-level in the plasma consists of more than one third of the level after exclusive orchidectomy. The treatment with the depot estrogen Turisteron is clarly superior to the usual treatment Oestrasid implants. Both with and without orchidectomy the free testosterone level is significantly lower than after Oestrasid implants plus orchidectomy. Therefore, this therapy can successfully be used in the treatment of the carcinoma of the prostate also without orchidectomy.

摘要

除了具有抗促性腺激素作用外,雌激素还直接抑制睾丸的雄激素分泌。因此,在治疗第20天时,给予12克二磷酸己烯雌酚(DSDP)后,促黄体生成素(LH)水平仅降至初始值的约50%,而总睾酮(T)则降至不足5%。与仅行睾丸切除术后相比,雌激素治疗使性激素结合球蛋白显著升高(p<0.001)。因此,血浆中游离的、具有生物活性的T水平超过单纯睾丸切除术后水平的三分之一。长效雌激素Turisteron治疗明显优于常用的Oestrasid植入剂治疗。无论是否行睾丸切除术,游离睾酮水平均显著低于Oestrasid植入剂加睾丸切除术后。因此,这种疗法也可成功用于治疗前列腺癌,而无需进行睾丸切除术。

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