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Effects of the duration of therapy with the LHRH agonist D-ser (BUT)6 Azgly10-LHRH (ICI 118-630) on the steroid hormone content and the morphology of human testicular tissue in the treatment of patients with advanced prostate cancer.

作者信息

Kuber W, Viehberger G, Zeillinger R, Spona J

机构信息

Department of Urology, Oberwart Hospital, Austria.

出版信息

Urol Res. 1991;19(1):19-24. doi: 10.1007/BF00294016.

DOI:10.1007/BF00294016
PMID:1827557
Abstract

In 20 patients with locally advanced or metastatic prostate cancer, testicular tissue obtained by bilateral subcapsular orchidectomy was examined for steroid hormone content and morphological changes. Eight patients (group I) had not received previous treatment. Twelve patients had been treated with monthly subcutaneous doses of the depot luteinizing hormone-releasing hormone (LHRH) agonist D-ser (BUT)6 Azgly10-LHRH (ICI 118-630). Six patients (group II) had been treated for less than 6 months and 6 patients (group III) for more than 6 months. The longest duration of treatment with depot LHRH was 36 months. After 2 months of treatment (group II), maximum hormone suppression was achieved and remained unchanged even if treatment was continued for 3 years. The mean serum testosterone levels were decreased in group II (means = 0.586 mg/ml) and in group III (means = 0.575 mg/ml) and were found to be in the range of castration; a statistically significant reduction in luteinizing hormone (P less than 0.000001) and follicle-stimulating hormone (P less than 0.05) was observed in the treated patient groups. The content of the steroid hormones dihydroepiandrosterone sulfate (DHEA)-S, testosterone, androstenedione, oestradiol, progesterone and 17-alpha-hydroxyprogesterone/g testicular tissue was significantly lower in patients on LHRH agonists. The differences in concentration were particularly pronounced for DHEA-S, T and A. As in the case of serum concentrations, the testicular tissues showed no differences between groups II and III. In the treated groups a significant reduction in weight was seen, depending on the duration of therapy. Similarly, the structural changes visible by the aid of light and electron microscopes increased with the duration of therapy.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

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本文引用的文献

1
Inhibition of serum androgen levels by chronic intranasal and subcutaneous administration of a potent luteinizing hormone-releasing hormone (LH-RH) agonist in adult men.成年男性长期经鼻内和皮下给予强效促黄体生成激素释放激素(LH-RH)激动剂对血清雄激素水平的抑制作用。
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2
Inhibitory effects of a single intranasal administration of [D-Ser(TBU)6, des-Gly-NH210]LHRH ethylamide, a potent LHRH agonist, on serum steroid levels in normal adult men.强效促性腺激素释放激素(LHRH)激动剂[D-丝氨酸(叔丁基)6,去甘氨酸-NH2 10]LHRH乙酰胺单次鼻内给药对正常成年男性血清类固醇水平的抑制作用。
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戈舍瑞林。其药效学和药代动力学特性以及在前列腺癌治疗中的疗效综述。
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The luteinizing hormone-releasing hormone (LHRH)-desensitized rat pituitary: luteinizing hormone responsiveness to LHRH in vitro.促黄体生成激素释放激素(LHRH)脱敏大鼠垂体:体外促黄体生成激素对LHRH的反应性
Endocrinology. 1983 Mar;112(3):793-9. doi: 10.1210/endo-112-3-793.
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Testosterone in human plasma.人血浆中的睾酮
N Engl J Med. 1965 Oct 21;273(17):902-7. doi: 10.1056/NEJM196510212731704.
6
An LH-RH analogue (Zoladex) in the management of carcinoma of the prostate: a preliminary report comparing daily subcutaneous injections with monthly depot injections.一种促黄体生成素释放激素类似物(戈舍瑞林)用于前列腺癌治疗:每日皮下注射与每月长效注射的初步比较报告
Eur J Surg Oncol. 1985 Jun;11(2):159-65.
7
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8
Treatment of advanced carcinoma of the prostate with a depot luteinizing hormone-releasing hormone analogue (ICI-118630).用长效促黄体生成素释放激素类似物(ICI - 118630)治疗晚期前列腺癌。
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Inhibitory effects on gonadotrophin secretion and gonadal function in men during chronic treatment with a potent stimulatory luteinizing hormone-releasing hormone analogue.强效促黄体生成素释放激素类似物长期治疗男性期间对促性腺激素分泌和性腺功能的抑制作用
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