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在接受去势治疗的前列腺癌患者中,使用抗雄激素药物治疗后,基础状态及促肾上腺皮质激素刺激状态下肾上腺雄激素的血浆水平受到抑制。

Inhibition of basal and adrenocorticotropin-stimulated plasma levels of adrenal androgens after treatment with an antiandrogen in castrated patients with prostatic cancer.

作者信息

Bélanger A, Dupont A, Labrie F

出版信息

J Clin Endocrinol Metab. 1984 Sep;59(3):422-6. doi: 10.1210/jcem-59-3-422.

Abstract

The basal plasma levels of cortisol, dehydroepiandrosterone (DHEA), DHEA sulfate (DHEA-S), and testosterone were studied in 20 patients with advanced prostatic cancer receiving combined treatment with an LHRH agonist and an antiandrogen [5,5-dimethyl-3-[4-nitro-3-(trifluoromethyl)-phenyl]-2 4-imidazolidinedione]. After 60 days of combined antihormonal therapy, plasma levels of testosterone decreased from 5.44 +/- 0.44 (SEM) to 0.136 +/- 0.052 ng/ml (2.5% of control). Somewhat unexpectedly, the plasma concentrations of the adrenal androgens DHEA and DHEA-S were reduced to 45 +/- 7 and 64 +/- 4% of control, respectively. The maximal reduction in plasma adrenal androgen levels occurred between 2 and 4 weeks of treatment. Whereas the increase in serum cortisol, 17-hydroxypregnenolone, and 17-hydroxyprogesterone concentrations 2 1/2 h after the injection of 0.25 mg human ACTH 1-24 was not affected by the combined treatment, the increment of DHEA and androstenedione after the same stimulus was reduced from 3.1 +/- 0.98 and 0.73 +/- 0.11 to 1.48 +/- 0.5 and 0.31 +/- 0.05 ng/ml, respectively. The reduced levels of serum DHEA and DHEA-S were not due to the LHRH agonist by itself, since similarly low levels of serum DHEA and DHEA-S were found in patients surgically castrated and receiving the same antiandrogen. These data suggest that treatment with an antiandrogen in castrated men inhibit the formation of adrenal androgens due to a blockade at the level of 17, 20-desmolase. The efficiency of the new combined antihormonal therapy (castration and antiandrogen) aimed at complete androgen neutralization in prostate cancer is thus further facilitated.

摘要

对20例晚期前列腺癌患者进行了研究,这些患者接受促性腺激素释放激素(LHRH)激动剂和抗雄激素药物[5,5-二甲基-3-[4-硝基-3-(三氟甲基)-苯基]-2,4-咪唑烷二酮]联合治疗,测定了他们皮质醇、脱氢表雄酮(DHEA)、硫酸脱氢表雄酮(DHEA-S)和睾酮的基础血浆水平。联合抗激素治疗60天后,睾酮血浆水平从5.44±0.44(标准误)降至0.136±0.052 ng/ml(为对照值的2.5%)。有点出乎意料的是,肾上腺雄激素DHEA和DHEA-S的血浆浓度分别降至对照值的45±7%和64±4%。血浆肾上腺雄激素水平的最大降幅出现在治疗的2至4周之间。注射0.25 mg人促肾上腺皮质激素1-24后2.5小时,血清皮质醇、17-羟孕烯醇酮和17-羟孕酮浓度的升高不受联合治疗的影响,但相同刺激后DHEA和雄烯二酮的增量分别从3.1±0.98和0.73±0.11降至1.48±0.5和0.31±0.05 ng/ml。血清DHEA和DHEA-S水平降低并非由于LHRH激动剂本身,因为在接受手术去势并服用相同抗雄激素药物的患者中也发现了类似低水平的血清DHEA和DHEA-S。这些数据表明,去势男性使用抗雄激素治疗可抑制肾上腺雄激素的形成,原因是在17,20-碳链裂解酶水平存在阻断。因此,旨在完全中和前列腺癌雄激素的新联合抗激素治疗(去势和抗雄激素)效率得到进一步提高。

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