Khandwala H M, Vassilopoulou-Sellin R, Logethetis C J, Friend K E
Section of Endocrine Neoplasia and Hormonal Disorders, University of Texas, M. D. Anderson Cancer Center, Houston 77030, USA.
Endocr Pract. 2001 Jan-Feb;7(1):11-5. doi: 10.4158/EP.7.1.11.
To determine the effect of administration of corticosteroids on adrenal androgen production and the serologic markers of prostate cancer.
Six patients with prostate cancer who had a serum testosterone concentration that exceeded 20 ng/dL despite treatment with medical or surgical castration were treated with dexamethasone. All patients were asymptomatic, but four were demonstrating progressive increases in serum prostate-specific antigen (PSA) concentrations. Dexamethasone, 1 mg at bedtime, was given initially and then increased to 1 mg twice daily if serum testosterone concentrations remained > or =10 ng/dL. The effect of treatment on PSA concentration was monitored.
The mean testosterone concentration (and standard error of the mean) was 47.5 +/- 7.9 ng/dL before administration of dexamethasone; this decreased to 5.2 +/- 3.0 ng/dL during therapy (P = 0.002). The effect was rapid (overnight) and sustainable (for 6 months). Although the duration of follow-up is limited, PSA concentrations generally stabilized (23.5 +/- 6.1 ng/mL at baseline in comparison with 15.6 +/- 1.1 ng/mL approximately 2 months after initiation of dexamethasone therapy; P = 0.24). Two patients required 1 mg of dexamethasone twice daily to suppress serum testosterone levels to <10 ng/dL.
Administration of corticosteroids in a manner opposing the normal circadian glucocorticoid production effectively and rapidly decreases adrenal androgen production in patients with prostate cancer treated with orchiectomy or luteinizing hormone-releasing hormone agonists. This reduction of androgen production was generally associated with a decrease or stabilization of PSA concentrations in all patients with increased PSA levels. Overnight dexamethasone suppression testing is useful in determining the minimal effective dose.
确定给予皮质类固醇对肾上腺雄激素生成及前列腺癌血清学标志物的影响。
6例前列腺癌患者,尽管接受了药物或手术去势治疗,但血清睾酮浓度仍超过20 ng/dL,给予地塞米松治疗。所有患者均无症状,但4例患者血清前列腺特异性抗原(PSA)浓度呈进行性升高。初始给予地塞米松,睡前1 mg,若血清睾酮浓度仍≥10 ng/dL,则增至每日2次,每次1 mg。监测治疗对PSA浓度的影响。
给予地塞米松前,平均睾酮浓度(及平均标准误)为47.5±7.9 ng/dL;治疗期间降至5.2±3.0 ng/dL(P = 0.002)。效果迅速(一夜之间)且可持续(达6个月)。尽管随访时间有限,但PSA浓度总体稳定(基线时为23.5±6.1 ng/mL,地塞米松治疗开始约2个月后为15.6±1.1 ng/mL;P = 0.24)。2例患者需要每日2次给予1 mg地塞米松才能将血清睾酮水平抑制至<10 ng/dL。
以与正常昼夜糖皮质激素生成相反的方式给予皮质类固醇,可有效且迅速降低接受睾丸切除术或促性腺激素释放激素激动剂治疗的前列腺癌患者的肾上腺雄激素生成。雄激素生成的这种降低通常与所有PSA水平升高患者的PSA浓度降低或稳定有关。夜间地塞米松抑制试验有助于确定最小有效剂量。