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激素/抗激素撤药及地塞米松用于激素难治性前列腺癌

Hormone/antihormone withdrawal and dexamethasone for hormone-refractory prostate cancer.

作者信息

Nishiyama T, Terunuma M

机构信息

Department of Urology, Koseiren Nagaoka Chuo General Hospital, Fukuzumi, Japan.

出版信息

Int J Urol. 1998 Jan;5(1):44-7. doi: 10.1111/j.1442-2042.1998.tb00233.x.

Abstract

BACKGROUND

Flutamide withdrawal has been reported to benefit patients with hormone-refractory prostate cancer. Several studies have also demonstrated that a combination of corticosteroids and testicular androgen ablation lowers serum androgen levels and improves clinical response. The purpose of this study was to examine the effect of withdrawal of oral hormonal agents and administration of dexamethasone in stage D3 prostate cancer patients.

METHODS

Sixteen patients with hormone-refractory prostate cancer were enrolled in the study. All patients had osseous metastasis and elevated serum prostate-specific antigen. Nine had been treated with chlormadinone acetate, 4 with estramustine phosphate, and 3 with flutamide as first-line hormonal therapy. All patients had also been treated either with bilateral orchiectomy (13 cases) or a luteinizing hormone-releasing hormone (LH-RH) agonist (3 cases). Seven patients whose disease progressed following hormone withdrawal were treated with oral dexamethasone (initially 1.5 mg/day, then tapered to 0.5 mg/day).

RESULTS

Eight patients demonstrated a decrease in prostate-specific antigen of greater than 50% following hormone withdrawal. The time to cancer progression for these 8 patients was 2 to 15 months (mean, 4 months). Among the patients receiving dexamethasone, 4 showed a greater than 90% decrease in prostate-specific antigen after 3 months' treatment. The time to disease progression for these 4 patients was 3 to 11 months.

CONCLUSION

In treating hormone-refractory advanced prostate cancer, the first pharmacologic manipulation should be withdrawal of the oral component of combined hormonal therapy. Patients whose disease progresses after hormone withdrawal should then be treated with glucocorticoids such as dexamethasone.

摘要

背景

据报道,氟他胺撤药对激素难治性前列腺癌患者有益。多项研究还表明,皮质类固醇与睾丸雄激素消融联合使用可降低血清雄激素水平并改善临床反应。本研究的目的是检验口服激素药物撤药及地塞米松给药对D3期前列腺癌患者的影响。

方法

16例激素难治性前列腺癌患者纳入本研究。所有患者均有骨转移且血清前列腺特异性抗原升高。9例曾接受醋酸氯地孕酮作为一线激素治疗,4例接受磷酸雌莫司汀,3例接受氟他胺。所有患者均接受了双侧睾丸切除术(13例)或促性腺激素释放激素(LH-RH)激动剂(3例)治疗。7例激素撤药后疾病进展的患者接受口服地塞米松治疗(初始剂量1.5mg/天,然后逐渐减至0.5mg/天)。

结果

8例患者激素撤药后前列腺特异性抗原下降超过50%。这8例患者的癌症进展时间为2至15个月(平均4个月)。在接受地塞米松治疗的患者中,4例在治疗3个月后前列腺特异性抗原下降超过90%。这4例患者的疾病进展时间为3至11个月。

结论

在治疗激素难治性晚期前列腺癌时,首先应进行的药物操作是撤掉联合激素治疗中的口服成分。激素撤药后疾病进展的患者随后应接受糖皮质激素如地塞米松治疗。

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