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晚期前列腺癌激素治疗的最新进展

Recent progress in hormonal therapy for advanced prostate cancer.

作者信息

Daskivich Timothy J, Oh William K

机构信息

Dana-Farber Cancer Institute and Harvard Medical School, 44 Binney Street, Boston, MA 02115, USA.

出版信息

Curr Opin Urol. 2006 May;16(3):173-8. doi: 10.1097/01.mou.0000193392.77469.e2.

Abstract

PURPOSE OF REVIEW

Primary androgen deprivation therapy and secondary hormonal therapy remain the cornerstones of treatment for advanced prostate cancer. This review outlines the basic evidence for use of hormonal therapy while highlighting major research developments made in the past year.

RECENT FINDINGS

Recent research on androgen deprivation therapy has suggested that patients with high-risk features may have longer metastasis-free survival with early initiation of androgen deprivation therapy. Fracture risk has been shown to be significantly increased in patients on androgen deprivation therapy and is correlated with duration of treatment. In the treatment of androgen-independent prostate cancer, oral premarin has been shown to induce of prostate specific antigen responses more than 50% in 32% of patients, though thromboembolism remains a risk despite prophylactic low-dose warfarin. Transdermal estradiol has been associated with virtually no cardiovascular toxicity, but induced of prostate specific antigen responses more than 50% in only 12.5% of patients. Clinical studies of nilutamide, flutamide, and ketoconazole have further clarified efficacy of these secondary hormonal treatments.

SUMMARY

Optimal timing of androgen deprivation therapy awaits the results of randomized trials, but available evidence indicates that patients with high-risk features may benefit from early androgen deprivation therapy. New estrogen-based therapies have shown promising efficacy in the treatment of androgen-independent prostate cancer, with significantly less cardiovascular toxicity than traditional estrogens.

摘要

综述目的

原发性雄激素剥夺疗法和继发性激素疗法仍然是晚期前列腺癌治疗的基石。本综述概述了激素疗法使用的基本证据,同时突出了过去一年取得的主要研究进展。

最新发现

近期关于雄激素剥夺疗法的研究表明,具有高危特征的患者早期开始雄激素剥夺疗法可能有更长的无转移生存期。已证明接受雄激素剥夺疗法的患者骨折风险显著增加,且与治疗持续时间相关。在去势抵抗性前列腺癌的治疗中,已表明口服倍美力在32%的患者中可使前列腺特异性抗原反应诱导率超过50%,尽管使用低剂量预防性华法林,血栓栓塞风险仍然存在。经皮雌二醇几乎与心血管毒性无关,但仅在12.5%的患者中可使前列腺特异性抗原反应诱导率超过50%。尼鲁米特、氟他胺和酮康唑的临床研究进一步明确了这些继发性激素治疗的疗效。

总结

雄激素剥夺疗法的最佳时机有待随机试验的结果,但现有证据表明,具有高危特征的患者可能从早期雄激素剥夺疗法中获益。新型雌激素类疗法在去势抵抗性前列腺癌的治疗中显示出有前景的疗效,心血管毒性明显低于传统雌激素。

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