间歇性雄激素抑制前列腺癌:加拿大前瞻性试验和相关观察。

Molecular urology Pub Date : 2000-01-01
N Bruchovsky, L H Klotz, M Sadar, J M Crook, D Hoffart, L Godwin, M Warkentin, M E Gleave, S L Goldenberg
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引用次数: 0

摘要

加拿大间歇性雄激素抑制前瞻性试验是1995年开始的一项原型治疗倡议,用于管理局限性前列腺癌放射治疗后生化复发的患者。一项中期分析得出了一些关于基线血清前列腺特异性抗原(PSA)、最低点血清PSA、格里森评分和停止治疗时间之间关系的观察结果。在典型的雄激素依赖性肿瘤中,血清PSA对雄激素停药的反应是双期的,但随着肿瘤的早期进展,血清PSA会出现平台期。雄激素受体的配体非依赖性激活是雄激素非依赖性启动的一种机制,在实验中可以用诱骗分子抵消,在临床中可以用非甾体抗雄激素来抵消。在一些患者中,可以通过抑制5 α -还原酶来延长停药间隔,这种效果可以通过使用抗促性腺激素降低血清睾酮来加强。血清PSA的连续测量表明,间歇性雄激素抑制产生的激素相关反应范围比以前所认识的更多样化。这包括:(1)肿瘤的反复分化和凋亡电位的恢复;(2)通过快速恢复血清睾酮抑制肿瘤生长;③血清睾酮水平过低对肿瘤生长的抑制作用。这些反应是在计划间歇性雄激素抑制的前列腺癌长期治疗时应考虑到的调节方面。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Intermittent androgen suppression for prostate cancer: Canadian Prospective Trial and related observations.

The Canadian Prospective Trial of intermittent androgen suppression was a prototype therapeutic initiative started in 1995 for the management of patients in biochemical relapse after radiation for localized prostate cancer. An interim analysis has yielded several observations on the relations between baseline serum prostate specific antigen (PSA), nadir serum PSA, Gleason score, and time off-treatment. In a typical androgen-dependent tumor, the response of serum PSA to androgen withdrawal is biphasic, but with early tumor progression, plateauing of serum PSA is observed. Ligand-independent activation of the androgen receptor, a mechanism subserving the initiation of androgen independence, can be counteracted experimentally with decoy molecules and clinically with nonsteroidal antiandrogens. In some patients, it is possible to lengthen the off-treatment interval by inhibiting the enzyme 5 alpha-reductase, an effect that can be reinforced by lowering serum testosterone with an antigonadotropin. Serial measurements of serum PSA indicate that intermittent androgen suppression engenders a more diverse range of hormone-related responses than previously appreciated. These include: (1) repeated differentiation of tumor with recovery of apoptotic potential; (2) inhibition of tumor growth by rapid restoration of serum testosterone; and (3) restraint of tumor growth by subnormal levels of serum testosterone. These responses are aspects of regulation that should be taken into account when planning long-term treatment of prostate cancer with intermittent androgen suppression.

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