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前列腺癌的激素治疗。

Hormonal therapy of prostate cancer.

机构信息

Research Center in Molecular Endocrinology, Oncology and Human Genomics, Laval University and Laval University Hospital Research Center (CRCHUL), Quebec, Canada.

出版信息

Prog Brain Res. 2010;182:321-41. doi: 10.1016/S0079-6123(10)82014-X.

Abstract

Of all cancers, prostate cancer is the most sensitive to hormones: it is thus very important to take advantage of this unique property and to always use optimal androgen blockade when hormone therapy is the appropriate treatment. A fundamental observation is that the serum testosterone concentration only reflects the amount of testosterone of testicular origin which is released in the blood from which it reaches all tissues. Recent data show, however, that an approximately equal amount of testosterone is made from dehydroepiandrosterone (DHEA) directly in the peripheral tissues, including the prostate, and does not appear in the blood. Consequently, after castration, the 95-97% fall in serum testosterone does not reflect the 40-50% testosterone (testo) and dihydrotestosterone (DHT) made locally in the prostate from DHEA of adrenal origin. In fact, while elimination of testicular androgens by castration alone has never been shown to prolong life in metastatic prostate cancer, combination of castration (surgical or medical with a gonadotropin-releasing hormone (GnRH) agonist) with a pure anti-androgen has been the first treatment shown to prolong life. Most importantly, when applied at the localized stage, the same combined androgen blockade (CAB) can provide long-term control or cure of the disease in more than 90% of cases. Obviously, since prostate cancer usually grows and metastasizes without signs or symptoms, screening with prostate-specific antigen (PSA) is absolutely needed to diagnose prostate cancer at an 'early' stage before metastasis occurs and the cancer becomes non-curable. While the role of androgens was believed to have become non-significant in cancer progressing under any form of androgen blockade, recent data have shown increased expression of the androgen receptor (AR) in treatment-resistant disease with a benefit of further androgen blockade. Since the available anti-androgens have low affinity for AR and cannot block androgen action completely, especially in the presence of increased AR levels, it becomes important to discover more potent and purely antagonistic blockers of AR. The data obtained with compounds under development are promising. While waiting for this (these) new anti-androgen(s), combined treatment with castration and a pure anti-androgen (bicalutamide, flutamide or nilutamide) is the only available and the best scientifically based means of treating prostate cancer by hormone therapy at any stage of the disease with the optimal chance of success and even cure in localized disease.

摘要

在所有癌症中,前列腺癌对激素最为敏感:因此,充分利用这一独特特性,在激素治疗为适当治疗时始终采用最佳雄激素阻断疗法非常重要。一个基本的观察结果是,血清睾酮浓度仅反映从睾丸释放到血液中的睾酮量,而血液中的睾酮可以到达所有组织。然而,最近的数据表明,大约等量的睾酮是由去氢表雄酮(DHEA)在包括前列腺在内的外周组织中直接产生的,而不会出现在血液中。因此,去势后,血清睾酮下降 95-97%并不能反映源自肾上腺的 DHEA 在前列腺内产生的 40-50%的睾酮(testo)和二氢睾酮(DHT)。事实上,虽然单独去势消除睾丸雄激素从未被证明可以延长转移性前列腺癌患者的生命,但去势(手术或药物去势联合促性腺激素释放激素(GnRH)激动剂)联合使用纯抗雄激素已被证明是第一种可延长生命的治疗方法。最重要的是,当应用于局限性阶段时,相同的联合雄激素阻断(CAB)可以在超过 90%的病例中提供疾病的长期控制或治愈。显然,由于前列腺癌通常在没有任何迹象或症状的情况下生长和转移,因此绝对需要进行前列腺特异性抗原(PSA)筛查,以便在转移发生之前且癌症变得无法治愈的情况下早期诊断前列腺癌。虽然在任何形式的雄激素阻断下,癌症进展过程中的雄激素作用被认为已变得不重要,但最近的数据表明,在治疗抵抗性疾病中雄激素受体(AR)的表达增加,进一步的雄激素阻断具有获益。由于现有的抗雄激素对 AR 的亲和力较低,并且不能完全阻断雄激素作用,尤其是在 AR 水平增加的情况下,发现更有效且纯粹的 AR 拮抗剂变得很重要。正在开发的化合物获得的数据很有希望。在等待这些新的抗雄激素出现的同时,去势联合使用纯抗雄激素(比卡鲁胺、氟他胺或尼鲁米特)是治疗任何阶段前列腺癌的唯一可行且基于最佳科学的激素治疗方法,在局限性疾病中具有最佳的成功甚至治愈机会。

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