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血清睪酮水平在接受 LH 释放激素治疗的前列腺癌患者中的变化:一个未解决的问题。

Variations of serum testosterone levels in prostate cancer patients under LH-releasing hormone therapy: an open question.

机构信息

Department of Surgery (Urology), Faculty of Medical Sciences, University of Campinas (Unicamp), Rua Tessália Vieira de Camargo, 126 Cidade Universitária Zeferino Vaz, Campinas, São Paulo CEP 13083-887, Brazil.

出版信息

Endocr Relat Cancer. 2012 May 24;19(3):R93-8. doi: 10.1530/ERC-12-0040. Print 2012 Jun.

Abstract

The hypothesis 'the lower the better when achieving castration levels of testosterone' is based on the data from second-line hormonal manipulation and its molecular basis, and on better oncological results reported for lower castration levels in prostate cancer (PCa) patients, including those achieved with maximal androgen blockade. In this regard, the equivalence of surgical and different pharmacological castrations has been controversial. The modified amino acid structure that makes LH-releasing hormone (LHRH) analogs more potent than LHRH, and the method of delivering the analogs impacts on bioavailibility and potentially causes differences in androgen levels and in its final oncological efficacy. In addition to this, there is a myriad of circumstances, such as those related to ethnic variations and co-morbidities, which uniquely impact on the pharmacological approach in a highly heterogeneous population of castration-resistant prostate cancer (CRPC) patients. Ineffective testosterone suppression through hormonal escape is currently poorly recognized and may result in increased PCa mortality. Until now, the optimal serum testosterone level in patients under castration, and the impact of its variations in patients under LHRH therapy, remain open questions and have been merged to a broad spectra of patients who are highly heterogeneous. This heterogeneity relates to a number of mechanisms regarding response to treatment, which influences the biology of the relapsing tumor and the sensitivity to subsequent therapies in the individual patient. The rationale to achieve testosterone levels below 20-50 ng/dl warrant further investigation as these levels have recently rescued CRPC patients. In the last few years and months, important advancements in prostate cancer treatment have been achieved. Nevertheless, these advances are measured in a few months of additional survival and under high costs, not available to most of the world population, compared with the benefits of hormonal manipulation that are measured in years, there is a huge potential for accessible and durable effect expansion and optimization of treatment, particularly with the current tendency of a more individual approach.

摘要

“实现去势水平的睾酮时越低越好”这一假说基于二线激素治疗的数据及其分子基础,以及更低的去势水平在前列腺癌(PCa)患者中所报告的更好的肿瘤学结果,包括那些通过最大雄激素阻断实现的结果。在这方面,手术去势和不同的药物去势的等效性一直存在争议。改变使黄体生成素释放激素(LHRH)类似物比 LHRH 更有效的氨基酸结构,以及类似物的给药方式都会影响生物利用度,并可能导致雄激素水平及其最终肿瘤学疗效的差异。除此之外,还有无数的情况,例如与种族差异和合并症相关的情况,这些情况会对高度异质的去势抵抗性前列腺癌(CRPC)患者的药物治疗方法产生独特的影响。目前,由于激素逃逸导致的睾酮抑制无效的情况尚未得到充分认识,可能会导致 PCa 死亡率增加。到目前为止,在接受去势治疗的患者中最佳的血清睾酮水平,以及在接受 LHRH 治疗的患者中其变化的影响,仍然是悬而未决的问题,并已合并到广泛的患者群体中,这些患者具有高度的异质性。这种异质性涉及到一系列与治疗反应相关的机制,这些机制影响复发肿瘤的生物学特性以及个体患者对后续治疗的敏感性。将睾酮水平降至 20-50ng/dl 以下的理由需要进一步研究,因为这些水平最近挽救了 CRPC 患者。在过去的几年和几个月里,前列腺癌治疗取得了重要进展。然而,与激素治疗所带来的数年获益相比,这些进展仅以几个月的额外生存时间和高昂的成本来衡量,而不是世界上大多数人都能享受到的。因此,具有巨大的潜力来扩大和优化治疗的可及性和持久性,特别是考虑到当前更倾向于个体化治疗的趋势。

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