Pinto Álvaro
Medical Oncology Department; University Hospital La Paz; IdiPAZ; Madrid, Spain.
Cancer Biol Ther. 2014 Feb;15(2):149-55. doi: 10.4161/cbt.26724. Epub 2013 Nov 1.
Prostate cancer is a heterogeneous disease where the previous concept of "hormone resistance" has been changed by a new generation of hormonal therapies that have proven efficacy in the castration-resistant setting. The fact is that androgens play a crucial role in the whole clinical course of prostate cancer, even when a patient meets castration-resistance criteria. The development of abiraterone showed how important and clinically meaningful can be to achieve the lowest possible levels of testosterone, and androgen receptor overexpression, mutation, or enhanced crosstalk with other pathways, which can also be targeted with new agents tested in the last few years. New androgen biosynthesis inhibitors have been developed, such as orteronel (TAK-700), but also new antiandrogens (enzalutamide, ARN-509, ODM-201) or even agents with a dual mechanism of action (galeterone). In this review the development of new hormonal therapies following the arrival of abiraterone for the treatment of prostate cancer will be summarized.
前列腺癌是一种异质性疾病,以往“激素抵抗”的概念已被新一代激素疗法所改变,这些疗法在去势抵抗性前列腺癌中已证实具有疗效。事实上,即使患者达到去势抵抗标准,雄激素在前列腺癌的整个临床过程中仍起着关键作用。阿比特龙的研发表明,将睾酮水平尽可能降低以及针对雄激素受体过表达、突变或与其他信号通路增强的串扰具有何等重要的临床意义,而过去几年所试验的新型药物也可针对这些情况。新型雄激素生物合成抑制剂已研发出来,如奥特睾酮(TAK-700),还有新型抗雄激素药物(恩杂鲁胺、ARN-509、ODM-201),甚至还有具有双重作用机制的药物(加列睾酮)。在本综述中,将总结阿比特龙问世后新型激素疗法在前列腺癌治疗方面的进展。