Chowdhury Simon, Kirby Roger
The Prostate Centre, London, UK.
Practitioner. 2013 Apr;257(1760):15-8, 2.
Prostate cancer is the most common cancer in men in the UK. It accounts for nearly a quarter of all male cancer diagnoses and is the second most common cause of male cancer death. Despite a large increase in prostate cancer incidence, mortality rates have remained relatively constant through improvements in survival. Most patients present with localised disease, but there are still many who present with metastatic disease. Prostate cancers are driven by androgens, such as testosterone. Androgen deprivation therapy (ADT), which is still the mainstay of systemic treatment, effectively reduces intraprostatic androgen levels resulting in reduced androgen receptor (AR) stimulation and increased apoptosis. Medical castration using LHRH analogues has become the gold standard in managing both locally advanced prostate cancer, in ombination with radiotherapy, and metastatic disease. Eventually most men with advanced prostate cancer become resistant to ADT. This is now called castrate refractory prostate cancer (CRPC), and is associated with a poor prognosis. There is now hope for patients who progress after chemotherapy with the emergence of several new agents that have been shown to benefit patients. The first AR-targeted drug to show a definite clinical benefit is abiraterone. It markedly decreases levels of androgens in CRPC and initial trials showed promising activity. Enzalutamide has a high affinity and selectivity for AR binding, blocks nuclear translocation and reduces recruitment of co-activators. Abiraterone, enzalutamide and other AR-targeted drugs are being studied in clinical trials for patients earlier in their disease, e.g. in addition to ADT at first presentation of metastatic disease, where it is likely that greater benefits will be seen.
前列腺癌是英国男性中最常见的癌症。它占所有男性癌症诊断病例的近四分之一,是男性癌症死亡的第二大常见原因。尽管前列腺癌发病率大幅上升,但通过生存率的提高,死亡率一直保持相对稳定。大多数患者表现为局限性疾病,但仍有许多患者表现为转移性疾病。前列腺癌由雄激素驱动,如睾酮。雄激素剥夺疗法(ADT)仍是全身治疗的主要手段,它能有效降低前列腺内雄激素水平,从而减少雄激素受体(AR)的刺激并增加细胞凋亡。使用促性腺激素释放激素(LHRH)类似物进行药物去势已成为治疗局部晚期前列腺癌(联合放疗)和转移性疾病的金标准。最终,大多数晚期前列腺癌男性会对ADT产生耐药性。现在这被称为去势抵抗性前列腺癌(CRPC),且预后较差。随着几种已被证明对患者有益的新药的出现,化疗后病情进展的患者现在有了希望。首个显示出明确临床益处的AR靶向药物是阿比特龙。它能显著降低CRPC患者体内的雄激素水平,初步试验显示出有前景的活性。恩杂鲁胺对AR结合具有高亲和力和选择性,可阻断核转位并减少共激活因子的募集。阿比特龙、恩杂鲁胺和其他AR靶向药物正在针对疾病早期患者进行临床试验研究,例如在转移性疾病首次出现时除ADT外使用,可能会看到更大的益处。