Department of Oncology, Akershus University Hospital, Sykehusveien 25, 1478 Lørenskog, Norway.
Department of Oncology, Oslo University Hospital-Norwegian Radium Hospital, Ullernchausseen 70, 0379 Oslo, Norway.
Future Oncol. 2018 Oct;14(24):2543-2556. doi: 10.2217/fon-2018-0087. Epub 2018 Jun 21.
Since most patients with metastatic castration-resistant prostate cancer (mCRPC) have bone metastases, it is important to understand the potential impact of therapies on prognostic biomarkers, such as ALP. Clinical studies involving mCRPC life-prolonging agents (i.e., sipuleucel-T, abiraterone, enzalutamide, docetaxel, cabazitaxel, and radium-223) have shown that baseline ALP level is prognostic for overall survival, and may be a better prognostic marker for overall survival than prostate-specific antigen in patients with bone-dominant mCRPC. Mechanism of action differences between therapies may partly explain ALP dynamics during treatment. ALP changes can be interpreted within the context of other parameters while monitoring disease activity to better understand the underlying pathology. This review evaluates the current role of ALP in mCRPC.
由于大多数转移性去势抵抗性前列腺癌(mCRPC)患者有骨转移,因此了解治疗方法对预后生物标志物(如 ALP)的潜在影响非常重要。涉及 mCRPC 延寿药物(即 sipuleucel-T、阿比特龙、恩扎鲁胺、多西他赛、卡巴他赛和镭-223)的临床研究表明,基线 ALP 水平对总生存期具有预后意义,并且在骨优势型 mCRPC 患者中,它可能比前列腺特异性抗原更能预测总生存期。治疗方法之间的作用机制差异可能部分解释了治疗过程中 ALP 的动态变化。在监测疾病活动的同时,根据其他参数解读 ALP 的变化,以更好地了解潜在的病理。本综述评估了 ALP 在 mCRPC 中的当前作用。