Gartrell Benjamin A, Saad Fred
aDepartment of Medical Oncology, Montefiore Medical Center, Albert Einstein College of Medicine, New York, USA bCentre Hospitalier de I'Université de Montréal, Hôpital Notre-Dame, Montreal, Canada.
Curr Opin Urol. 2014 Nov;24(6):595-600. doi: 10.1097/MOU.0000000000000105.
This review will describe the management of patients with prostate cancer and bone metastases with a particular emphasis on recent advances in this area.
Two osteoclast-targeted agents have been shown to decrease the incidence of skeletal-related events in patients with metastatic castration-resistant prostate cancer (mCRPC) and bone metastases. These agents are the bisphosphonate zoledronic acid and the monoclonal antibody denosumab. Recent advances in the field include the approval of several agents shown to extend survival in mCRPC. Among these agents, the androgen-pathway inhibitors, abiraterone and enzalutamide, are shown to decrease the incidence of skeletal-related events, whereas the radiopharmaceutical radium-223 is shown to reduce the incidence of symptomatic skeletal event. Cabozantinib, an agent in development, has shown encouraging activity in patients with mCRPC and bone metastases; definitive phase III trials of this agent are underway. Phase III metastasis-prevention trials are also underway in nonmetastatic CRPC.
Osteoclast-targeted agents reduce skeletal-related events in mCRPC. Disease-modifying agents also reduce the skeletal morbidity associated with mCRPC. Multiple agents are now available to reduce the skeletal morbidity of prostate cancer, whereas agents in development may provide additional options in the future.
本综述将描述前列腺癌伴骨转移患者的管理,尤其着重于该领域的近期进展。
两种靶向破骨细胞的药物已被证明可降低转移性去势抵抗性前列腺癌(mCRPC)伴骨转移患者发生骨相关事件的发生率。这些药物是双膦酸盐唑来膦酸和单克隆抗体地诺单抗。该领域的近期进展包括批准了几种可延长mCRPC患者生存期的药物。在这些药物中,雄激素途径抑制剂阿比特龙和恩杂鲁胺可降低骨相关事件的发生率,而放射性药物镭-223可降低有症状骨事件的发生率。正在研发的卡博替尼在mCRPC伴骨转移患者中已显示出令人鼓舞的活性;该药物的确定性III期试验正在进行中。非转移性CRPC的III期转移预防试验也正在进行中。
靶向破骨细胞的药物可降低mCRPC患者的骨相关事件。疾病修饰药物也可降低与mCRPC相关的骨发病率。现在有多种药物可降低前列腺癌的骨发病率,而正在研发的药物未来可能会提供更多选择。