作者: Mohamed Bishr , Fred Saad
关键词:
摘要: Over the past few years, we have developed an increased understanding of molecular mechanisms that underlie prostate cancer progression and castration resistance expanded our repertoire therapeutic options for castration-resistant (CRPC). Four new agents (cabazitaxel, abiraterone acetate, enzalutamide, radium-233) been shown to prolong overall survival in patients with CRPC postchemotherapy setting. Targeting androgen receptor pathway continues important role treatment CRPC, acetate enzalutamide being most exciting developments. Cabazitaxel is now considered standard-of-care second-line chemotherapy men metastatic (mCRPC). Bone-targeted therapy active area research, denosumab first bone-targeted agent able significantly delay appearance bone metastases radium-223 radiopharmaceutical improve mCRPC.