Department of Medicine, Duke University, Durham, NC, 27710, USA.
Division of Medical Oncology, Department of Medicine, Duke University, DUMC 103861, Durham, NC, 27710, USA.
J Hematol Oncol. 2020 Oct 28;13(1):144. doi: 10.1186/s13045-020-00978-z.
Metastatic castration-resistant prostate cancer (mCRPC) remains a terminal diagnosis with an aggressive disease course despite currently approved therapeutics. The recent successful development of poly ADP-ribose polymerase (PARP) inhibitors for patients with mCRPC and mutations in DNA damage repair genes has added to the treatment armamentarium and improved personalized treatments for prostate cancer. Other promising therapeutic agents currently in clinical development include the radiotherapeutic 177-lutetium-prostate-specific membrane antigen (PSMA)-617 targeting PSMA-expressing prostate cancer and combinations of immunotherapy with currently effective treatment options for prostate cancer. Herein, we have highlighted the progress in systemic treatments for mCRPC and the promising agents currently in ongoing clinical trials.
转移性去势抵抗性前列腺癌(mCRPC)尽管有目前批准的治疗方法,但仍然是一种致命的诊断,疾病进展迅速。最近,多聚 ADP-核糖聚合酶(PARP)抑制剂在 mCRPC 患者和 DNA 损伤修复基因突变患者中的成功开发,为前列腺癌的治疗提供了更多选择,并改善了个体化治疗。目前正在临床开发中的其他有前途的治疗药物包括针对表达 PSMA 的前列腺癌的放射性治疗 177 镥-前列腺特异性膜抗原(PSMA)-617 以及免疫疗法与目前有效的前列腺癌治疗方法的联合应用。本文重点介绍了 mCRPC 的系统治疗进展和目前正在进行的临床试验中很有前途的药物。