Shore Neal, Heidenreich Axel, Saad Fred
Carolina Urologic Research Center, Myrtle Beach, SC.
Department of Urology, Uro-Oncology, Robot-assisted and Reconstructive Urological Surgery, University Hospital of Cologne, Cologne, Germany.
Urology. 2017 Nov;109:6-18. doi: 10.1016/j.urology.2017.04.062. Epub 2017 Aug 7.
Optimal sequencing strategies for approved agents in metastatic castration-resistant prostate cancer (mCRPC) are unclear. Retrospective clinical studies suggest cross-resistance between specific therapies. This review assesses treatment decisions for mCRPC. Increased use of chemohormonal therapy in castration-sensitive disease may affect subsequent treatment decisions in mCRPC. Initial abiraterone or enzalutamide treatment may result in cross-resistance for subsequent androgen receptor-targeted therapy. Clinical responses may be seen in both docetaxel- and cabazitaxel-treated patients progressing after treatment with abiraterone or enzalutamide. These observations are supported by proposed resistance mechanisms. In conclusion, small, retrospective studies suggest cross-resistance between specific therapies in mCRPC. Larger prospective studies are required.
转移性去势抵抗性前列腺癌(mCRPC)中已获批药物的最佳序贯策略尚不清楚。回顾性临床研究表明特定疗法之间存在交叉耐药性。本综述评估了mCRPC的治疗决策。在去势敏感性疾病中增加使用化学激素疗法可能会影响mCRPC后续的治疗决策。初始使用阿比特龙或恩杂鲁胺治疗可能会导致后续雄激素受体靶向治疗出现交叉耐药性。在接受阿比特龙或恩杂鲁胺治疗后进展的多西他赛和卡巴他赛治疗的患者中均可见临床反应。这些观察结果得到了所提出的耐药机制的支持。总之,小型回顾性研究表明mCRPC中特定疗法之间存在交叉耐药性。需要开展更大规模的前瞻性研究。