Molecular Imaging and Therapy Service, Memorial Sloan Kettering Cancer Center, New York, NY.
Molecular Imaging and Therapy Service, Memorial Sloan Kettering Cancer Center, New York, NY.
Semin Radiat Oncol. 2021 Jan;31(1):71-82. doi: 10.1016/j.semradonc.2020.07.004.
Theranostics in men with metastatic castration-resistant prostate cancer (mCRPC) has been developed to target bone and the tumor itself. Currently, bone-directed targeted alpha therapy with radium-223 (Ra) is the only theranostic agent proven to prolong survival in men with mCRPC who have symptomatic bone metastases and no known visceral metastases. The clinical utility and therapeutic success of Ra has encouraged the development of other tumor-targeting theranostic agents in mCRPC, primarily targeting prostate-specific membrane antigen (PSMA) with radioligand therapy (RLT). There is increasing evidence of promising response rates and a low toxicity profile with Lu-labeled PSMA RLT in patients with mCRPC. A phase III randomized study of Lu-labeled PSMA RLT has completed accrual and is awaiting results as to whether the drug improves radiographic progression-free survival and overall survival in men with mCRPC receiving standard of care treatments. Additional early clinical trials are investigating the role of tumor-directed targeted alpha therapy with radiotracers such as Ac. In this article, we review the current status of theranostics in prostate cancer, discussing the challenges and opportunities of combination therapies with more conventional agents such as androgen receptor inhibitors, cytotoxic chemotherapy, and immunotherapy.
在转移性去势抵抗性前列腺癌(mCRPC)患者中,治疗策略旨在针对骨骼和肿瘤本身。目前,镭-223(Ra)的骨靶向靶向α治疗是唯一被证明可延长有症状骨转移且无已知内脏转移的 mCRPC 男性患者生存的治疗方法。Ra 的临床应用和治疗成功鼓励了其他针对 mCRPC 的肿瘤靶向治疗方法的发展,主要是用放射性配体疗法(RLT)靶向前列腺特异性膜抗原(PSMA)。越来越多的证据表明,Lu 标记的 PSMA RLT 在 mCRPC 患者中具有较高的缓解率和较低的毒性特征。一项 Lu 标记的 PSMA RLT 的 III 期随机研究已经完成了入组,正在等待结果,以确定该药物是否能改善接受标准治疗的 mCRPC 男性的无影像学进展生存期和总生存期。其他早期临床试验正在研究放射性示踪剂如 Ac 的肿瘤靶向靶向α治疗的作用。本文综述了前列腺癌治疗方法的现状,讨论了与雄激素受体抑制剂、细胞毒性化疗和免疫疗法等更常规药物联合治疗的挑战和机遇。