Juzeniene Asta, Stenberg Vilde Yuli, Bruland Øyvind Sverre, Larsen Roy Hartvig
Department of Radiation Biology, Institute for Cancer Research, Norwegian Radium Hospital, Oslo University Hospital, Montebello, 0379 Oslo, Norway.
Nucligen, Ullernchausséen 64, 0379 Oslo, Norway.
Cancers (Basel). 2021 Feb 13;13(4):779. doi: 10.3390/cancers13040779.
Bone, lymph node, and visceral metastases are frequent in castrate-resistant prostate cancer patients. Since such patients have only a few months' survival benefit from standard therapies, there is an urgent need for new personalized therapies. The prostate-specific membrane antigen (PSMA) is overexpressed in prostate cancer and is a molecular target for imaging diagnostics and targeted radionuclide therapy (theragnostics). PSMA-targeted α therapies (PSMA-TAT) may deliver potent and local radiation more selectively to cancer cells than PSMA-targeted β therapies. In this review, we summarize both the recent preclinical and clinical advances made in the development of PSMA-TAT, as well as the availability of therapeutic α-emitting radionuclides, the development of small molecules and antibodies targeting PSMA. Lastly, we discuss the potentials, limitations, and future perspectives of PSMA-TAT.
骨转移、淋巴结转移和内脏转移在去势抵抗性前列腺癌患者中很常见。由于这类患者从标准治疗中仅能获得几个月的生存益处,因此迫切需要新的个性化治疗方法。前列腺特异性膜抗原(PSMA)在前列腺癌中过度表达,是成像诊断和靶向放射性核素治疗(诊疗一体化)的分子靶点。与PSMA靶向β疗法相比,PSMA靶向α疗法(PSMA-TAT)可能更有选择性地向癌细胞传递强效局部辐射。在这篇综述中,我们总结了PSMA-TAT开发方面最近的临床前和临床进展,以及治疗性α发射放射性核素的可用性、靶向PSMA的小分子和抗体的开发。最后,我们讨论了PSMA-TAT的潜力、局限性和未来前景。