Ling Sui Wai, de Blois Erik, Hooijman Eline, van der Veldt Astrid, Brabander Tessa
Department of Radiology & Nuclear Medicine, Erasmus MC, 3015 GD Rotterdam, The Netherlands.
Department of Hospital Pharmacy, Erasmus MC, 3015 GD Rotterdam, The Netherlands.
Pharmaceutics. 2022 Oct 11;14(10):2166. doi: 10.3390/pharmaceutics14102166.
For patients with metastatic castration-resistant prostate cancer (mCRPC), the survival benefit of classic treatment options with chemotherapy and drugs targeting androgen signaling is limited. Therefore, beta and alpha radionuclide therapy (RNT) have emerged as novel treatment options for patients with mCRPC. Radioligands target the prostate-specific membrane antigen (PSMA) epitopes, which are upregulated up to a thousand times more in prostate cancer cells compared to the cells in normal tissues. For this reason, PSMA is an excellent target for both imaging and therapy. Over the past years, many studies have investigated the treatment effects of lutetium-177 labeled PSMA (Lu-PSMA) and actinium-225 labeled PSMA (Ac-PSMA) RNT in patients with mCRPC. While promising results have been achieved, this field is still in development. In this review, we have summarized and discussed the clinical data of Lu-PSMA and Ac-PSMA RNT in patients with mCRPC.
对于转移性去势抵抗性前列腺癌(mCRPC)患者,经典的化疗和靶向雄激素信号通路药物治疗方案的生存获益有限。因此,β和α放射性核素治疗(RNT)已成为mCRPC患者的新型治疗选择。放射性配体靶向前列腺特异性膜抗原(PSMA)表位,与正常组织细胞相比,PSMA在前列腺癌细胞中的上调幅度高达千倍之多。因此,PSMA是成像和治疗的理想靶点。在过去几年中,许多研究调查了镥-177标记的PSMA(Lu-PSMA)和锕-225标记的PSMA(Ac-PSMA)RNT对mCRPC患者的治疗效果。虽然已取得了令人鼓舞的结果,但该领域仍在发展中。在本综述中,我们总结并讨论了Lu-PSMA和Ac-PSMA RNT治疗mCRPC患者的临床数据。