Department of Nuclear Medicine, Klinikum Westfalen, Dortmund, Germany; Department of Nuclear Medicine, Institute of Radiology, Neuroradiology and Nuclear Medicine, University Hospital Knappschaftskrankenhaus, Bochum, Germany.
Department of Nuclear Medicine, Inselspital, Bern University Hospital, University of Bern, Bern, Switzerland.
Semin Nucl Med. 2024 Jul;54(4):581-590. doi: 10.1053/j.semnuclmed.2024.02.007. Epub 2024 Apr 4.
This review paper highlights the transformative role of PSMA-targeted diagnostics and therapy in prostate cancer management, particularly focusing on Lu-PSMA-617, approved by the FDA and EMA for metastatic castration-resistant prostate cancer (mCRPC) patients post-chemotherapy and ARPI treatment. Originating from the VISION trial's success, this paper navigates the current radioligand therapy (RLT) indications, emphasizing practical patient selection, planning, and treatment execution. It critically examines Lu-PSMA's comparative effectiveness against cabazitaxel and Ra-223, addressing decision-making dilemmas for mCRPC treatments. Furthermore, the paper discusses Lu-PSMA in chemotherapy-naïve patients and its application in hormone-sensitive prostate cancer, underlined by ongoing global studies. A significant concern is Lu-PSMA's long-term safety profile, particularly nephrotoxicity risks, necessitating further investigation. The possibility of Lu-PSMA rechallenge in responsive patients is explored, stressing the need for comprehensive analyses and real-world data to refine treatment protocols. Conclusively, PSMA-targeted therapy marks a significant advance in prostate cancer therapy, advocating for its integration into a multimodal, patient-centric treatment approach. The review underscores the imperative for additional comparative studies to optimize treatment sequences and outcomes, ultimately enhancing long-term prognosis and disease control in prostate cancer management.
这篇综述文章强调了 PSMA 靶向诊断和治疗在前列腺癌管理中的变革作用,特别是重点关注 Lu-PSMA-617,该药物已获得 FDA 和 EMA 的批准,用于化疗和 ARPI 治疗后转移性去势抵抗性前列腺癌(mCRPC)患者。它源于 VISION 试验的成功,本文探讨了当前放射性配体治疗(RLT)的适应证,强调了实际的患者选择、计划和治疗执行。它还批判性地比较了 Lu-PSMA 与 cabazitaxel 和 Ra-223 的疗效,解决了 mCRPC 治疗中的决策难题。此外,本文还讨论了 Lu-PSMA 在化疗初治患者中的应用及其在激素敏感性前列腺癌中的应用,这是由正在进行的全球研究支持的。一个值得关注的问题是 Lu-PSMA 的长期安全性概况,特别是肾毒性风险,需要进一步研究。还探讨了 Lu-PSMA 在有反应的患者中的再挑战可能性,强调需要进行全面分析和真实世界数据研究,以完善治疗方案。总之,PSMA 靶向治疗标志着前列腺癌治疗的重大进展,提倡将其纳入多模式、以患者为中心的治疗方法。该综述强调了进行额外的比较研究以优化治疗顺序和结果的必要性,最终改善前列腺癌管理中的长期预后和疾病控制。