Radiation Medicine Centre (BARC), Tata Memorial Hospital Annexe, Mumbai, India.
Radiation Medicine Centre (BARC), Homi Bhabha National Institute, Mumbai, India.
Expert Rev Anticancer Ther. 2023 Jul-Dec;23(9):959-975. doi: 10.1080/14737140.2023.2247562. Epub 2023 Aug 28.
The prostate-specific membrane antigen (PSMA) targeted radioligand therapy (PRLT) for the treatment of metastatic castration-resistant prostate cancer (mCRPC) patients has generated significant interest among the oncologic community, with several publications documenting good response rates and survival benefits with low toxicity profiles.
Indications, patient preparation, dose administration, post-treatment imaging, dosimetry, and side effect profiles of Lu-PSMA-617 are discussed in this article. We also discuss results from prospective studies, major retrospective studies, meta-analyses, clinical trials, and mentioned major ongoing clinical trials on PRLT. We have also portrayed our own experiences and future perspectives on PRLT.
For PRLT, PSMA-617 and PSMA-I&T molecules have revolutionized the theranostic approach in the management of advanced prostate cancer, with solid backing from several published articles showing favorable outcomes and an excellent safety profile of Lu-PSMA-617. Improvement in quality of life and survival was seen in the majority of mCRPC patients after Lu-PSMA-617 PRLT. Patients with good performance status, asymptomatic, only lymph node metastases, high PSMA expressing lesions, and no discordant FDG avid lesions have a longer survival after 177Lu-PSMA-617 PRLT than patients with poor performance status, symptomatic, hepatic, brain, and skeletal metastases, discordant PSMA, and FDG-avid lesions. Docetaxel and cabazitaxel are approved treatments for mCRPC patients. Lu-PSMA-617 is approved as a third-line systemic treatment for mCRPC patients with failure to respond to androgen receptor pathway inhibitors and docetaxel therapy. PRLT is a safe and effective alternative to cabazitaxel (third-line systemic treatment), but it has a higher cost. Lu-PSMA-617 could be a more efficient therapeutic option for mCRPC patients as first-line or combined therapy, and it may be a useful therapeutic option for the treatment of metastatic hormone-sensitive prostate cancer (mHSPC) patients. Several clinical studies and clinical trials on PRLT are currently underway. In the future, the results of these trials will be helpful in evolving treatment strategies for prostate cancer patients.
针对转移性去势抵抗性前列腺癌(mCRPC)患者的前列腺特异性膜抗原(PSMA)靶向放射性配体治疗(PRLT)引起了肿瘤学界的极大兴趣,多项研究记录了其具有良好的缓解率和生存获益,且毒性谱较低。
本文讨论了 Lu-PSMA-617 的适应证、患者准备、剂量管理、治疗后影像学、剂量学和副作用特征。我们还讨论了来自前瞻性研究、主要回顾性研究、荟萃分析、临床试验的结果,并提到了正在进行的关于 PRLT 的主要临床试验。我们还描绘了我们自己在 PRLT 方面的经验和未来展望。
对于 PRLT,PSMA-617 和 PSMA-I&T 分子彻底改变了晚期前列腺癌的治疗方法,有多项发表的文章为 Lu-PSMA-617 的良好结果和出色安全性提供了坚实的支持。大多数 mCRPC 患者在接受 Lu-PSMA-617 PRLT 后,生活质量和生存均得到改善。在 Lu-PSMA-617 PRLT 后,具有良好表现状态、无症状、仅有淋巴结转移、高 PSMA 表达病变、无不一致的 FDG 摄取病变的患者的生存时间较长,而表现状态差、有症状、肝、脑和骨转移、不一致的 PSMA 和 FDG 摄取病变的患者的生存时间较短。多西他赛和卡巴他赛是 mCRPC 患者的批准治疗药物。Lu-PSMA-617 被批准作为雄激素受体通路抑制剂和多西他赛治疗失败的 mCRPC 患者的三线系统治疗药物。与卡巴他赛(三线系统治疗)相比,PRLT 是一种安全有效的替代方案,但成本更高。Lu-PSMA-617 可能是 mCRPC 患者一线或联合治疗的更有效治疗选择,也可能是治疗转移性激素敏感性前列腺癌(mHSPC)患者的有用治疗选择。目前正在进行多项关于 PRLT 的临床研究和临床试验。未来,这些试验的结果将有助于为前列腺癌患者制定治疗策略。