Honest Ndlovu, Ismaheel O Lawal, Joseph Kabunda, Chimbabantu Kaoma, Khomotso Mashigoane, Zane Knoesen, Kamo Ramonaheng, Sandile Sibiya, Amanda Mdlophane, Sipho Mdanda, Thomas Ebenhan, Mankgopo Kgatle, JanRijn Zeevaart, Kgomotso M Mokoala, Akram Al-Ibraheem, Mike Sathekge
{"title":"Targeted alpha therapy in prostate cancer: review of available agents in clinical practice.","authors":"Honest Ndlovu, Ismaheel O Lawal, Joseph Kabunda, Chimbabantu Kaoma, Khomotso Mashigoane, Zane Knoesen, Kamo Ramonaheng, Sandile Sibiya, Amanda Mdlophane, Sipho Mdanda, Thomas Ebenhan, Mankgopo Kgatle, JanRijn Zeevaart, Kgomotso M Mokoala, Akram Al-Ibraheem, Mike Sathekge","doi":"10.23736/S1824-4785.25.03642-8","DOIUrl":null,"url":null,"abstract":"<p><p>Targeted alpha therapy (TAT) has shown promise in prostate cancer patients, both hormone-sensitive and castration-resistant, with or without prior treatment. TAT's radiobiological properties explain why it is more potent than other forms of ionizing radiation, such as the clinically approved [<sup>177</sup>Lu]Lu-PSMA-617. Although most TAT agents used in compassionate care or clinical trials target the prostate-specific membrane antigen (PSMA), some alternatives are yet to be used clinically, some of which aim to address PSMA-negative prostate cancer. These include [<sup>223</sup>Ra]RaCl2, which is approved for palliative bone pain, and a variety of other non-PSMA antigen or receptor-targeting medicines. Whereas this study focuses on TAT medicines that are currently available for clinical use, it also explores these preclinical agents.</p>","PeriodicalId":49135,"journal":{"name":"the Quarterly Journal of Nuclear Medicine and Molecular Imaging","volume":"69 2","pages":"118-128"},"PeriodicalIF":1.4000,"publicationDate":"2025-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"the Quarterly Journal of Nuclear Medicine and Molecular Imaging","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.23736/S1824-4785.25.03642-8","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Targeted alpha therapy (TAT) has shown promise in prostate cancer patients, both hormone-sensitive and castration-resistant, with or without prior treatment. TAT's radiobiological properties explain why it is more potent than other forms of ionizing radiation, such as the clinically approved [177Lu]Lu-PSMA-617. Although most TAT agents used in compassionate care or clinical trials target the prostate-specific membrane antigen (PSMA), some alternatives are yet to be used clinically, some of which aim to address PSMA-negative prostate cancer. These include [223Ra]RaCl2, which is approved for palliative bone pain, and a variety of other non-PSMA antigen or receptor-targeting medicines. Whereas this study focuses on TAT medicines that are currently available for clinical use, it also explores these preclinical agents.
期刊介绍:
The Quarterly Journal of Nuclear Medicine and Molecular Imaging publishes scientific papers on clinical and experimental topics of nuclear medicine. Manuscripts may be submitted in the form of editorials, original articles, review articles and special articles. The journal aims to provide its readers with papers of the highest quality and impact through a process of careful peer review and editorial work.