Alpha therapies : where and when is the future in neuroendocrine tumours?

dc.contributor.authorVorster, Mariza
dc.contributor.authorGrana, Chiara Maria
dc.contributor.authorTravascio, Laura
dc.contributor.authorSathekge, Mike Machaba
dc.contributor.emailmike.sathekge@up.ac.za
dc.date.accessioned2025-11-21T06:57:13Z
dc.date.available2025-11-21T06:57:13Z
dc.date.issued2025-08
dc.descriptionDATA AVAILABILITY : No datasets were generated or analysed during the current study.
dc.description.abstractNeuroendocrine tumors (NETs) represent a diverse group of neoplasms arising from neuroendocrine cells, treatable with various modalities including targeted radionuclide therapy. Traditional treatments such as surgery, somatostatin analogues, chemotherapy, target therapies and peptide receptor radionuclide therapy (PRRT) with beta-emitting isotopes like 177Lu-DOTATATE have shown good clinical efficacy. However, 177Lu-DOTATATE may be less effective in refractory or progressive cases, necessitating the transition to alpha-emitting therapies. The emergence of alpha therapies, leveraging the potent cytotoxicity of alpha-emitting isotopes, signifies a notable advancement in the therapeutic landscape for NETs. This review aims to provide an overview of the most significant developments and evidence for the use of targeted alpha therapies in neuroendocrine tumors. Alpha particles, with their high linear energy transfer (LET) and short range, offer distinct advantages over beta particles. Their potent cytotoxicity can cause double-strand DNA breaks, leading to higher tumor cell kill rates. Several alpha-emitting isotopes, including Actinium-225, Bismuth-213, and Lead-212, are currently being investigated for their therapeutic potential in NETs. These isotopes deliver lethal radiation doses to tumor cells while minimizing collateral damage to healthy tissues, even more targeted in hepatic disease when intraarterial administration is feasible. Despite challenges related to Ac-225 production, availability, costs, dosimetry, standardization, and sufficient long-term follow-up data, the clinical success in treating resistant and aggressive forms of NETs underscores the need for increased investment and research to optimize production and distribution processes. Developing reliable supply chains and comprehending the potential long-term effects of alpha emitters are essential steps. The time for Targeted Alpha Therapies is undeniably here and now, with continued advancements holding the potential to revolutionize the treatment of neuroendocrine tumors, providing hope and improved outcomes for patients globally.
dc.description.departmentNuclear Medicine
dc.description.librarianhj2025
dc.description.sdgSDG-03: Good health and well-being
dc.description.sponsorshipOpen access funding provided by University of Pretoria.
dc.description.urihttps://link.springer.com/journal/40336
dc.identifier.citationVorster, M., Grana, C.M., Travascio, L. et al. Alpha therapies: where and when is the future in neuroendocrine tumours?. Clinical and Translational Imaging 13, 329–337 (2025). https://doi.org/10.1007/s40336-025-00692-1.
dc.identifier.issn2281-5872 (print)
dc.identifier.issn2281-7565 (online)
dc.identifier.other10.1007/s40336-025-00692-1
dc.identifier.urihttp://hdl.handle.net/2263/105427
dc.language.isoen
dc.publisherSpringer
dc.rights© The Author(s) 2025. Open Access. This article is licensed under a Creative Commons Attribution 4.0 International License.
dc.subjectNeuroendocrine tumors (NETs)
dc.subjectPeptide receptor radionuclide therapy (PRRT)
dc.subjectTAT
dc.subjectTheranostics
dc.subjectTargeted radionuclide therapies
dc.subjectAc-225
dc.subjectPb-212
dc.titleAlpha therapies : where and when is the future in neuroendocrine tumours?
dc.typeArticle

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