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dc.date.accessioned2023-08-18T15:49:48Z
dc.date.available2023-08-18T15:49:48Z
dc.date.created2023-02-18T19:24:50Z
dc.date.issued2023
dc.identifier.citationJuzenienne, Asta Stenberg, Vilde Yuli Bruland, Øyvind Rootwelt-Revheim, Mona Elisabeth Larsen, Roy Hartvig . Dual targeting with 224Ra/212Pb-conjugates for targeted alpha therapy of disseminated cancers: A conceptual approach. Frontiers in medicine. 2023, 9
dc.identifier.urihttp://hdl.handle.net/10852/103398
dc.description.abstractMetastases are the primary cause of death among cancer patients and efficacious new treatments are sorely needed. Targeted alpha-emitting radiopharmaceuticals that are highly cytotoxic may fulfill this critical need. The focus of this paper is to describe and explore a novel technology that may improve the therapeutic effect of targeted alpha therapy by combining two radionuclides from the same decay chain in the same solution. We hypothesize that the dual targeting solution containing bone-seeking 224 Ra and cell-directed complexes of progeny 212 Pb is a promising approach to treat metastatic cancers with bone and soft tissue lesions as well as skeletal metastases of mixed lytic/osteoblastic nature. A novel liquid 224 Ra/ 212 Pb-generator for rapid preparation of a dual targeting solution is described. Cancer cell targeting monoclonal antibodies, their fragments, synthetic proteins or peptides can all be radiolabeled with 212 Pb in the 224 Ra-solution in transient equilibrium with daughter nuclides. Thus, 224 Ra targets stromal elements in sclerotic bone metastases and 212 Pb-chelated-conjugate targets tumor cells of metastatic prostate cancer or osteosarcoma. The dual targeting solution may also be explored to treat metastatic breast cancer or multiple myeloma after manipulation of bone metastases to a more osteoblastic phenotype by the use of bisphosphonates, denosumab, bortezomib or hormone therapy prior to treatment. This may improve targeting of bone-seeking 224 Ra and render an augmented radiation dose deposited within metastases. Our preliminary preclinical studies provide conceptual evidence that the dual 224 Ra-solution with bone or tumor-targeted delivery of 212 Pb has potential to inhibit cancer metastases without significant toxicity. In some settings, the use of a booster dose of purified 212 Pb-conjugate alone could be required to elevate the effect of this tumor cell directed component, if needed, e.g., in a fractionated treatment regimen, where the dual targeting solution will act as maintenance treatment.
dc.languageEN
dc.rightsAttribution 4.0 International
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.titleDual targeting with 224Ra/212Pb-conjugates for targeted alpha therapy of disseminated cancers: A conceptual approach
dc.title.alternativeENEngelskEnglishDual targeting with 224Ra/212Pb-conjugates for targeted alpha therapy of disseminated cancers: A conceptual approach
dc.typeJournal article
dc.creator.authorJuzenienne, Asta
dc.creator.authorStenberg, Vilde Yuli
dc.creator.authorBruland, Øyvind
dc.creator.authorRootwelt-Revheim, Mona Elisabeth
dc.creator.authorLarsen, Roy Hartvig
cristin.unitcode185,15,4,50
cristin.unitnameBiofysikk og medisinsk fysikk
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode1
dc.identifier.cristin2127243
dc.identifier.bibliographiccitationinfo:ofi/fmt:kev:mtx:ctx&ctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.jtitle=Frontiers in medicine&rft.volume=9&rft.spage=&rft.date=2023
dc.identifier.jtitleFrontiers in medicine
dc.identifier.volume9
dc.identifier.pagecount0
dc.identifier.doihttps://doi.org/10.3389/fmed.2022.1051825
dc.type.documentTidsskriftartikkel
dc.type.peerreviewedPeer reviewed
dc.source.issn2296-858X
dc.type.versionPublishedVersion
cristin.articleid151825


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