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Radionuclide Therapy of Unresectable Tumors with AvidinOX and (90)Y-biotinDOTA: Tongue Cancer Paradigm

Local treatment of unresectable tumors is challenging, particularly with radioactivity. Current practice relies on external beam irradiation or on a variety of medical devices for brachytherapy. Both approaches proved useful in controlling tumor growth, but are characterized by poor compliance of th...

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Autores principales: Albertoni, Claudio, Leoni, Barbara, Rosi, Antonio, D'Alessio, Valeria, Carollo, Valeria, Spagnoli, Luigi Giusto, van Echteld, Cees, De Santis, Rita
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Mary Ann Liebert, Inc. 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4575534/
https://www.ncbi.nlm.nih.gov/pubmed/26167947
http://dx.doi.org/10.1089/cbr.2015.1837
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author Albertoni, Claudio
Leoni, Barbara
Rosi, Antonio
D'Alessio, Valeria
Carollo, Valeria
Spagnoli, Luigi Giusto
van Echteld, Cees
De Santis, Rita
author_facet Albertoni, Claudio
Leoni, Barbara
Rosi, Antonio
D'Alessio, Valeria
Carollo, Valeria
Spagnoli, Luigi Giusto
van Echteld, Cees
De Santis, Rita
author_sort Albertoni, Claudio
collection PubMed
description Local treatment of unresectable tumors is challenging, particularly with radioactivity. Current practice relies on external beam irradiation or on a variety of medical devices for brachytherapy. Both approaches proved useful in controlling tumor growth, but are characterized by poor compliance of the patient, significant side-effects, high costs, and technological complexity, which hamper widespread use. The authors recently described a novel form of radionuclide therapy based on the oxidized form of avidin that, chemically reacting with tissue proteins, can secure radioactive biotin within the injected tissue, either when precomplexed or when taken from the blood stream after intravenous administration. AvidinOX-pretargeted (177)Lu-biotinDOTA ((177)Lu-ST2210) is currently under clinical investigation for the treatment of liver oligometastases from colorectal cancer (clinicaltrials.gov/NCT02053324). In the present work, the authors show that injected AvidinOX can link tissues of various natures such as prostate, kidney, breast, or brain and can react by contact with scraped tissues such as skin or urinary bladder. AvidinOX injected into human OSC19 tongue cancer masses orthotopically transplanted in nude mice takes up intravenously administered (90)Y-ST2210, which exerts significant antitumor activity, while preserving the integrity and functionality of the tongue. Present data confirm that AvidinOX-based radionuclide therapy is an innovative and promising approach for the local treatment of inoperable tumors.
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spelling pubmed-45755342015-09-29 Radionuclide Therapy of Unresectable Tumors with AvidinOX and (90)Y-biotinDOTA: Tongue Cancer Paradigm Albertoni, Claudio Leoni, Barbara Rosi, Antonio D'Alessio, Valeria Carollo, Valeria Spagnoli, Luigi Giusto van Echteld, Cees De Santis, Rita Cancer Biother Radiopharm Original Articles Local treatment of unresectable tumors is challenging, particularly with radioactivity. Current practice relies on external beam irradiation or on a variety of medical devices for brachytherapy. Both approaches proved useful in controlling tumor growth, but are characterized by poor compliance of the patient, significant side-effects, high costs, and technological complexity, which hamper widespread use. The authors recently described a novel form of radionuclide therapy based on the oxidized form of avidin that, chemically reacting with tissue proteins, can secure radioactive biotin within the injected tissue, either when precomplexed or when taken from the blood stream after intravenous administration. AvidinOX-pretargeted (177)Lu-biotinDOTA ((177)Lu-ST2210) is currently under clinical investigation for the treatment of liver oligometastases from colorectal cancer (clinicaltrials.gov/NCT02053324). In the present work, the authors show that injected AvidinOX can link tissues of various natures such as prostate, kidney, breast, or brain and can react by contact with scraped tissues such as skin or urinary bladder. AvidinOX injected into human OSC19 tongue cancer masses orthotopically transplanted in nude mice takes up intravenously administered (90)Y-ST2210, which exerts significant antitumor activity, while preserving the integrity and functionality of the tongue. Present data confirm that AvidinOX-based radionuclide therapy is an innovative and promising approach for the local treatment of inoperable tumors. Mary Ann Liebert, Inc. 2015-09-01 /pmc/articles/PMC4575534/ /pubmed/26167947 http://dx.doi.org/10.1089/cbr.2015.1837 Text en © Albertoni et al. 2015; Published by Mary Ann Liebert, Inc. This Open Access article is distributed under the terms of the Creative Commons Attribution Noncommercial License (http://creativecommons.org/licenses/by-nc/4.0/) which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and the source are credited.
spellingShingle Original Articles
Albertoni, Claudio
Leoni, Barbara
Rosi, Antonio
D'Alessio, Valeria
Carollo, Valeria
Spagnoli, Luigi Giusto
van Echteld, Cees
De Santis, Rita
Radionuclide Therapy of Unresectable Tumors with AvidinOX and (90)Y-biotinDOTA: Tongue Cancer Paradigm
title Radionuclide Therapy of Unresectable Tumors with AvidinOX and (90)Y-biotinDOTA: Tongue Cancer Paradigm
title_full Radionuclide Therapy of Unresectable Tumors with AvidinOX and (90)Y-biotinDOTA: Tongue Cancer Paradigm
title_fullStr Radionuclide Therapy of Unresectable Tumors with AvidinOX and (90)Y-biotinDOTA: Tongue Cancer Paradigm
title_full_unstemmed Radionuclide Therapy of Unresectable Tumors with AvidinOX and (90)Y-biotinDOTA: Tongue Cancer Paradigm
title_short Radionuclide Therapy of Unresectable Tumors with AvidinOX and (90)Y-biotinDOTA: Tongue Cancer Paradigm
title_sort radionuclide therapy of unresectable tumors with avidinox and (90)y-biotindota: tongue cancer paradigm
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4575534/
https://www.ncbi.nlm.nih.gov/pubmed/26167947
http://dx.doi.org/10.1089/cbr.2015.1837
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