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Dosimetric evaluation of radionuclides for VCAM-1-targeted radionuclide therapy of early brain metastases

Brain metastases develop frequently in patients with breast cancer, and present a pressing therapeutic challenge. Expression of vascular cell adhesion molecule 1 (VCAM-1) is upregulated on brain endothelial cells during the early stages of metastasis and provides a target for the detection and treat...

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Autores principales: Falzone, Nadia, Ackerman, Nicole L., Rosales, Liset de la Fuente, Bernal, Mario A., Liu, Xiaoxuan, Peeters, Sarah GJA, Soto, Manuel Sarmiento, Corroyer-Dulmont, Aurélien, Bernaudin, Myriam, Grimoin, Elisa, Touzani, Omar, Sibson, Nicola R., Vallis, Katherine A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Ivyspring International Publisher 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5743475/
https://www.ncbi.nlm.nih.gov/pubmed/29290808
http://dx.doi.org/10.7150/thno.22217
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author Falzone, Nadia
Ackerman, Nicole L.
Rosales, Liset de la Fuente
Bernal, Mario A.
Liu, Xiaoxuan
Peeters, Sarah GJA
Soto, Manuel Sarmiento
Corroyer-Dulmont, Aurélien
Bernaudin, Myriam
Grimoin, Elisa
Touzani, Omar
Sibson, Nicola R.
Vallis, Katherine A.
author_facet Falzone, Nadia
Ackerman, Nicole L.
Rosales, Liset de la Fuente
Bernal, Mario A.
Liu, Xiaoxuan
Peeters, Sarah GJA
Soto, Manuel Sarmiento
Corroyer-Dulmont, Aurélien
Bernaudin, Myriam
Grimoin, Elisa
Touzani, Omar
Sibson, Nicola R.
Vallis, Katherine A.
author_sort Falzone, Nadia
collection PubMed
description Brain metastases develop frequently in patients with breast cancer, and present a pressing therapeutic challenge. Expression of vascular cell adhesion molecule 1 (VCAM-1) is upregulated on brain endothelial cells during the early stages of metastasis and provides a target for the detection and treatment of early brain metastases. The aim of this study was to use a model of early brain metastasis to evaluate the efficacy of α-emitting radionuclides, (149)Tb,( 211)At, (212)Pb, (213)Bi and( 225)Ac; β-emitting radionuclides, (90)Y,( 161)Tb and (177)Lu; and Auger electron (AE)-emitters (67)Ga, (89)Zr, (111)In and (124)I, for targeted radionuclide therapy (TRT). METHODS: Histologic sections and two photon microscopy of mouse brain parenchyma were used to inform a cylindrical vessel geometry using the Geant4 general purpose Monte Carlo (MC) toolkit with the Geant4-DNA low energy physics models. Energy deposition was evaluated as a radial function and the resulting phase spaces were superimposed on a DNA model to estimate double-strand break (DSB) yields for representative β- and α-emitters, (177)Lu and (212)Pb. Relative biological effectiveness (RBE) values were determined by only evaluating DNA damage due to physical interactions. RESULTS: (177)Lu produced 2.69 ± 0.08 DSB per GbpGy, without significant variation from the lumen of the vessel to a radius of 100 µm. The DSB yield of (212)Pb included two local maxima produced by the 6.1 MeV and 8.8 MeV α-emissions from decay products, (212)Bi and (212)Po, with yields of 7.64 ± 0.12 and 9.15 ± 0.24 per GbpGy, respectively. Given its higher DSB yield (212)Pb may be more effective for short range targeting of early micrometastatic lesions than (177)Lu. CONCLUSION: MC simulation of a model of early brain metastases provides invaluable insight into the potential efficacy of α-, β- and AE-emitting radionuclides for TRT. (212)Pb, which has the attributes of a theranostic radionuclide since it can be used for SPECT imaging, showed a favorable dose profile and RBE.
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spelling pubmed-57434752018-01-01 Dosimetric evaluation of radionuclides for VCAM-1-targeted radionuclide therapy of early brain metastases Falzone, Nadia Ackerman, Nicole L. Rosales, Liset de la Fuente Bernal, Mario A. Liu, Xiaoxuan Peeters, Sarah GJA Soto, Manuel Sarmiento Corroyer-Dulmont, Aurélien Bernaudin, Myriam Grimoin, Elisa Touzani, Omar Sibson, Nicola R. Vallis, Katherine A. Theranostics Research Paper Brain metastases develop frequently in patients with breast cancer, and present a pressing therapeutic challenge. Expression of vascular cell adhesion molecule 1 (VCAM-1) is upregulated on brain endothelial cells during the early stages of metastasis and provides a target for the detection and treatment of early brain metastases. The aim of this study was to use a model of early brain metastasis to evaluate the efficacy of α-emitting radionuclides, (149)Tb,( 211)At, (212)Pb, (213)Bi and( 225)Ac; β-emitting radionuclides, (90)Y,( 161)Tb and (177)Lu; and Auger electron (AE)-emitters (67)Ga, (89)Zr, (111)In and (124)I, for targeted radionuclide therapy (TRT). METHODS: Histologic sections and two photon microscopy of mouse brain parenchyma were used to inform a cylindrical vessel geometry using the Geant4 general purpose Monte Carlo (MC) toolkit with the Geant4-DNA low energy physics models. Energy deposition was evaluated as a radial function and the resulting phase spaces were superimposed on a DNA model to estimate double-strand break (DSB) yields for representative β- and α-emitters, (177)Lu and (212)Pb. Relative biological effectiveness (RBE) values were determined by only evaluating DNA damage due to physical interactions. RESULTS: (177)Lu produced 2.69 ± 0.08 DSB per GbpGy, without significant variation from the lumen of the vessel to a radius of 100 µm. The DSB yield of (212)Pb included two local maxima produced by the 6.1 MeV and 8.8 MeV α-emissions from decay products, (212)Bi and (212)Po, with yields of 7.64 ± 0.12 and 9.15 ± 0.24 per GbpGy, respectively. Given its higher DSB yield (212)Pb may be more effective for short range targeting of early micrometastatic lesions than (177)Lu. CONCLUSION: MC simulation of a model of early brain metastases provides invaluable insight into the potential efficacy of α-, β- and AE-emitting radionuclides for TRT. (212)Pb, which has the attributes of a theranostic radionuclide since it can be used for SPECT imaging, showed a favorable dose profile and RBE. Ivyspring International Publisher 2018-01-01 /pmc/articles/PMC5743475/ /pubmed/29290808 http://dx.doi.org/10.7150/thno.22217 Text en © Ivyspring International Publisher This is an open access article distributed under the terms of the Creative Commons Attribution (CC BY-NC) license (https://creativecommons.org/licenses/by-nc/4.0/). See http://ivyspring.com/terms for full terms and conditions.
spellingShingle Research Paper
Falzone, Nadia
Ackerman, Nicole L.
Rosales, Liset de la Fuente
Bernal, Mario A.
Liu, Xiaoxuan
Peeters, Sarah GJA
Soto, Manuel Sarmiento
Corroyer-Dulmont, Aurélien
Bernaudin, Myriam
Grimoin, Elisa
Touzani, Omar
Sibson, Nicola R.
Vallis, Katherine A.
Dosimetric evaluation of radionuclides for VCAM-1-targeted radionuclide therapy of early brain metastases
title Dosimetric evaluation of radionuclides for VCAM-1-targeted radionuclide therapy of early brain metastases
title_full Dosimetric evaluation of radionuclides for VCAM-1-targeted radionuclide therapy of early brain metastases
title_fullStr Dosimetric evaluation of radionuclides for VCAM-1-targeted radionuclide therapy of early brain metastases
title_full_unstemmed Dosimetric evaluation of radionuclides for VCAM-1-targeted radionuclide therapy of early brain metastases
title_short Dosimetric evaluation of radionuclides for VCAM-1-targeted radionuclide therapy of early brain metastases
title_sort dosimetric evaluation of radionuclides for vcam-1-targeted radionuclide therapy of early brain metastases
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5743475/
https://www.ncbi.nlm.nih.gov/pubmed/29290808
http://dx.doi.org/10.7150/thno.22217
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