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Normal tissues toxicities triggered by combined anti-angiogenic and radiation therapies: hurdles might be ahead

BACKGROUND: Combined-modality therapy is a promising approach to improve the therapeutic index of radiotherapy. However, these improvements could come at the cost of increased toxicities. Clinical trials evaluating anti-tumour efficacy of bevacizumab combined with radiotherapy have encountered unexp...

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Autores principales: Mangoni, M, Vozenin, M-C, Biti, G, Deutsch, E
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3394974/
https://www.ncbi.nlm.nih.gov/pubmed/22691970
http://dx.doi.org/10.1038/bjc.2012.236
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author Mangoni, M
Vozenin, M-C
Biti, G
Deutsch, E
author_facet Mangoni, M
Vozenin, M-C
Biti, G
Deutsch, E
author_sort Mangoni, M
collection PubMed
description BACKGROUND: Combined-modality therapy is a promising approach to improve the therapeutic index of radiotherapy. However, these improvements could come at the cost of increased toxicities. Clinical trials evaluating anti-tumour efficacy of bevacizumab combined with radiotherapy have encountered unexpected side effects. This study is the first systematic evaluation of normal tissue toxicity triggered by anti-angiogenic agents combined with radiation therapy in mice. METHODS: Effect of a mouse anti-VEGF antibody was monitored on acute toxicity studying radiation-induced intestinal ulceration (12 Gy TBI); on subacute toxicity using a model of oral mucositis (16.5 Gy); on late radiation injuries by monitoring lung fibrosis (bleomycin and 19 Gy). RESULTS: Combination of irradiation with anti-VEGF antibody enhanced intestinal damages with severe epithelial ulcerations, had no adverse impact on oral mucositis and dramatically worsened the fibrotic picture induced by bleomycin and irradiation to the lung. INTERPRETATION: These reports bring to light the important questions about safety and underscore the need for appropriate preclinical modelling of the impact on normal tissues of novel drug–radiation regimens. Our findings also highlight the complexity of anti-VEGF action, which could in defined conditions exert tissue-specific protection. The findings indicate that the combination of targeted drugs with radiotherapy should be approached with caution.
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spelling pubmed-33949742013-07-10 Normal tissues toxicities triggered by combined anti-angiogenic and radiation therapies: hurdles might be ahead Mangoni, M Vozenin, M-C Biti, G Deutsch, E Br J Cancer Translational Therapeutics BACKGROUND: Combined-modality therapy is a promising approach to improve the therapeutic index of radiotherapy. However, these improvements could come at the cost of increased toxicities. Clinical trials evaluating anti-tumour efficacy of bevacizumab combined with radiotherapy have encountered unexpected side effects. This study is the first systematic evaluation of normal tissue toxicity triggered by anti-angiogenic agents combined with radiation therapy in mice. METHODS: Effect of a mouse anti-VEGF antibody was monitored on acute toxicity studying radiation-induced intestinal ulceration (12 Gy TBI); on subacute toxicity using a model of oral mucositis (16.5 Gy); on late radiation injuries by monitoring lung fibrosis (bleomycin and 19 Gy). RESULTS: Combination of irradiation with anti-VEGF antibody enhanced intestinal damages with severe epithelial ulcerations, had no adverse impact on oral mucositis and dramatically worsened the fibrotic picture induced by bleomycin and irradiation to the lung. INTERPRETATION: These reports bring to light the important questions about safety and underscore the need for appropriate preclinical modelling of the impact on normal tissues of novel drug–radiation regimens. Our findings also highlight the complexity of anti-VEGF action, which could in defined conditions exert tissue-specific protection. The findings indicate that the combination of targeted drugs with radiotherapy should be approached with caution. Nature Publishing Group 2012-07-10 2012-06-12 /pmc/articles/PMC3394974/ /pubmed/22691970 http://dx.doi.org/10.1038/bjc.2012.236 Text en Copyright © 2012 Cancer Research UK https://creativecommons.org/licenses/by-nc-sa/3.0/From twelve months after its original publication, this work is licensed under the Creative Commons Attribution-NonCommercial-Share Alike 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/3.0/
spellingShingle Translational Therapeutics
Mangoni, M
Vozenin, M-C
Biti, G
Deutsch, E
Normal tissues toxicities triggered by combined anti-angiogenic and radiation therapies: hurdles might be ahead
title Normal tissues toxicities triggered by combined anti-angiogenic and radiation therapies: hurdles might be ahead
title_full Normal tissues toxicities triggered by combined anti-angiogenic and radiation therapies: hurdles might be ahead
title_fullStr Normal tissues toxicities triggered by combined anti-angiogenic and radiation therapies: hurdles might be ahead
title_full_unstemmed Normal tissues toxicities triggered by combined anti-angiogenic and radiation therapies: hurdles might be ahead
title_short Normal tissues toxicities triggered by combined anti-angiogenic and radiation therapies: hurdles might be ahead
title_sort normal tissues toxicities triggered by combined anti-angiogenic and radiation therapies: hurdles might be ahead
topic Translational Therapeutics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3394974/
https://www.ncbi.nlm.nih.gov/pubmed/22691970
http://dx.doi.org/10.1038/bjc.2012.236
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