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Modern Radiotherapy Concepts and the Impact of Radiation on Immune Activation

Even though there is extensive research carried out in radiation oncology, most of the clinical studies focus on the effects of radiation on the local tumor tissue and deal with normal tissue side effects. The influence of dose fractionation and timing particularly with regard to immune activation i...

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Autores principales: Deloch, Lisa, Derer, Anja, Hartmann, Josefin, Frey, Benjamin, Fietkau, Rainer, Gaipl, Udo S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4913083/
https://www.ncbi.nlm.nih.gov/pubmed/27379203
http://dx.doi.org/10.3389/fonc.2016.00141
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author Deloch, Lisa
Derer, Anja
Hartmann, Josefin
Frey, Benjamin
Fietkau, Rainer
Gaipl, Udo S.
author_facet Deloch, Lisa
Derer, Anja
Hartmann, Josefin
Frey, Benjamin
Fietkau, Rainer
Gaipl, Udo S.
author_sort Deloch, Lisa
collection PubMed
description Even though there is extensive research carried out in radiation oncology, most of the clinical studies focus on the effects of radiation on the local tumor tissue and deal with normal tissue side effects. The influence of dose fractionation and timing particularly with regard to immune activation is not satisfactorily investigated so far. This review, therefore, summarizes current knowledge on concepts of modern radiotherapy (RT) and evaluates the potential of RT for immune activation. Focus is set on radiation-induced forms of tumor cell death and consecutively the immunogenicity of the tumor cells. The so-called non-targeted, abscopal effects can contribute to anti-tumor responses in a specific and systemic manner and possess the ability to target relapsing tumor cells as well as metastases. The impact of distinct RT concepts on immune activation is outlined and pre-clinical evidence and clinical observations on RT-induced immunity will be discussed. Knowledge on the radiosensitivity of immune cells as well as clinical evidence for enhanced immunity after RT will be considered. While stereotactic ablative body radiotherapy seem to have a beneficial outcome over classical RT fractionation in pre-clinical animal models, in vitro model systems suggest an advantage for classical fractionated RT for immune activation. Furthermore, the optimal approach may differ based on the tumor site and/or genetic signature. These facts highlight that clinical trials are urgently needed to identify whether high-dose RT is superior to induce anti-tumor immune responses compared to classical fractionated RT and in particular how the outcome is when RT is combined with immunotherapy in selected tumor entities.
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spelling pubmed-49130832016-07-04 Modern Radiotherapy Concepts and the Impact of Radiation on Immune Activation Deloch, Lisa Derer, Anja Hartmann, Josefin Frey, Benjamin Fietkau, Rainer Gaipl, Udo S. Front Oncol Oncology Even though there is extensive research carried out in radiation oncology, most of the clinical studies focus on the effects of radiation on the local tumor tissue and deal with normal tissue side effects. The influence of dose fractionation and timing particularly with regard to immune activation is not satisfactorily investigated so far. This review, therefore, summarizes current knowledge on concepts of modern radiotherapy (RT) and evaluates the potential of RT for immune activation. Focus is set on radiation-induced forms of tumor cell death and consecutively the immunogenicity of the tumor cells. The so-called non-targeted, abscopal effects can contribute to anti-tumor responses in a specific and systemic manner and possess the ability to target relapsing tumor cells as well as metastases. The impact of distinct RT concepts on immune activation is outlined and pre-clinical evidence and clinical observations on RT-induced immunity will be discussed. Knowledge on the radiosensitivity of immune cells as well as clinical evidence for enhanced immunity after RT will be considered. While stereotactic ablative body radiotherapy seem to have a beneficial outcome over classical RT fractionation in pre-clinical animal models, in vitro model systems suggest an advantage for classical fractionated RT for immune activation. Furthermore, the optimal approach may differ based on the tumor site and/or genetic signature. These facts highlight that clinical trials are urgently needed to identify whether high-dose RT is superior to induce anti-tumor immune responses compared to classical fractionated RT and in particular how the outcome is when RT is combined with immunotherapy in selected tumor entities. Frontiers Media S.A. 2016-06-20 /pmc/articles/PMC4913083/ /pubmed/27379203 http://dx.doi.org/10.3389/fonc.2016.00141 Text en Copyright © 2016 Deloch, Derer, Hartmann, Frey, Fietkau and Gaipl. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Oncology
Deloch, Lisa
Derer, Anja
Hartmann, Josefin
Frey, Benjamin
Fietkau, Rainer
Gaipl, Udo S.
Modern Radiotherapy Concepts and the Impact of Radiation on Immune Activation
title Modern Radiotherapy Concepts and the Impact of Radiation on Immune Activation
title_full Modern Radiotherapy Concepts and the Impact of Radiation on Immune Activation
title_fullStr Modern Radiotherapy Concepts and the Impact of Radiation on Immune Activation
title_full_unstemmed Modern Radiotherapy Concepts and the Impact of Radiation on Immune Activation
title_short Modern Radiotherapy Concepts and the Impact of Radiation on Immune Activation
title_sort modern radiotherapy concepts and the impact of radiation on immune activation
topic Oncology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4913083/
https://www.ncbi.nlm.nih.gov/pubmed/27379203
http://dx.doi.org/10.3389/fonc.2016.00141
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