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Radiation for hematologic malignancies: from cell killing to immune cell priming

Over the past half-century, the role of radiotherapy has been revolutionized, in part, by a shift from intent to directly kill cancer cells to the goal of priming anti-tumor immune responses that attack both irradiated and non-irradiated tumors. Stimulation of anti-tumor immunity depends on the inte...

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Autores principales: Dabaja, Bouthaina, Spiotto, Michael
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10299853/
https://www.ncbi.nlm.nih.gov/pubmed/37384297
http://dx.doi.org/10.3389/fonc.2023.1205836
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author Dabaja, Bouthaina
Spiotto, Michael
author_facet Dabaja, Bouthaina
Spiotto, Michael
author_sort Dabaja, Bouthaina
collection PubMed
description Over the past half-century, the role of radiotherapy has been revolutionized, in part, by a shift from intent to directly kill cancer cells to the goal of priming anti-tumor immune responses that attack both irradiated and non-irradiated tumors. Stimulation of anti-tumor immunity depends on the interplay between radiation, the tumor microenvironment, and the host immune system, which is a burgeoning concept in cancer immunology. While the interplay of radiotherapy and the immune system has been primarily studied in solid tumors, we are beginning to understand this interplay in hematological malignancies. The intent of this review is to lead readers through some of the important recent advances in immunotherapy and adoptive cell therapy, highlighting the best available evidence in support of incorporating radiation therapy and immunotherapy into the treatment of hematological malignancies. Evidence is presented regarding how radiation therapy ‘converses’ with the immune system to stimulate and enhance anti-tumor immune responses. This pro-immunogenic role of radiotherapy can be combined with monoclonal antibodies, cytokines and/or other immunostimulatory agents to enhance the regression of hematological malignancies. Furthermore, we will discuss how radiotherapy facilitates the effectiveness of cellular immunotherapies by acting as a “bridge” that facilitated CAR T cell engraftment and activity. These initial studies suggest radiotherapy may help catalyze a shift from using chemotherapy-intensive treatment to treatment that is “chemo-free” by combining with immunotherapy to target both the radiated and non-irradiated disease sites. This “journey” has opened the door for novel uses of radiotherapy in hematological malignancies due to its ability to prime anti-tumor immune responses which can augment immunotherapy and adoptive cell-based therapy.
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spelling pubmed-102998532023-06-28 Radiation for hematologic malignancies: from cell killing to immune cell priming Dabaja, Bouthaina Spiotto, Michael Front Oncol Oncology Over the past half-century, the role of radiotherapy has been revolutionized, in part, by a shift from intent to directly kill cancer cells to the goal of priming anti-tumor immune responses that attack both irradiated and non-irradiated tumors. Stimulation of anti-tumor immunity depends on the interplay between radiation, the tumor microenvironment, and the host immune system, which is a burgeoning concept in cancer immunology. While the interplay of radiotherapy and the immune system has been primarily studied in solid tumors, we are beginning to understand this interplay in hematological malignancies. The intent of this review is to lead readers through some of the important recent advances in immunotherapy and adoptive cell therapy, highlighting the best available evidence in support of incorporating radiation therapy and immunotherapy into the treatment of hematological malignancies. Evidence is presented regarding how radiation therapy ‘converses’ with the immune system to stimulate and enhance anti-tumor immune responses. This pro-immunogenic role of radiotherapy can be combined with monoclonal antibodies, cytokines and/or other immunostimulatory agents to enhance the regression of hematological malignancies. Furthermore, we will discuss how radiotherapy facilitates the effectiveness of cellular immunotherapies by acting as a “bridge” that facilitated CAR T cell engraftment and activity. These initial studies suggest radiotherapy may help catalyze a shift from using chemotherapy-intensive treatment to treatment that is “chemo-free” by combining with immunotherapy to target both the radiated and non-irradiated disease sites. This “journey” has opened the door for novel uses of radiotherapy in hematological malignancies due to its ability to prime anti-tumor immune responses which can augment immunotherapy and adoptive cell-based therapy. Frontiers Media S.A. 2023-06-13 /pmc/articles/PMC10299853/ /pubmed/37384297 http://dx.doi.org/10.3389/fonc.2023.1205836 Text en Copyright © 2023 Dabaja and Spiotto https://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) and the copyright owner(s) 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
Dabaja, Bouthaina
Spiotto, Michael
Radiation for hematologic malignancies: from cell killing to immune cell priming
title Radiation for hematologic malignancies: from cell killing to immune cell priming
title_full Radiation for hematologic malignancies: from cell killing to immune cell priming
title_fullStr Radiation for hematologic malignancies: from cell killing to immune cell priming
title_full_unstemmed Radiation for hematologic malignancies: from cell killing to immune cell priming
title_short Radiation for hematologic malignancies: from cell killing to immune cell priming
title_sort radiation for hematologic malignancies: from cell killing to immune cell priming
topic Oncology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10299853/
https://www.ncbi.nlm.nih.gov/pubmed/37384297
http://dx.doi.org/10.3389/fonc.2023.1205836
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