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Combining Immunotherapy and Radiotherapy for Cancer Treatment: Current Challenges and Future Directions

Since the approval of anti-CTLA4 therapy (ipilimumab) for late-stage melanoma in 2011, the development of anticancer immunotherapy agents has thrived. The success of many immune-checkpoint inhibitors has drastically changed the landscape of cancer treatment. For some types of cancer, monotherapy for...

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Autores principales: Wang, Yifan, Deng, Weiye, Li, Nan, Neri, Shinya, Sharma, Amrish, Jiang, Wen, Lin, Steven H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5844965/
https://www.ncbi.nlm.nih.gov/pubmed/29556198
http://dx.doi.org/10.3389/fphar.2018.00185
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author Wang, Yifan
Deng, Weiye
Li, Nan
Neri, Shinya
Sharma, Amrish
Jiang, Wen
Lin, Steven H.
author_facet Wang, Yifan
Deng, Weiye
Li, Nan
Neri, Shinya
Sharma, Amrish
Jiang, Wen
Lin, Steven H.
author_sort Wang, Yifan
collection PubMed
description Since the approval of anti-CTLA4 therapy (ipilimumab) for late-stage melanoma in 2011, the development of anticancer immunotherapy agents has thrived. The success of many immune-checkpoint inhibitors has drastically changed the landscape of cancer treatment. For some types of cancer, monotherapy for targeting immune checkpoint pathways has proven more effective than traditional therapies, and combining immunotherapy with current treatment strategies may yield even better outcomes. Numerous preclinical studies have suggested that combining immunotherapy with radiotherapy could be a promising strategy for synergistic enhancement of treatment efficacy. Radiation delivered to the tumor site affects both tumor cells and surrounding stromal cells. Radiation-induced cancer cell damage exposes tumor-specific antigens that make them visible to immune surveillance and promotes the priming and activation of cytotoxic T cells. Radiation-induced modulation of the tumor microenvironment may also facilitate the recruitment and infiltration of immune cells. This unique relationship is the rationale for combining radiation with immune checkpoint blockade. Enhanced tumor recognition and immune cell targeting with checkpoint blockade may unleash the immune system to eliminate the cancer cells. However, challenges remain to be addressed to maximize the efficacy of this promising combination. Here we summarize the mechanisms of radiation and immune system interaction, and we discuss current challenges in radiation and immune checkpoint blockade therapy and possible future approaches to boost this combination.
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spelling pubmed-58449652018-03-19 Combining Immunotherapy and Radiotherapy for Cancer Treatment: Current Challenges and Future Directions Wang, Yifan Deng, Weiye Li, Nan Neri, Shinya Sharma, Amrish Jiang, Wen Lin, Steven H. Front Pharmacol Pharmacology Since the approval of anti-CTLA4 therapy (ipilimumab) for late-stage melanoma in 2011, the development of anticancer immunotherapy agents has thrived. The success of many immune-checkpoint inhibitors has drastically changed the landscape of cancer treatment. For some types of cancer, monotherapy for targeting immune checkpoint pathways has proven more effective than traditional therapies, and combining immunotherapy with current treatment strategies may yield even better outcomes. Numerous preclinical studies have suggested that combining immunotherapy with radiotherapy could be a promising strategy for synergistic enhancement of treatment efficacy. Radiation delivered to the tumor site affects both tumor cells and surrounding stromal cells. Radiation-induced cancer cell damage exposes tumor-specific antigens that make them visible to immune surveillance and promotes the priming and activation of cytotoxic T cells. Radiation-induced modulation of the tumor microenvironment may also facilitate the recruitment and infiltration of immune cells. This unique relationship is the rationale for combining radiation with immune checkpoint blockade. Enhanced tumor recognition and immune cell targeting with checkpoint blockade may unleash the immune system to eliminate the cancer cells. However, challenges remain to be addressed to maximize the efficacy of this promising combination. Here we summarize the mechanisms of radiation and immune system interaction, and we discuss current challenges in radiation and immune checkpoint blockade therapy and possible future approaches to boost this combination. Frontiers Media S.A. 2018-03-05 /pmc/articles/PMC5844965/ /pubmed/29556198 http://dx.doi.org/10.3389/fphar.2018.00185 Text en Copyright © 2018 Wang, Deng, Li, Neri, Sharma, Jiang and Lin. 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) and the copyright owner 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 Pharmacology
Wang, Yifan
Deng, Weiye
Li, Nan
Neri, Shinya
Sharma, Amrish
Jiang, Wen
Lin, Steven H.
Combining Immunotherapy and Radiotherapy for Cancer Treatment: Current Challenges and Future Directions
title Combining Immunotherapy and Radiotherapy for Cancer Treatment: Current Challenges and Future Directions
title_full Combining Immunotherapy and Radiotherapy for Cancer Treatment: Current Challenges and Future Directions
title_fullStr Combining Immunotherapy and Radiotherapy for Cancer Treatment: Current Challenges and Future Directions
title_full_unstemmed Combining Immunotherapy and Radiotherapy for Cancer Treatment: Current Challenges and Future Directions
title_short Combining Immunotherapy and Radiotherapy for Cancer Treatment: Current Challenges and Future Directions
title_sort combining immunotherapy and radiotherapy for cancer treatment: current challenges and future directions
topic Pharmacology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5844965/
https://www.ncbi.nlm.nih.gov/pubmed/29556198
http://dx.doi.org/10.3389/fphar.2018.00185
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