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Combining Radiation Therapy with Immune Checkpoint Blockade for Central Nervous System Malignancies
Malignancies of the central nervous system (CNS), particularly glioblastoma and brain metastases from a variety of disease sites, are difficult to treat despite advances in multimodality approaches consisting of surgery, chemotherapy, and radiation therapy (RT). Recent successes of immunotherapeutic...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5053992/ https://www.ncbi.nlm.nih.gov/pubmed/27774435 http://dx.doi.org/10.3389/fonc.2016.00212 |
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author | D’Souza, Neil M. Fang, Penny Logan, Jennifer Yang, Jinzhong Jiang, Wen Li, Jing |
author_facet | D’Souza, Neil M. Fang, Penny Logan, Jennifer Yang, Jinzhong Jiang, Wen Li, Jing |
author_sort | D’Souza, Neil M. |
collection | PubMed |
description | Malignancies of the central nervous system (CNS), particularly glioblastoma and brain metastases from a variety of disease sites, are difficult to treat despite advances in multimodality approaches consisting of surgery, chemotherapy, and radiation therapy (RT). Recent successes of immunotherapeutic strategies including immune checkpoint blockade (ICB) via anti-PD-1 and anti-CTLA-4 antibodies against aggressive cancers, such as melanoma, non-small cell lung cancer, and renal cell carcinoma, have presented an exciting opportunity to translate these strategies for CNS malignancies. Moreover, via both localized cytotoxicity and systemic proinflammatory effects, the role of RT in enhancing antitumor immune response and, therefore, promoting tumor control is being re-examined, with several preclinical and clinical studies demonstrating potential synergistic effect of RT with ICB in the treatment of primary and metastatic CNS tumors. In this review, we highlight the preclinical evidence supporting the immunomodulatory effect of RT and discuss the rationales for its combination with ICB to promote antitumor immune response. We then outline the current clinical experience of combining RT with ICB in the treatment of multiple primary and metastatic brain tumors. Finally, we review advances in characterizing and modifying tumor radioimmunotherapy responses using biomarkers and microRNA (miRNA) that may potentially be used to guide clinical decision-making in the near future. |
format | Online Article Text |
id | pubmed-5053992 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-50539922016-10-21 Combining Radiation Therapy with Immune Checkpoint Blockade for Central Nervous System Malignancies D’Souza, Neil M. Fang, Penny Logan, Jennifer Yang, Jinzhong Jiang, Wen Li, Jing Front Oncol Oncology Malignancies of the central nervous system (CNS), particularly glioblastoma and brain metastases from a variety of disease sites, are difficult to treat despite advances in multimodality approaches consisting of surgery, chemotherapy, and radiation therapy (RT). Recent successes of immunotherapeutic strategies including immune checkpoint blockade (ICB) via anti-PD-1 and anti-CTLA-4 antibodies against aggressive cancers, such as melanoma, non-small cell lung cancer, and renal cell carcinoma, have presented an exciting opportunity to translate these strategies for CNS malignancies. Moreover, via both localized cytotoxicity and systemic proinflammatory effects, the role of RT in enhancing antitumor immune response and, therefore, promoting tumor control is being re-examined, with several preclinical and clinical studies demonstrating potential synergistic effect of RT with ICB in the treatment of primary and metastatic CNS tumors. In this review, we highlight the preclinical evidence supporting the immunomodulatory effect of RT and discuss the rationales for its combination with ICB to promote antitumor immune response. We then outline the current clinical experience of combining RT with ICB in the treatment of multiple primary and metastatic brain tumors. Finally, we review advances in characterizing and modifying tumor radioimmunotherapy responses using biomarkers and microRNA (miRNA) that may potentially be used to guide clinical decision-making in the near future. Frontiers Media S.A. 2016-10-07 /pmc/articles/PMC5053992/ /pubmed/27774435 http://dx.doi.org/10.3389/fonc.2016.00212 Text en Copyright © 2016 D’Souza, Fang, Logan, Yang, Jiang and Li. 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 D’Souza, Neil M. Fang, Penny Logan, Jennifer Yang, Jinzhong Jiang, Wen Li, Jing Combining Radiation Therapy with Immune Checkpoint Blockade for Central Nervous System Malignancies |
title | Combining Radiation Therapy with Immune Checkpoint Blockade for Central Nervous System Malignancies |
title_full | Combining Radiation Therapy with Immune Checkpoint Blockade for Central Nervous System Malignancies |
title_fullStr | Combining Radiation Therapy with Immune Checkpoint Blockade for Central Nervous System Malignancies |
title_full_unstemmed | Combining Radiation Therapy with Immune Checkpoint Blockade for Central Nervous System Malignancies |
title_short | Combining Radiation Therapy with Immune Checkpoint Blockade for Central Nervous System Malignancies |
title_sort | combining radiation therapy with immune checkpoint blockade for central nervous system malignancies |
topic | Oncology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5053992/ https://www.ncbi.nlm.nih.gov/pubmed/27774435 http://dx.doi.org/10.3389/fonc.2016.00212 |
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