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Combined Radionuclide Therapy and Immunotherapy for Treatment of Triple Negative Breast Cancer
Triple negative breast cancer (TNBC) is an aggressive subtype of the disease with poor clinical outcomes and limited therapeutic options. Immune checkpoint blockade (CP) has surged to the forefront of cancer therapies with widespread clinical success in a variety of cancer types. However, the percen...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8124136/ https://www.ncbi.nlm.nih.gov/pubmed/34063642 http://dx.doi.org/10.3390/ijms22094843 |
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author | Vito, Alyssa Rathmann, Stephanie Mercanti, Natalie El-Sayes, Nader Mossman, Karen Valliant, John |
author_facet | Vito, Alyssa Rathmann, Stephanie Mercanti, Natalie El-Sayes, Nader Mossman, Karen Valliant, John |
author_sort | Vito, Alyssa |
collection | PubMed |
description | Triple negative breast cancer (TNBC) is an aggressive subtype of the disease with poor clinical outcomes and limited therapeutic options. Immune checkpoint blockade (CP) has surged to the forefront of cancer therapies with widespread clinical success in a variety of cancer types. However, the percentage of TNBC patients that benefit from CP as a monotherapy is low, and clinical trials have shown the need for combined therapeutic modalities. Specifically, there has been interest in combining CP therapy with radiation therapy where clinical studies primarily with external beam have suggested their therapeutic synergy, contributing to the development of anti-tumor immunity. Here, we have developed a therapeutic platform combining radionuclide therapy (RT) and immunotherapy utilizing a radiolabeled biomolecule and CP in an E0771 murine TNBC tumor model. Survival studies show that while neither monotherapy is able to improve therapeutic outcomes, the combination of RT + CP extended overall survival. Histologic analysis showed that RT + CP increased necrotic tissue within the tumor and decreased levels of F4/80+ macrophages. Flow cytometry analysis of the peripheral blood also showed that RT + CP suppressed macrophages and myeloid-derived suppressive cells, both of which actively contribute to immune escape and tumor relapse. |
format | Online Article Text |
id | pubmed-8124136 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-81241362021-05-17 Combined Radionuclide Therapy and Immunotherapy for Treatment of Triple Negative Breast Cancer Vito, Alyssa Rathmann, Stephanie Mercanti, Natalie El-Sayes, Nader Mossman, Karen Valliant, John Int J Mol Sci Article Triple negative breast cancer (TNBC) is an aggressive subtype of the disease with poor clinical outcomes and limited therapeutic options. Immune checkpoint blockade (CP) has surged to the forefront of cancer therapies with widespread clinical success in a variety of cancer types. However, the percentage of TNBC patients that benefit from CP as a monotherapy is low, and clinical trials have shown the need for combined therapeutic modalities. Specifically, there has been interest in combining CP therapy with radiation therapy where clinical studies primarily with external beam have suggested their therapeutic synergy, contributing to the development of anti-tumor immunity. Here, we have developed a therapeutic platform combining radionuclide therapy (RT) and immunotherapy utilizing a radiolabeled biomolecule and CP in an E0771 murine TNBC tumor model. Survival studies show that while neither monotherapy is able to improve therapeutic outcomes, the combination of RT + CP extended overall survival. Histologic analysis showed that RT + CP increased necrotic tissue within the tumor and decreased levels of F4/80+ macrophages. Flow cytometry analysis of the peripheral blood also showed that RT + CP suppressed macrophages and myeloid-derived suppressive cells, both of which actively contribute to immune escape and tumor relapse. MDPI 2021-05-03 /pmc/articles/PMC8124136/ /pubmed/34063642 http://dx.doi.org/10.3390/ijms22094843 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Vito, Alyssa Rathmann, Stephanie Mercanti, Natalie El-Sayes, Nader Mossman, Karen Valliant, John Combined Radionuclide Therapy and Immunotherapy for Treatment of Triple Negative Breast Cancer |
title | Combined Radionuclide Therapy and Immunotherapy for Treatment of Triple Negative Breast Cancer |
title_full | Combined Radionuclide Therapy and Immunotherapy for Treatment of Triple Negative Breast Cancer |
title_fullStr | Combined Radionuclide Therapy and Immunotherapy for Treatment of Triple Negative Breast Cancer |
title_full_unstemmed | Combined Radionuclide Therapy and Immunotherapy for Treatment of Triple Negative Breast Cancer |
title_short | Combined Radionuclide Therapy and Immunotherapy for Treatment of Triple Negative Breast Cancer |
title_sort | combined radionuclide therapy and immunotherapy for treatment of triple negative breast cancer |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8124136/ https://www.ncbi.nlm.nih.gov/pubmed/34063642 http://dx.doi.org/10.3390/ijms22094843 |
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