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Tumor Burden and Immunotherapy: Impact on Immune Infiltration and Therapeutic Outcomes

Cancer immunotherapy has revolutionized the treatment landscape in medical oncology, but its efficacy has been variable across patients. Biomarkers to predict such differential response to immunotherapy include cytotoxic T lymphocyte infiltration, tumor mutational burden, and microsatellite instabil...

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Detalles Bibliográficos
Autores principales: Kim, Samuel I., Cassella, Christopher R., Byrne, Katelyn T.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7882695/
https://www.ncbi.nlm.nih.gov/pubmed/33597954
http://dx.doi.org/10.3389/fimmu.2020.629722
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author Kim, Samuel I.
Cassella, Christopher R.
Byrne, Katelyn T.
author_facet Kim, Samuel I.
Cassella, Christopher R.
Byrne, Katelyn T.
author_sort Kim, Samuel I.
collection PubMed
description Cancer immunotherapy has revolutionized the treatment landscape in medical oncology, but its efficacy has been variable across patients. Biomarkers to predict such differential response to immunotherapy include cytotoxic T lymphocyte infiltration, tumor mutational burden, and microsatellite instability. A growing number of studies also suggest that baseline tumor burden, or tumor size, predicts response to immunotherapy. In this review, we discuss the changes in immune profile and therapeutic responses that occur with increasing tumor size. We also overview therapeutic approaches to reduce tumor burden and favorably modulate the immune microenvironment of larger tumors.
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spelling pubmed-78826952021-02-16 Tumor Burden and Immunotherapy: Impact on Immune Infiltration and Therapeutic Outcomes Kim, Samuel I. Cassella, Christopher R. Byrne, Katelyn T. Front Immunol Immunology Cancer immunotherapy has revolutionized the treatment landscape in medical oncology, but its efficacy has been variable across patients. Biomarkers to predict such differential response to immunotherapy include cytotoxic T lymphocyte infiltration, tumor mutational burden, and microsatellite instability. A growing number of studies also suggest that baseline tumor burden, or tumor size, predicts response to immunotherapy. In this review, we discuss the changes in immune profile and therapeutic responses that occur with increasing tumor size. We also overview therapeutic approaches to reduce tumor burden and favorably modulate the immune microenvironment of larger tumors. Frontiers Media S.A. 2021-02-01 /pmc/articles/PMC7882695/ /pubmed/33597954 http://dx.doi.org/10.3389/fimmu.2020.629722 Text en Copyright © 2021 Kim, Cassella and Byrne 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(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 Immunology
Kim, Samuel I.
Cassella, Christopher R.
Byrne, Katelyn T.
Tumor Burden and Immunotherapy: Impact on Immune Infiltration and Therapeutic Outcomes
title Tumor Burden and Immunotherapy: Impact on Immune Infiltration and Therapeutic Outcomes
title_full Tumor Burden and Immunotherapy: Impact on Immune Infiltration and Therapeutic Outcomes
title_fullStr Tumor Burden and Immunotherapy: Impact on Immune Infiltration and Therapeutic Outcomes
title_full_unstemmed Tumor Burden and Immunotherapy: Impact on Immune Infiltration and Therapeutic Outcomes
title_short Tumor Burden and Immunotherapy: Impact on Immune Infiltration and Therapeutic Outcomes
title_sort tumor burden and immunotherapy: impact on immune infiltration and therapeutic outcomes
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7882695/
https://www.ncbi.nlm.nih.gov/pubmed/33597954
http://dx.doi.org/10.3389/fimmu.2020.629722
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