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Immunotherapy for Non-small Cell Lung Cancer: Current Landscape and Future Perspectives
Immune checkpoint inhibitors (ICIs) have shown remarkable benefit in the treatment of patients with non-small-cell lung cancer (NSCLC) and have emerged as an effective treatment option even in the first-line setting. ICIs can block inhibitory pathways that restrain the immune response against cancer...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Korean Association of Immunologists
2020
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7049584/ https://www.ncbi.nlm.nih.gov/pubmed/32158598 http://dx.doi.org/10.4110/in.2020.20.e10 |
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author | Lim, Sun Min Hong, Min Hee Kim, Hye Ryun |
author_facet | Lim, Sun Min Hong, Min Hee Kim, Hye Ryun |
author_sort | Lim, Sun Min |
collection | PubMed |
description | Immune checkpoint inhibitors (ICIs) have shown remarkable benefit in the treatment of patients with non-small-cell lung cancer (NSCLC) and have emerged as an effective treatment option even in the first-line setting. ICIs can block inhibitory pathways that restrain the immune response against cancer, restoring and sustaining antitumor immunity. Currently, there are 4 PD-1/PD-L1 blocking agents available in clinics, and immunotherapy-based regimen alone or in combination with chemotherapy is now preferred option. Combination trials assessing combination of ICIs with chemotherapy, targeted therapy and other immunotherapy are ongoing. Controversies remain regarding the use of ICIs in targetable oncogene-addicted subpopulations, but their initial treatment recommendations remained unchanged, with specific tyrosine kinase inhibitors as the choice. For the majority of patients without targetable driver oncogenes, deciding between therapeutic options can be difficult due to lack of direct cross-comparison studies. There are continuous efforts to find predictive biomarkers to find those who respond better to ICIs. PD-L1 protein expressions by immunohistochemistry and tumor mutational burden have emerged as most well-validated biomarkers in multiple clinical trials. However, there still is a need to improve patient selection, and to establish the most effective concurrent or sequential combination therapies in different NSCLC clinical settings. In this review, we will introduce currently used ICIs in NSCLC and analyze most recent trials, and finally discuss how, when and for whom ICIs can be used to provide promising avenues for lung cancer treatment. |
format | Online Article Text |
id | pubmed-7049584 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | The Korean Association of Immunologists |
record_format | MEDLINE/PubMed |
spelling | pubmed-70495842020-03-10 Immunotherapy for Non-small Cell Lung Cancer: Current Landscape and Future Perspectives Lim, Sun Min Hong, Min Hee Kim, Hye Ryun Immune Netw Review Article Immune checkpoint inhibitors (ICIs) have shown remarkable benefit in the treatment of patients with non-small-cell lung cancer (NSCLC) and have emerged as an effective treatment option even in the first-line setting. ICIs can block inhibitory pathways that restrain the immune response against cancer, restoring and sustaining antitumor immunity. Currently, there are 4 PD-1/PD-L1 blocking agents available in clinics, and immunotherapy-based regimen alone or in combination with chemotherapy is now preferred option. Combination trials assessing combination of ICIs with chemotherapy, targeted therapy and other immunotherapy are ongoing. Controversies remain regarding the use of ICIs in targetable oncogene-addicted subpopulations, but their initial treatment recommendations remained unchanged, with specific tyrosine kinase inhibitors as the choice. For the majority of patients without targetable driver oncogenes, deciding between therapeutic options can be difficult due to lack of direct cross-comparison studies. There are continuous efforts to find predictive biomarkers to find those who respond better to ICIs. PD-L1 protein expressions by immunohistochemistry and tumor mutational burden have emerged as most well-validated biomarkers in multiple clinical trials. However, there still is a need to improve patient selection, and to establish the most effective concurrent or sequential combination therapies in different NSCLC clinical settings. In this review, we will introduce currently used ICIs in NSCLC and analyze most recent trials, and finally discuss how, when and for whom ICIs can be used to provide promising avenues for lung cancer treatment. The Korean Association of Immunologists 2020-01-27 /pmc/articles/PMC7049584/ /pubmed/32158598 http://dx.doi.org/10.4110/in.2020.20.e10 Text en Copyright © 2020. The Korean Association of Immunologists https://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (https://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Review Article Lim, Sun Min Hong, Min Hee Kim, Hye Ryun Immunotherapy for Non-small Cell Lung Cancer: Current Landscape and Future Perspectives |
title | Immunotherapy for Non-small Cell Lung Cancer: Current Landscape and Future Perspectives |
title_full | Immunotherapy for Non-small Cell Lung Cancer: Current Landscape and Future Perspectives |
title_fullStr | Immunotherapy for Non-small Cell Lung Cancer: Current Landscape and Future Perspectives |
title_full_unstemmed | Immunotherapy for Non-small Cell Lung Cancer: Current Landscape and Future Perspectives |
title_short | Immunotherapy for Non-small Cell Lung Cancer: Current Landscape and Future Perspectives |
title_sort | immunotherapy for non-small cell lung cancer: current landscape and future perspectives |
topic | Review Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7049584/ https://www.ncbi.nlm.nih.gov/pubmed/32158598 http://dx.doi.org/10.4110/in.2020.20.e10 |
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