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Overcoming immunotherapy resistance in non-small cell lung cancer (NSCLC) - novel approaches and future outlook
Immunotherapy (IO) has revolutionized the therapy landscape of non-small cell lung cancer (NSCLC), significantly prolonging the overall survival (OS) of advanced stage patients. Over the recent years IO therapy has been broadly integrated into the first-line setting of non-oncogene driven NSCLC, eit...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7488475/ https://www.ncbi.nlm.nih.gov/pubmed/32917214 http://dx.doi.org/10.1186/s12943-020-01260-z |
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author | Horvath, Lena Thienpont, Bernard Zhao, Liyun Wolf, Dominik Pircher, Andreas |
author_facet | Horvath, Lena Thienpont, Bernard Zhao, Liyun Wolf, Dominik Pircher, Andreas |
author_sort | Horvath, Lena |
collection | PubMed |
description | Immunotherapy (IO) has revolutionized the therapy landscape of non-small cell lung cancer (NSCLC), significantly prolonging the overall survival (OS) of advanced stage patients. Over the recent years IO therapy has been broadly integrated into the first-line setting of non-oncogene driven NSCLC, either in combination with chemotherapy, or in selected patients with PD-L1(high) expression as monotherapy. Still, a significant proportion of patients suffer from disease progression. A better understanding of resistance mechanisms depicts a central goal to avoid or overcome IO resistance and to improve patient outcome. We here review major cellular and molecular pathways within the tumor microenvironment (TME) that may impact the evolution of IO resistance. We summarize upcoming treatment options after IO resistance including novel IO targets (e.g. RIG-I, STING) as well as interesting combinational approaches such as IO combined with anti-angiogenic agents or metabolic targets (e.g. IDO-1, adenosine signaling, arginase). By discussing the fundamental mode of action of IO within the TME, we aim to understand and manage IO resistance and to seed new ideas for effective therapeutic IO concepts. |
format | Online Article Text |
id | pubmed-7488475 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-74884752020-09-16 Overcoming immunotherapy resistance in non-small cell lung cancer (NSCLC) - novel approaches and future outlook Horvath, Lena Thienpont, Bernard Zhao, Liyun Wolf, Dominik Pircher, Andreas Mol Cancer Review Immunotherapy (IO) has revolutionized the therapy landscape of non-small cell lung cancer (NSCLC), significantly prolonging the overall survival (OS) of advanced stage patients. Over the recent years IO therapy has been broadly integrated into the first-line setting of non-oncogene driven NSCLC, either in combination with chemotherapy, or in selected patients with PD-L1(high) expression as monotherapy. Still, a significant proportion of patients suffer from disease progression. A better understanding of resistance mechanisms depicts a central goal to avoid or overcome IO resistance and to improve patient outcome. We here review major cellular and molecular pathways within the tumor microenvironment (TME) that may impact the evolution of IO resistance. We summarize upcoming treatment options after IO resistance including novel IO targets (e.g. RIG-I, STING) as well as interesting combinational approaches such as IO combined with anti-angiogenic agents or metabolic targets (e.g. IDO-1, adenosine signaling, arginase). By discussing the fundamental mode of action of IO within the TME, we aim to understand and manage IO resistance and to seed new ideas for effective therapeutic IO concepts. BioMed Central 2020-09-11 /pmc/articles/PMC7488475/ /pubmed/32917214 http://dx.doi.org/10.1186/s12943-020-01260-z Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Review Horvath, Lena Thienpont, Bernard Zhao, Liyun Wolf, Dominik Pircher, Andreas Overcoming immunotherapy resistance in non-small cell lung cancer (NSCLC) - novel approaches and future outlook |
title | Overcoming immunotherapy resistance in non-small cell lung cancer (NSCLC) - novel approaches and future outlook |
title_full | Overcoming immunotherapy resistance in non-small cell lung cancer (NSCLC) - novel approaches and future outlook |
title_fullStr | Overcoming immunotherapy resistance in non-small cell lung cancer (NSCLC) - novel approaches and future outlook |
title_full_unstemmed | Overcoming immunotherapy resistance in non-small cell lung cancer (NSCLC) - novel approaches and future outlook |
title_short | Overcoming immunotherapy resistance in non-small cell lung cancer (NSCLC) - novel approaches and future outlook |
title_sort | overcoming immunotherapy resistance in non-small cell lung cancer (nsclc) - novel approaches and future outlook |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7488475/ https://www.ncbi.nlm.nih.gov/pubmed/32917214 http://dx.doi.org/10.1186/s12943-020-01260-z |
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