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Combination therapy with immune checkpoint inhibitors (ICIs); a new frontier

Recently, immune checkpoint inhibitors (ICIs) therapy has become a promising therapeutic strategy with encouraging therapeutic outcomes due to their durable anti-tumor effects. Though, tumor inherent or acquired resistance to ICIs accompanied with treatment-related toxicities hamper their clinical u...

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Autores principales: Vafaei, Somayeh, Zekiy, Angelina O., Khanamir, Ramadhan Ado, Zaman, Burhan Abdullah, Ghayourvahdat, Arman, Azimizonuzi, Hannaneh, Zamani, Majid
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8725311/
https://www.ncbi.nlm.nih.gov/pubmed/34980128
http://dx.doi.org/10.1186/s12935-021-02407-8
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author Vafaei, Somayeh
Zekiy, Angelina O.
Khanamir, Ramadhan Ado
Zaman, Burhan Abdullah
Ghayourvahdat, Arman
Azimizonuzi, Hannaneh
Zamani, Majid
author_facet Vafaei, Somayeh
Zekiy, Angelina O.
Khanamir, Ramadhan Ado
Zaman, Burhan Abdullah
Ghayourvahdat, Arman
Azimizonuzi, Hannaneh
Zamani, Majid
author_sort Vafaei, Somayeh
collection PubMed
description Recently, immune checkpoint inhibitors (ICIs) therapy has become a promising therapeutic strategy with encouraging therapeutic outcomes due to their durable anti-tumor effects. Though, tumor inherent or acquired resistance to ICIs accompanied with treatment-related toxicities hamper their clinical utility. Overall, about 60–70% of patients (e.g., melanoma and lung cancer) who received ICIs show no objective response to intervention. The resistance to ICIs mainly caused by alterations in the tumor microenvironment (TME), which in turn, supports angiogenesis and also blocks immune cell antitumor activities, facilitating tumor cells' evasion from host immunosurveillance. Thereby, it has been supposed and also validated that combination therapy with ICIs and other therapeutic means, ranging from chemoradiotherapy to targeted therapies as well as cancer vaccines, can capably compromise tumor resistance to immune checkpoint blocked therapy. Herein, we have focused on the therapeutic benefits of ICIs as a groundbreaking approach in the context of tumor immunotherapy and also deliver an overview concerning the therapeutic influences of the addition of ICIs to other modalities to circumvent tumor resistance to ICIs.
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spelling pubmed-87253112022-01-06 Combination therapy with immune checkpoint inhibitors (ICIs); a new frontier Vafaei, Somayeh Zekiy, Angelina O. Khanamir, Ramadhan Ado Zaman, Burhan Abdullah Ghayourvahdat, Arman Azimizonuzi, Hannaneh Zamani, Majid Cancer Cell Int Review Recently, immune checkpoint inhibitors (ICIs) therapy has become a promising therapeutic strategy with encouraging therapeutic outcomes due to their durable anti-tumor effects. Though, tumor inherent or acquired resistance to ICIs accompanied with treatment-related toxicities hamper their clinical utility. Overall, about 60–70% of patients (e.g., melanoma and lung cancer) who received ICIs show no objective response to intervention. The resistance to ICIs mainly caused by alterations in the tumor microenvironment (TME), which in turn, supports angiogenesis and also blocks immune cell antitumor activities, facilitating tumor cells' evasion from host immunosurveillance. Thereby, it has been supposed and also validated that combination therapy with ICIs and other therapeutic means, ranging from chemoradiotherapy to targeted therapies as well as cancer vaccines, can capably compromise tumor resistance to immune checkpoint blocked therapy. Herein, we have focused on the therapeutic benefits of ICIs as a groundbreaking approach in the context of tumor immunotherapy and also deliver an overview concerning the therapeutic influences of the addition of ICIs to other modalities to circumvent tumor resistance to ICIs. BioMed Central 2022-01-03 /pmc/articles/PMC8725311/ /pubmed/34980128 http://dx.doi.org/10.1186/s12935-021-02407-8 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://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
Vafaei, Somayeh
Zekiy, Angelina O.
Khanamir, Ramadhan Ado
Zaman, Burhan Abdullah
Ghayourvahdat, Arman
Azimizonuzi, Hannaneh
Zamani, Majid
Combination therapy with immune checkpoint inhibitors (ICIs); a new frontier
title Combination therapy with immune checkpoint inhibitors (ICIs); a new frontier
title_full Combination therapy with immune checkpoint inhibitors (ICIs); a new frontier
title_fullStr Combination therapy with immune checkpoint inhibitors (ICIs); a new frontier
title_full_unstemmed Combination therapy with immune checkpoint inhibitors (ICIs); a new frontier
title_short Combination therapy with immune checkpoint inhibitors (ICIs); a new frontier
title_sort combination therapy with immune checkpoint inhibitors (icis); a new frontier
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8725311/
https://www.ncbi.nlm.nih.gov/pubmed/34980128
http://dx.doi.org/10.1186/s12935-021-02407-8
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