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Current status and challenges of immunotherapy in ALK rearranged NSCLC
Rearrangements of the anaplastic lymphoma kinase (ALK) gene account for 5-6% in non-small cell lung cancer (NSCLC). ALK rearranged NSCLC is sensitive to ALK tyrosine kinase inhibitors (TKIs) but prone to drug resistance. Meanwhile, ALK rearranged NSCLC has poor response to single immunotherapy. Here...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9795041/ https://www.ncbi.nlm.nih.gov/pubmed/36591504 http://dx.doi.org/10.3389/fonc.2022.1016869 |
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author | Qi, Rongbin Yu, Yingying Shen, Mo Lv, Dongqing He, Susu |
author_facet | Qi, Rongbin Yu, Yingying Shen, Mo Lv, Dongqing He, Susu |
author_sort | Qi, Rongbin |
collection | PubMed |
description | Rearrangements of the anaplastic lymphoma kinase (ALK) gene account for 5-6% in non-small cell lung cancer (NSCLC). ALK rearranged NSCLC is sensitive to ALK tyrosine kinase inhibitors (TKIs) but prone to drug resistance. Meanwhile, ALK rearranged NSCLC has poor response to single immunotherapy. Here we mainly describe the immune escape mechanisms of ALK mutated NSCLC and the role of related biomarkers. Additionally, we collate and evaluate preclinical and clinical studies of novel immune combination regimens, and describe the prospects and perspectives for the in vivo application of novel immune technologies in patients with ALK rearranged NSCLC. |
format | Online Article Text |
id | pubmed-9795041 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-97950412022-12-29 Current status and challenges of immunotherapy in ALK rearranged NSCLC Qi, Rongbin Yu, Yingying Shen, Mo Lv, Dongqing He, Susu Front Oncol Oncology Rearrangements of the anaplastic lymphoma kinase (ALK) gene account for 5-6% in non-small cell lung cancer (NSCLC). ALK rearranged NSCLC is sensitive to ALK tyrosine kinase inhibitors (TKIs) but prone to drug resistance. Meanwhile, ALK rearranged NSCLC has poor response to single immunotherapy. Here we mainly describe the immune escape mechanisms of ALK mutated NSCLC and the role of related biomarkers. Additionally, we collate and evaluate preclinical and clinical studies of novel immune combination regimens, and describe the prospects and perspectives for the in vivo application of novel immune technologies in patients with ALK rearranged NSCLC. Frontiers Media S.A. 2022-12-14 /pmc/articles/PMC9795041/ /pubmed/36591504 http://dx.doi.org/10.3389/fonc.2022.1016869 Text en Copyright © 2022 Qi, Yu, Shen, Lv and He https://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 | Oncology Qi, Rongbin Yu, Yingying Shen, Mo Lv, Dongqing He, Susu Current status and challenges of immunotherapy in ALK rearranged NSCLC |
title | Current status and challenges of immunotherapy in ALK rearranged NSCLC |
title_full | Current status and challenges of immunotherapy in ALK rearranged NSCLC |
title_fullStr | Current status and challenges of immunotherapy in ALK rearranged NSCLC |
title_full_unstemmed | Current status and challenges of immunotherapy in ALK rearranged NSCLC |
title_short | Current status and challenges of immunotherapy in ALK rearranged NSCLC |
title_sort | current status and challenges of immunotherapy in alk rearranged nsclc |
topic | Oncology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9795041/ https://www.ncbi.nlm.nih.gov/pubmed/36591504 http://dx.doi.org/10.3389/fonc.2022.1016869 |
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