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Non-small cell lung cancer with MET exon 14 skipping alteration responding to immunotherapy: a case report

Immunotherapy has been proved to be a promising candidate for advanced non-small cell lung cancer (NSCLC). Despite MET mutations are regarded as an independent factor of programmed death ligand 1 (PD-L1) high expression, the efficacy of immune checkpoint inhibitors (ICIs) across NSCLC harboring Mese...

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Autores principales: Chen, Zhuxing, Zhu, Feng, Li, Caichen, Li, Jianfu, Cheng, Bo, Xiong, Shan, Zhong, Ran, Liang, Wenhua, He, Jianxing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: AME Publishing Company 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8033371/
https://www.ncbi.nlm.nih.gov/pubmed/33842645
http://dx.doi.org/10.21037/atm-20-6829
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author Chen, Zhuxing
Zhu, Feng
Li, Caichen
Li, Jianfu
Cheng, Bo
Xiong, Shan
Zhong, Ran
Liang, Wenhua
He, Jianxing
author_facet Chen, Zhuxing
Zhu, Feng
Li, Caichen
Li, Jianfu
Cheng, Bo
Xiong, Shan
Zhong, Ran
Liang, Wenhua
He, Jianxing
author_sort Chen, Zhuxing
collection PubMed
description Immunotherapy has been proved to be a promising candidate for advanced non-small cell lung cancer (NSCLC). Despite MET mutations are regarded as an independent factor of programmed death ligand 1 (PD-L1) high expression, the efficacy of immune checkpoint inhibitors (ICIs) across NSCLC harboring Mesenchymal-epithelial transition factor exon 14 skipping alteration (METex14) is still uncleared. Moreover, when the resistance of PD-1 antibody occurs, the questions of how to interpret the resistance and how to overcome the resistance are worth exploring. We report a case of NSCLC with METex14 developed a right femoral metastasis after responding well to neoadjuvant immunotherapy, a successful lobectomy, and adjuvant immunotherapy. The subsequent attempts of MET targeted inhibitor, concurrent chemoradiotherapy, and notably programmed cell death protein 1 (PD-1) antibody plus vascular endothelial growth factor receptor tyrosine kinase inhibitor (VEGFR-TKI) failed to prevent disease progression. However, a regimen of anti-PD-1 plus anti-cytotoxic t-lymphocyte associated protein 4 (CTLA-4) reversed the progression to a complete response. This case shows that METex14 had a significant response to immunotherapy, which would be especially beneficial for those who developed targeted therapy resistance. Importantly, this is the first case reporting that salvage CTLA-4 antibody and PD-1 antibody could reverse the progression in NSCLC harboring METex14 when the anti-PD-1 resistance occurred.
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spelling pubmed-80333712021-04-09 Non-small cell lung cancer with MET exon 14 skipping alteration responding to immunotherapy: a case report Chen, Zhuxing Zhu, Feng Li, Caichen Li, Jianfu Cheng, Bo Xiong, Shan Zhong, Ran Liang, Wenhua He, Jianxing Ann Transl Med Case Report Immunotherapy has been proved to be a promising candidate for advanced non-small cell lung cancer (NSCLC). Despite MET mutations are regarded as an independent factor of programmed death ligand 1 (PD-L1) high expression, the efficacy of immune checkpoint inhibitors (ICIs) across NSCLC harboring Mesenchymal-epithelial transition factor exon 14 skipping alteration (METex14) is still uncleared. Moreover, when the resistance of PD-1 antibody occurs, the questions of how to interpret the resistance and how to overcome the resistance are worth exploring. We report a case of NSCLC with METex14 developed a right femoral metastasis after responding well to neoadjuvant immunotherapy, a successful lobectomy, and adjuvant immunotherapy. The subsequent attempts of MET targeted inhibitor, concurrent chemoradiotherapy, and notably programmed cell death protein 1 (PD-1) antibody plus vascular endothelial growth factor receptor tyrosine kinase inhibitor (VEGFR-TKI) failed to prevent disease progression. However, a regimen of anti-PD-1 plus anti-cytotoxic t-lymphocyte associated protein 4 (CTLA-4) reversed the progression to a complete response. This case shows that METex14 had a significant response to immunotherapy, which would be especially beneficial for those who developed targeted therapy resistance. Importantly, this is the first case reporting that salvage CTLA-4 antibody and PD-1 antibody could reverse the progression in NSCLC harboring METex14 when the anti-PD-1 resistance occurred. AME Publishing Company 2021-03 /pmc/articles/PMC8033371/ /pubmed/33842645 http://dx.doi.org/10.21037/atm-20-6829 Text en 2021 Annals of Translational Medicine. All rights reserved. https://creativecommons.org/licenses/by-nc-nd/4.0/Open Access Statement: This is an Open Access article distributed in accordance with the Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License (CC BY-NC-ND 4.0), which permits the non-commercial replication and distribution of the article with the strict proviso that no changes or edits are made and the original work is properly cited (including links to both the formal publication through the relevant DOI and the license). See: https://creativecommons.org/licenses/by-nc-nd/4.0 (https://creativecommons.org/licenses/by-nc-nd/4.0/) .
spellingShingle Case Report
Chen, Zhuxing
Zhu, Feng
Li, Caichen
Li, Jianfu
Cheng, Bo
Xiong, Shan
Zhong, Ran
Liang, Wenhua
He, Jianxing
Non-small cell lung cancer with MET exon 14 skipping alteration responding to immunotherapy: a case report
title Non-small cell lung cancer with MET exon 14 skipping alteration responding to immunotherapy: a case report
title_full Non-small cell lung cancer with MET exon 14 skipping alteration responding to immunotherapy: a case report
title_fullStr Non-small cell lung cancer with MET exon 14 skipping alteration responding to immunotherapy: a case report
title_full_unstemmed Non-small cell lung cancer with MET exon 14 skipping alteration responding to immunotherapy: a case report
title_short Non-small cell lung cancer with MET exon 14 skipping alteration responding to immunotherapy: a case report
title_sort non-small cell lung cancer with met exon 14 skipping alteration responding to immunotherapy: a case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8033371/
https://www.ncbi.nlm.nih.gov/pubmed/33842645
http://dx.doi.org/10.21037/atm-20-6829
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