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A non-functional 5′ ALK fusion validated at the RNA level as a classical EML4-ALK that responds well to the novel ALK inhibitor ensartinib: A case report
BACKGROUND: Currently, many targeted drugs are approved for treatment of ALK fusion non-small cell lung cancer. However, it has been previously assumed that patients with 5′ non-oncogenic kinase (5′ NOK) fusion detected by DNA next-generation sequencing (NGS) would not benefit from ALK inhibitors be...
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/PMC9582288/ https://www.ncbi.nlm.nih.gov/pubmed/36275795 http://dx.doi.org/10.3389/fmed.2022.979032 |
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author | Yang, Hong Li, Haojing Fang, Yu Li, Zhijun Zhu, Jianhua Liu, Huan Lu, Chao Zhang, Xiaoyan Ma, Tonghui Zhang, Cuiying |
author_facet | Yang, Hong Li, Haojing Fang, Yu Li, Zhijun Zhu, Jianhua Liu, Huan Lu, Chao Zhang, Xiaoyan Ma, Tonghui Zhang, Cuiying |
author_sort | Yang, Hong |
collection | PubMed |
description | BACKGROUND: Currently, many targeted drugs are approved for treatment of ALK fusion non-small cell lung cancer. However, it has been previously assumed that patients with 5′ non-oncogenic kinase (5′ NOK) fusion detected by DNA next-generation sequencing (NGS) would not benefit from ALK inhibitors because of lack of an intact kinase domain. CASE DESCRIPTION: A novel 5′ NOK fusion form, ALK-CYP27C1 (A19:C5), was detected by DNA NGS in surgical tissue specimens of a patient with recurrent lung adenosquamous carcinoma. The patient achieved 29 months of progression-free survival with ensartinib treatment. The results of RNA NGS from the same operative tissue identified EML4-ALK (E13:A20) fusion variant type I. CONCLUSION: This is the first case to provide real-world evidence of effective treatment of a patient with the 5′ NOK fusion form at the DNA level but functional EML4-ALK at the RNA level, illustrating the need for RNA testing in 5′ NOK patients. |
format | Online Article Text |
id | pubmed-9582288 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-95822882022-10-21 A non-functional 5′ ALK fusion validated at the RNA level as a classical EML4-ALK that responds well to the novel ALK inhibitor ensartinib: A case report Yang, Hong Li, Haojing Fang, Yu Li, Zhijun Zhu, Jianhua Liu, Huan Lu, Chao Zhang, Xiaoyan Ma, Tonghui Zhang, Cuiying Front Med (Lausanne) Medicine BACKGROUND: Currently, many targeted drugs are approved for treatment of ALK fusion non-small cell lung cancer. However, it has been previously assumed that patients with 5′ non-oncogenic kinase (5′ NOK) fusion detected by DNA next-generation sequencing (NGS) would not benefit from ALK inhibitors because of lack of an intact kinase domain. CASE DESCRIPTION: A novel 5′ NOK fusion form, ALK-CYP27C1 (A19:C5), was detected by DNA NGS in surgical tissue specimens of a patient with recurrent lung adenosquamous carcinoma. The patient achieved 29 months of progression-free survival with ensartinib treatment. The results of RNA NGS from the same operative tissue identified EML4-ALK (E13:A20) fusion variant type I. CONCLUSION: This is the first case to provide real-world evidence of effective treatment of a patient with the 5′ NOK fusion form at the DNA level but functional EML4-ALK at the RNA level, illustrating the need for RNA testing in 5′ NOK patients. Frontiers Media S.A. 2022-10-06 /pmc/articles/PMC9582288/ /pubmed/36275795 http://dx.doi.org/10.3389/fmed.2022.979032 Text en Copyright © 2022 Yang, Li, Fang, Li, Zhu, Liu, Lu, Zhang, Ma and Zhang. 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 | Medicine Yang, Hong Li, Haojing Fang, Yu Li, Zhijun Zhu, Jianhua Liu, Huan Lu, Chao Zhang, Xiaoyan Ma, Tonghui Zhang, Cuiying A non-functional 5′ ALK fusion validated at the RNA level as a classical EML4-ALK that responds well to the novel ALK inhibitor ensartinib: A case report |
title | A non-functional 5′ ALK fusion validated at the RNA level as a classical EML4-ALK that responds well to the novel ALK inhibitor ensartinib: A case report |
title_full | A non-functional 5′ ALK fusion validated at the RNA level as a classical EML4-ALK that responds well to the novel ALK inhibitor ensartinib: A case report |
title_fullStr | A non-functional 5′ ALK fusion validated at the RNA level as a classical EML4-ALK that responds well to the novel ALK inhibitor ensartinib: A case report |
title_full_unstemmed | A non-functional 5′ ALK fusion validated at the RNA level as a classical EML4-ALK that responds well to the novel ALK inhibitor ensartinib: A case report |
title_short | A non-functional 5′ ALK fusion validated at the RNA level as a classical EML4-ALK that responds well to the novel ALK inhibitor ensartinib: A case report |
title_sort | non-functional 5′ alk fusion validated at the rna level as a classical eml4-alk that responds well to the novel alk inhibitor ensartinib: a case report |
topic | Medicine |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9582288/ https://www.ncbi.nlm.nih.gov/pubmed/36275795 http://dx.doi.org/10.3389/fmed.2022.979032 |
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