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The Prevalence and Concurrent Pathogenic Mutations of KRAS(G12C) in Northeast Chinese Non-small-cell Lung Cancer Patients
OBJECTIVE: KRAS mutation is one of important driver genes in non-small-cell lung cancer (NSCLC) and the patients with KRAS(G12C) mutations benefit from the inhibitor AMG510. However, the frequency, concurrent pathogenic mutations, and clinical characteristic of KRAS(G12C) is unknown in the NSCLC pop...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7979353/ https://www.ncbi.nlm.nih.gov/pubmed/33758543 http://dx.doi.org/10.2147/CMAR.S282617 |
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author | Liu, Yan Li, Hui Zhu, Jing Zhang, Yang Liu, Xianhong Li, Rixin Zhang, Qiang Cheng, Ying |
author_facet | Liu, Yan Li, Hui Zhu, Jing Zhang, Yang Liu, Xianhong Li, Rixin Zhang, Qiang Cheng, Ying |
author_sort | Liu, Yan |
collection | PubMed |
description | OBJECTIVE: KRAS mutation is one of important driver genes in non-small-cell lung cancer (NSCLC) and the patients with KRAS(G12C) mutations benefit from the inhibitor AMG510. However, the frequency, concurrent pathogenic mutations, and clinical characteristic of KRAS(G12C) is unknown in the NSCLC population of Northeast China. METHODS: The retrospective analysis was derived from 431 NSCLC patients in Jilin Cancer Hospital between January 2018 and June 2019. The mutation frequency and concurrent mutations of KRAS(G12C) in tumor or peripheral blood was detected by next-generation sequencing (NGS). RESULTS: The RAS mutant rate was observed in 10.7% (46/431) of this cohort. All RAS-driver cancers are caused by mutations in the KRAS isoform, while the NRAS and HRAS isoforms were not detected. Among KRAS-mutant patients, 42 (91.3%) showed exon 2 mutation in 12 codon and 13 codon. KRAS(G12C) showed a 4.6% (20/431) mutation rate in this cohort and the highest frequency (43.5%, 20/46) in KRAS-mutant-positive patients. There was no difference between tumor tissue and plasma in terms of either KRAS or KRAS(G12C) mutation. The most frequent co-occurrence mutations with KRAS(G12C) were TP53, followed by PTEN. Furthermore, KRAS(G12C) was exclusive with STK11 mutation. KRAS(G12C) mutation was associated with age, disease stage, and smoking status (P=0.024; P=0.02; P=0.006), smoking remained an independent factor for KRAS(G12C) mutation (P=0.037), and higher mutation frequency in patients older than 60, stage I–III, or smoking in NSCLC (P=0.0151, P=0.0343, P=0.0046, respectively). CONCLUSION: KRAS mutation was the only isoforms of RAS family, of these 43.5% harbored the KRAS(G12C) subtype in northeastern Chinese NSCLC patients. KRAS(G12C) is associated with age, pathological stage and smoking status, more commonly harbored TP53/PTEN mutations, and providing more genome profile for targeted therapy in local clinical practice. |
format | Online Article Text |
id | pubmed-7979353 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Dove |
record_format | MEDLINE/PubMed |
spelling | pubmed-79793532021-03-22 The Prevalence and Concurrent Pathogenic Mutations of KRAS(G12C) in Northeast Chinese Non-small-cell Lung Cancer Patients Liu, Yan Li, Hui Zhu, Jing Zhang, Yang Liu, Xianhong Li, Rixin Zhang, Qiang Cheng, Ying Cancer Manag Res Original Research OBJECTIVE: KRAS mutation is one of important driver genes in non-small-cell lung cancer (NSCLC) and the patients with KRAS(G12C) mutations benefit from the inhibitor AMG510. However, the frequency, concurrent pathogenic mutations, and clinical characteristic of KRAS(G12C) is unknown in the NSCLC population of Northeast China. METHODS: The retrospective analysis was derived from 431 NSCLC patients in Jilin Cancer Hospital between January 2018 and June 2019. The mutation frequency and concurrent mutations of KRAS(G12C) in tumor or peripheral blood was detected by next-generation sequencing (NGS). RESULTS: The RAS mutant rate was observed in 10.7% (46/431) of this cohort. All RAS-driver cancers are caused by mutations in the KRAS isoform, while the NRAS and HRAS isoforms were not detected. Among KRAS-mutant patients, 42 (91.3%) showed exon 2 mutation in 12 codon and 13 codon. KRAS(G12C) showed a 4.6% (20/431) mutation rate in this cohort and the highest frequency (43.5%, 20/46) in KRAS-mutant-positive patients. There was no difference between tumor tissue and plasma in terms of either KRAS or KRAS(G12C) mutation. The most frequent co-occurrence mutations with KRAS(G12C) were TP53, followed by PTEN. Furthermore, KRAS(G12C) was exclusive with STK11 mutation. KRAS(G12C) mutation was associated with age, disease stage, and smoking status (P=0.024; P=0.02; P=0.006), smoking remained an independent factor for KRAS(G12C) mutation (P=0.037), and higher mutation frequency in patients older than 60, stage I–III, or smoking in NSCLC (P=0.0151, P=0.0343, P=0.0046, respectively). CONCLUSION: KRAS mutation was the only isoforms of RAS family, of these 43.5% harbored the KRAS(G12C) subtype in northeastern Chinese NSCLC patients. KRAS(G12C) is associated with age, pathological stage and smoking status, more commonly harbored TP53/PTEN mutations, and providing more genome profile for targeted therapy in local clinical practice. Dove 2021-03-15 /pmc/articles/PMC7979353/ /pubmed/33758543 http://dx.doi.org/10.2147/CMAR.S282617 Text en © 2021 Liu et al. http://creativecommons.org/licenses/by-nc/3.0/ This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php). |
spellingShingle | Original Research Liu, Yan Li, Hui Zhu, Jing Zhang, Yang Liu, Xianhong Li, Rixin Zhang, Qiang Cheng, Ying The Prevalence and Concurrent Pathogenic Mutations of KRAS(G12C) in Northeast Chinese Non-small-cell Lung Cancer Patients |
title | The Prevalence and Concurrent Pathogenic Mutations of KRAS(G12C) in Northeast Chinese Non-small-cell Lung Cancer Patients |
title_full | The Prevalence and Concurrent Pathogenic Mutations of KRAS(G12C) in Northeast Chinese Non-small-cell Lung Cancer Patients |
title_fullStr | The Prevalence and Concurrent Pathogenic Mutations of KRAS(G12C) in Northeast Chinese Non-small-cell Lung Cancer Patients |
title_full_unstemmed | The Prevalence and Concurrent Pathogenic Mutations of KRAS(G12C) in Northeast Chinese Non-small-cell Lung Cancer Patients |
title_short | The Prevalence and Concurrent Pathogenic Mutations of KRAS(G12C) in Northeast Chinese Non-small-cell Lung Cancer Patients |
title_sort | prevalence and concurrent pathogenic mutations of kras(g12c) in northeast chinese non-small-cell lung cancer patients |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7979353/ https://www.ncbi.nlm.nih.gov/pubmed/33758543 http://dx.doi.org/10.2147/CMAR.S282617 |
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