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Correlation between gene mutation status and clinicopathologic features in early multiple primary lung cancer
OBJECTIVE: To understand the characteristics of genetic mutation in multiple primary lung cancer so as to guide clinical decisions in targeted therapy. METHODS: We analyzed a total of 265 tumors from 111 patients who underwent surgery for multiple lung cancers. Individual tumors were subjected to hi...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10130385/ https://www.ncbi.nlm.nih.gov/pubmed/37124493 http://dx.doi.org/10.3389/fonc.2023.1110259 |
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author | Teng, Fei Xu, Jian Wang, Jian Yang, Bo Wu, Yong-Zhong Jiang, Yue-Quan Wang, Zhi-Qiang |
author_facet | Teng, Fei Xu, Jian Wang, Jian Yang, Bo Wu, Yong-Zhong Jiang, Yue-Quan Wang, Zhi-Qiang |
author_sort | Teng, Fei |
collection | PubMed |
description | OBJECTIVE: To understand the characteristics of genetic mutation in multiple primary lung cancer so as to guide clinical decisions in targeted therapy. METHODS: We analyzed a total of 265 tumors from 111 patients who underwent surgery for multiple lung cancers. Individual tumors were subjected to histological evaluation and gene mutation analysis using ABI 7500 Fluorescence quantitative PCR. RESULTS: In this study, we analyzed demographic and clinical parameters such as age, gender, smoking, alcohol consumption, pathological type, number of nodules, and other details of 111 patients with early multiple primary lung cancer. We also compared the clinicopathologic characteristics of different populations based on the gene mutation status of pulmonary nodules. Subsequently, we performed a clinicopathological analysis of all 265 pulmonary nodules from these patients. Results showed significant differences in clinicopathological features of pulmonary nodules in different genetic mutations. CONCLUSION: This study revealed the gene mutation characteristics and clinicopathological features in early multiple primary lung cancer. We found that the gene mutation status between different nodules in patients with early multiple primary lung cancer was inconsistent in most cases. Therefore, the use of targeted therapy based on the genetic sequencing of only one nodule, is unreliable. We hope this study can be helpful in guiding clinical treatment decisions. |
format | Online Article Text |
id | pubmed-10130385 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-101303852023-04-27 Correlation between gene mutation status and clinicopathologic features in early multiple primary lung cancer Teng, Fei Xu, Jian Wang, Jian Yang, Bo Wu, Yong-Zhong Jiang, Yue-Quan Wang, Zhi-Qiang Front Oncol Oncology OBJECTIVE: To understand the characteristics of genetic mutation in multiple primary lung cancer so as to guide clinical decisions in targeted therapy. METHODS: We analyzed a total of 265 tumors from 111 patients who underwent surgery for multiple lung cancers. Individual tumors were subjected to histological evaluation and gene mutation analysis using ABI 7500 Fluorescence quantitative PCR. RESULTS: In this study, we analyzed demographic and clinical parameters such as age, gender, smoking, alcohol consumption, pathological type, number of nodules, and other details of 111 patients with early multiple primary lung cancer. We also compared the clinicopathologic characteristics of different populations based on the gene mutation status of pulmonary nodules. Subsequently, we performed a clinicopathological analysis of all 265 pulmonary nodules from these patients. Results showed significant differences in clinicopathological features of pulmonary nodules in different genetic mutations. CONCLUSION: This study revealed the gene mutation characteristics and clinicopathological features in early multiple primary lung cancer. We found that the gene mutation status between different nodules in patients with early multiple primary lung cancer was inconsistent in most cases. Therefore, the use of targeted therapy based on the genetic sequencing of only one nodule, is unreliable. We hope this study can be helpful in guiding clinical treatment decisions. Frontiers Media S.A. 2023-04-12 /pmc/articles/PMC10130385/ /pubmed/37124493 http://dx.doi.org/10.3389/fonc.2023.1110259 Text en Copyright © 2023 Teng, Xu, Wang, Yang, Wu, Jiang and Wang 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 Teng, Fei Xu, Jian Wang, Jian Yang, Bo Wu, Yong-Zhong Jiang, Yue-Quan Wang, Zhi-Qiang Correlation between gene mutation status and clinicopathologic features in early multiple primary lung cancer |
title | Correlation between gene mutation status and clinicopathologic features in early multiple primary lung cancer |
title_full | Correlation between gene mutation status and clinicopathologic features in early multiple primary lung cancer |
title_fullStr | Correlation between gene mutation status and clinicopathologic features in early multiple primary lung cancer |
title_full_unstemmed | Correlation between gene mutation status and clinicopathologic features in early multiple primary lung cancer |
title_short | Correlation between gene mutation status and clinicopathologic features in early multiple primary lung cancer |
title_sort | correlation between gene mutation status and clinicopathologic features in early multiple primary lung cancer |
topic | Oncology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10130385/ https://www.ncbi.nlm.nih.gov/pubmed/37124493 http://dx.doi.org/10.3389/fonc.2023.1110259 |
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