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A meta-analysis of the association between BRAF mutation and nonsmall cell lung cancer
BACKGROUND: Previous studies investigating the association between BRAF mutations and nonsmall cell lung cancer (NSCLC) remain controversial. To address the issue, we performed an updated meta-analysis of related articles. METHODS: We conducted a comprehensive literature search in the electronic dat...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer Health
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5411210/ https://www.ncbi.nlm.nih.gov/pubmed/28383426 http://dx.doi.org/10.1097/MD.0000000000006552 |
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author | Cui, Guanghui Liu, Donglei Li, Weihao Fu, Xiao Liang, Youguang Li, Yuhang Shi, Wensong Chen, Xiaofang Zhao, Song |
author_facet | Cui, Guanghui Liu, Donglei Li, Weihao Fu, Xiao Liang, Youguang Li, Yuhang Shi, Wensong Chen, Xiaofang Zhao, Song |
author_sort | Cui, Guanghui |
collection | PubMed |
description | BACKGROUND: Previous studies investigating the association between BRAF mutations and nonsmall cell lung cancer (NSCLC) remain controversial. To address the issue, we performed an updated meta-analysis of related articles. METHODS: We conducted a comprehensive literature search in the electronic databases including ISI Science Citation Index, EMBASE, PubMed, and CNKI (up to January 2016). The odds ratios (ORs) and 95% confidence interval (CI) were assessed based on random-effects or fixed-effects models according to the heterogeneity of eligible studies. RESULTS: A total of 16 studies enrolled 11,711 patients with NSCLC were involved in the meta-analysis. The overall BRAF mutation rate was 2.6% (303/11,711). There was a significant association between BRAF mutations and adenocarcinomas (ADCs) in NSCLC compared with non-ADCs (OR = 3.96, 95% CI = 2.13–7.34, P < 0.0001). No significant difference was observed in smoking and stage in patients with BRAF mutations. However, a significant difference of BRAF mutation rate was observed between women and men (OR = 0.72, 95% CI = 0.55–0.95, P = 0.02). In addition, the BRAF(V600E) mutations were more frequent in women (OR = 0.45, 95% CI = 0.26–0.77, P = 0.004) and never smokers (OR = 0.12, 95% CI = 0.05–0.29, P < 0.00001). CONCLUSIONS: BRAF mutations in ADCS and female significantly increased the risk of NSCLC compared to non-ADCS and male, respectively. BRAFV(600E) mutation in NSCLC patients was significantly associated with female and nonsmokers. |
format | Online Article Text |
id | pubmed-5411210 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Wolters Kluwer Health |
record_format | MEDLINE/PubMed |
spelling | pubmed-54112102017-05-02 A meta-analysis of the association between BRAF mutation and nonsmall cell lung cancer Cui, Guanghui Liu, Donglei Li, Weihao Fu, Xiao Liang, Youguang Li, Yuhang Shi, Wensong Chen, Xiaofang Zhao, Song Medicine (Baltimore) 5700 BACKGROUND: Previous studies investigating the association between BRAF mutations and nonsmall cell lung cancer (NSCLC) remain controversial. To address the issue, we performed an updated meta-analysis of related articles. METHODS: We conducted a comprehensive literature search in the electronic databases including ISI Science Citation Index, EMBASE, PubMed, and CNKI (up to January 2016). The odds ratios (ORs) and 95% confidence interval (CI) were assessed based on random-effects or fixed-effects models according to the heterogeneity of eligible studies. RESULTS: A total of 16 studies enrolled 11,711 patients with NSCLC were involved in the meta-analysis. The overall BRAF mutation rate was 2.6% (303/11,711). There was a significant association between BRAF mutations and adenocarcinomas (ADCs) in NSCLC compared with non-ADCs (OR = 3.96, 95% CI = 2.13–7.34, P < 0.0001). No significant difference was observed in smoking and stage in patients with BRAF mutations. However, a significant difference of BRAF mutation rate was observed between women and men (OR = 0.72, 95% CI = 0.55–0.95, P = 0.02). In addition, the BRAF(V600E) mutations were more frequent in women (OR = 0.45, 95% CI = 0.26–0.77, P = 0.004) and never smokers (OR = 0.12, 95% CI = 0.05–0.29, P < 0.00001). CONCLUSIONS: BRAF mutations in ADCS and female significantly increased the risk of NSCLC compared to non-ADCS and male, respectively. BRAFV(600E) mutation in NSCLC patients was significantly associated with female and nonsmokers. Wolters Kluwer Health 2017-04-07 /pmc/articles/PMC5411210/ /pubmed/28383426 http://dx.doi.org/10.1097/MD.0000000000006552 Text en Copyright © 2017 the Author(s). Published by Wolters Kluwer Health, Inc. http://creativecommons.org/licenses/by-nc/4.0 This is an open access article distributed under the terms of the Creative Commons Attribution-Non Commercial License 4.0 (CCBY-NC), where it is permissible to download, share, remix, transform, and buildup the work provided it is properly cited. The work cannot be used commercially without permission from the journal. http://creativecommons.org/licenses/by-nc/4.0 |
spellingShingle | 5700 Cui, Guanghui Liu, Donglei Li, Weihao Fu, Xiao Liang, Youguang Li, Yuhang Shi, Wensong Chen, Xiaofang Zhao, Song A meta-analysis of the association between BRAF mutation and nonsmall cell lung cancer |
title | A meta-analysis of the association between BRAF mutation and nonsmall cell lung cancer |
title_full | A meta-analysis of the association between BRAF mutation and nonsmall cell lung cancer |
title_fullStr | A meta-analysis of the association between BRAF mutation and nonsmall cell lung cancer |
title_full_unstemmed | A meta-analysis of the association between BRAF mutation and nonsmall cell lung cancer |
title_short | A meta-analysis of the association between BRAF mutation and nonsmall cell lung cancer |
title_sort | meta-analysis of the association between braf mutation and nonsmall cell lung cancer |
topic | 5700 |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5411210/ https://www.ncbi.nlm.nih.gov/pubmed/28383426 http://dx.doi.org/10.1097/MD.0000000000006552 |
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