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The association between fibroblast growth factor receptor 1 gene amplification and lung cancer: a meta-analysis

INTRODUCTION: Identifying target oncogenic alterations in lung cancer represents a major development in disease management. We examined the association of fibroblast growth factor receptor 1 (FGFR1) gene amplification with pathological characteristics and geographic region. MATERIAL AND METHODS: We...

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Autores principales: Miao, Jian-Long, Zhou, Jin-Hua, Cai, Jing-Jing, Liu, Rui-Juan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Termedia Publishing House 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6963147/
https://www.ncbi.nlm.nih.gov/pubmed/32051701
http://dx.doi.org/10.5114/aoms.2020.91284
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author Miao, Jian-Long
Zhou, Jin-Hua
Cai, Jing-Jing
Liu, Rui-Juan
author_facet Miao, Jian-Long
Zhou, Jin-Hua
Cai, Jing-Jing
Liu, Rui-Juan
author_sort Miao, Jian-Long
collection PubMed
description INTRODUCTION: Identifying target oncogenic alterations in lung cancer represents a major development in disease management. We examined the association of fibroblast growth factor receptor 1 (FGFR1) gene amplification with pathological characteristics and geographic region. MATERIAL AND METHODS: We conducted a meta-analysis of studies published between January 2010 and October 2016. Relative risks (RR) and corresponding 95% confidence intervals (CI) were calculated regarding the rate of FGFR1 amplification in different lung cancer types and geographic region. RESULTS: Twenty-three studies (5252 patients) were included. There was heterogeneity between studies. However, in subgroup analyses for squamous cell carcinoma (SCC), small cell lung cancer (SCLC), studies using the same definition of FGFR1 amplification, and those from Australia, no significant heterogeneity was detected. The prevalence of FGFR1 amplification in these studies ranged from 4.9% to 49.2% in non-small cell lung cancer (NSCLC), 5.1% to 41.5% in SCC, 0% to 14.7% in adenocarcinoma, and 0% to 7.8% in SCLC. The prevalence of FGFR1 amplification was significantly higher in SCC than in adenocarcinoma (RR = 5.2) and SCLC (RR = 4.2). The prevalence of FGFR1 amplification ranged from 5.6% to 22.2% in Europe, 4.1% to 18.2% in the United States, 7.8% to 49.2% in Asia, and 14.2% to 18.6% in Australia. The rate of FGFR1 amplification was higher in Asians than in non-Asians (RR = 1.9) in NSCLC. CONCLUSIONS: These results suggest that FGFR1 amplification occurs more frequently in SCC and in Asians. FGFR1 amplification may be a potential new therapeutic target for specific patients and lung cancer subtypes.
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spelling pubmed-69631472020-02-12 The association between fibroblast growth factor receptor 1 gene amplification and lung cancer: a meta-analysis Miao, Jian-Long Zhou, Jin-Hua Cai, Jing-Jing Liu, Rui-Juan Arch Med Sci Systemic analysis/Meta-analysis INTRODUCTION: Identifying target oncogenic alterations in lung cancer represents a major development in disease management. We examined the association of fibroblast growth factor receptor 1 (FGFR1) gene amplification with pathological characteristics and geographic region. MATERIAL AND METHODS: We conducted a meta-analysis of studies published between January 2010 and October 2016. Relative risks (RR) and corresponding 95% confidence intervals (CI) were calculated regarding the rate of FGFR1 amplification in different lung cancer types and geographic region. RESULTS: Twenty-three studies (5252 patients) were included. There was heterogeneity between studies. However, in subgroup analyses for squamous cell carcinoma (SCC), small cell lung cancer (SCLC), studies using the same definition of FGFR1 amplification, and those from Australia, no significant heterogeneity was detected. The prevalence of FGFR1 amplification in these studies ranged from 4.9% to 49.2% in non-small cell lung cancer (NSCLC), 5.1% to 41.5% in SCC, 0% to 14.7% in adenocarcinoma, and 0% to 7.8% in SCLC. The prevalence of FGFR1 amplification was significantly higher in SCC than in adenocarcinoma (RR = 5.2) and SCLC (RR = 4.2). The prevalence of FGFR1 amplification ranged from 5.6% to 22.2% in Europe, 4.1% to 18.2% in the United States, 7.8% to 49.2% in Asia, and 14.2% to 18.6% in Australia. The rate of FGFR1 amplification was higher in Asians than in non-Asians (RR = 1.9) in NSCLC. CONCLUSIONS: These results suggest that FGFR1 amplification occurs more frequently in SCC and in Asians. FGFR1 amplification may be a potential new therapeutic target for specific patients and lung cancer subtypes. Termedia Publishing House 2019-12-31 /pmc/articles/PMC6963147/ /pubmed/32051701 http://dx.doi.org/10.5114/aoms.2020.91284 Text en Copyright: © 2019 Termedia & Banach http://creativecommons.org/licenses/by-nc-sa/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0) License, allowing third parties to copy and redistribute the material in any medium or format and to remix, transform, and build upon the material, provided the original work is properly cited and states its license.
spellingShingle Systemic analysis/Meta-analysis
Miao, Jian-Long
Zhou, Jin-Hua
Cai, Jing-Jing
Liu, Rui-Juan
The association between fibroblast growth factor receptor 1 gene amplification and lung cancer: a meta-analysis
title The association between fibroblast growth factor receptor 1 gene amplification and lung cancer: a meta-analysis
title_full The association between fibroblast growth factor receptor 1 gene amplification and lung cancer: a meta-analysis
title_fullStr The association between fibroblast growth factor receptor 1 gene amplification and lung cancer: a meta-analysis
title_full_unstemmed The association between fibroblast growth factor receptor 1 gene amplification and lung cancer: a meta-analysis
title_short The association between fibroblast growth factor receptor 1 gene amplification and lung cancer: a meta-analysis
title_sort association between fibroblast growth factor receptor 1 gene amplification and lung cancer: a meta-analysis
topic Systemic analysis/Meta-analysis
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6963147/
https://www.ncbi.nlm.nih.gov/pubmed/32051701
http://dx.doi.org/10.5114/aoms.2020.91284
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