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Epidermal growth factor receptor is associated with the onset of skeletal related events in non-small cell lung cancer

BACKGROUND: Bone metastasis and skeletal related events (SREs) are common in non-small cell lung cancer (NSCLC). Patients with mutant epidermal growth factor receptor (EGFR) could benefit from tyrosine kinase inhibitors (TKIs). However, it is unclear whether SRE is influenced by EGFR status. We aime...

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Autores principales: Huang, Shu-Mei, Yang, Jin-Ji, Chen, Hua-Jun, Wu, Si-Pei, Bai, Xiao-Yan, Zhou, Qing, Tu, Hai-Yan, Wu, Yi-Long
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5655291/
https://www.ncbi.nlm.nih.gov/pubmed/29113396
http://dx.doi.org/10.18632/oncotarget.18759
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author Huang, Shu-Mei
Yang, Jin-Ji
Chen, Hua-Jun
Wu, Si-Pei
Bai, Xiao-Yan
Zhou, Qing
Tu, Hai-Yan
Wu, Yi-Long
author_facet Huang, Shu-Mei
Yang, Jin-Ji
Chen, Hua-Jun
Wu, Si-Pei
Bai, Xiao-Yan
Zhou, Qing
Tu, Hai-Yan
Wu, Yi-Long
author_sort Huang, Shu-Mei
collection PubMed
description BACKGROUND: Bone metastasis and skeletal related events (SREs) are common in non-small cell lung cancer (NSCLC). Patients with mutant epidermal growth factor receptor (EGFR) could benefit from tyrosine kinase inhibitors (TKIs). However, it is unclear whether SRE is influenced by EGFR status. We aimed to evaluate the correlation of EGFR status and TKIs with the incidence of SREs. METHODS: We conducted a retrospective study of stage IV NSCLC patients with bone metastasis. Incidence rate of SREs was collected and was compared using chi-square test. Logistic-regression analysis was used to identify the risk factors predicting the incidence of SREs. RESULTS: 410 eligible patients were enrolled in the study. 49.0% were detected with EGFR mutation. 49.8% of patients received EGFR-TKIs therapy prior to the onset of SREs. 42.7% experienced at least one SRE. Patients who were treated with TKIs held lower incidence of SREs than patients who were not treated with TKIs (23.5% vs 61.7%, p<0.001). Multivariate analysis showed that poor performance status (OR 5.550, 95%CI 2.290-13.450; p<0.001) and mutant EGFR (OR 3.050, 95%CI 1.608-5.787, p=0.001) were independent risk factors predicting the onset of SREs, while the usage of TKIs (OR 0.102, 95%CI 0.054-0.193, p<0.001) was a protective factor of SREs in NSCLC patients with bone metastasis. CONCLUSIONS: This study indicates that the incidence of SREs is common in both patients with and without EGFR mutation. Poor performance ability and mutant EGFR imply higher risks of SREs, while the usage of TKIs may be a protective factor of SREs.
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spelling pubmed-56552912017-11-06 Epidermal growth factor receptor is associated with the onset of skeletal related events in non-small cell lung cancer Huang, Shu-Mei Yang, Jin-Ji Chen, Hua-Jun Wu, Si-Pei Bai, Xiao-Yan Zhou, Qing Tu, Hai-Yan Wu, Yi-Long Oncotarget Clinical Research Paper BACKGROUND: Bone metastasis and skeletal related events (SREs) are common in non-small cell lung cancer (NSCLC). Patients with mutant epidermal growth factor receptor (EGFR) could benefit from tyrosine kinase inhibitors (TKIs). However, it is unclear whether SRE is influenced by EGFR status. We aimed to evaluate the correlation of EGFR status and TKIs with the incidence of SREs. METHODS: We conducted a retrospective study of stage IV NSCLC patients with bone metastasis. Incidence rate of SREs was collected and was compared using chi-square test. Logistic-regression analysis was used to identify the risk factors predicting the incidence of SREs. RESULTS: 410 eligible patients were enrolled in the study. 49.0% were detected with EGFR mutation. 49.8% of patients received EGFR-TKIs therapy prior to the onset of SREs. 42.7% experienced at least one SRE. Patients who were treated with TKIs held lower incidence of SREs than patients who were not treated with TKIs (23.5% vs 61.7%, p<0.001). Multivariate analysis showed that poor performance status (OR 5.550, 95%CI 2.290-13.450; p<0.001) and mutant EGFR (OR 3.050, 95%CI 1.608-5.787, p=0.001) were independent risk factors predicting the onset of SREs, while the usage of TKIs (OR 0.102, 95%CI 0.054-0.193, p<0.001) was a protective factor of SREs in NSCLC patients with bone metastasis. CONCLUSIONS: This study indicates that the incidence of SREs is common in both patients with and without EGFR mutation. Poor performance ability and mutant EGFR imply higher risks of SREs, while the usage of TKIs may be a protective factor of SREs. Impact Journals LLC 2017-06-28 /pmc/articles/PMC5655291/ /pubmed/29113396 http://dx.doi.org/10.18632/oncotarget.18759 Text en Copyright: © 2017 Huang et al. http://creativecommons.org/licenses/by/3.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/) (CC-BY), which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Clinical Research Paper
Huang, Shu-Mei
Yang, Jin-Ji
Chen, Hua-Jun
Wu, Si-Pei
Bai, Xiao-Yan
Zhou, Qing
Tu, Hai-Yan
Wu, Yi-Long
Epidermal growth factor receptor is associated with the onset of skeletal related events in non-small cell lung cancer
title Epidermal growth factor receptor is associated with the onset of skeletal related events in non-small cell lung cancer
title_full Epidermal growth factor receptor is associated with the onset of skeletal related events in non-small cell lung cancer
title_fullStr Epidermal growth factor receptor is associated with the onset of skeletal related events in non-small cell lung cancer
title_full_unstemmed Epidermal growth factor receptor is associated with the onset of skeletal related events in non-small cell lung cancer
title_short Epidermal growth factor receptor is associated with the onset of skeletal related events in non-small cell lung cancer
title_sort epidermal growth factor receptor is associated with the onset of skeletal related events in non-small cell lung cancer
topic Clinical Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5655291/
https://www.ncbi.nlm.nih.gov/pubmed/29113396
http://dx.doi.org/10.18632/oncotarget.18759
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