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The number of brain metastases predicts the survival of non‐small cell lung cancer patients with EGFR mutation status

BACKGROUND: Lung cancer is the common cause of cancer‐related deaths throughout the world, and brain is a frequent metastatic site of lung cancer. AIM: This research sought to evaluate the impact of the number of brain metastases in prognosticating non‐small cell lung cancer (NSCLC) patients account...

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Autores principales: Shao, Jun, Li, Jingwei, Song, Lujia, He, Qiuyao, Wu, Yuxuan, Li, Linhui, Liu, Dan, Wang, Chengdi, Li, Weimin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9458511/
https://www.ncbi.nlm.nih.gov/pubmed/34766737
http://dx.doi.org/10.1002/cnr2.1550
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author Shao, Jun
Li, Jingwei
Song, Lujia
He, Qiuyao
Wu, Yuxuan
Li, Linhui
Liu, Dan
Wang, Chengdi
Li, Weimin
author_facet Shao, Jun
Li, Jingwei
Song, Lujia
He, Qiuyao
Wu, Yuxuan
Li, Linhui
Liu, Dan
Wang, Chengdi
Li, Weimin
author_sort Shao, Jun
collection PubMed
description BACKGROUND: Lung cancer is the common cause of cancer‐related deaths throughout the world, and brain is a frequent metastatic site of lung cancer. AIM: This research sought to evaluate the impact of the number of brain metastases in prognosticating non‐small cell lung cancer (NSCLC) patients accounting to the role of epidermal growth factor receptor (EGFR) mutations. METHODS AND RESULTS: NSCLC patients with brain metastases diagnosed/treated in West China Hospital, Sichuan University between 2009 and 2017 were identified retrospectively. Kaplan–Meier approach was adopted to estimate OS. And we performed univariate and multivariate Cox proportional hazards regression analyses of characteristics related to overall survival (OS) in both EGFR‐mutated and wild‐type cohorts. In total, this study included 611 eligible NSCLC patients with brain metastases. Extracranial metastases and chemotherapy were independent prognostic factors of OS in both cohorts. As the disease progressed, EGFR‐mutated patients had brain metastasis significantly earlier (P < .0001), but they also had notably better survival outcomes than wild‐type patients (P < .0001). And the number of brain metastases impacted the survival incidence in the progression significantly in both EGFR‐mutated and wild‐type groups (P = .0087/.037, respectively). CONCLUSION: The number of brain metastases was a prognostic factor for lung cancer patients either with EGFR mutations or with wild‐type EGFR, with larger number indicating more unfavorble clinical outcomes. Patients with EGFR mutations had a better survival.
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spelling pubmed-94585112022-09-12 The number of brain metastases predicts the survival of non‐small cell lung cancer patients with EGFR mutation status Shao, Jun Li, Jingwei Song, Lujia He, Qiuyao Wu, Yuxuan Li, Linhui Liu, Dan Wang, Chengdi Li, Weimin Cancer Rep (Hoboken) Original Articles BACKGROUND: Lung cancer is the common cause of cancer‐related deaths throughout the world, and brain is a frequent metastatic site of lung cancer. AIM: This research sought to evaluate the impact of the number of brain metastases in prognosticating non‐small cell lung cancer (NSCLC) patients accounting to the role of epidermal growth factor receptor (EGFR) mutations. METHODS AND RESULTS: NSCLC patients with brain metastases diagnosed/treated in West China Hospital, Sichuan University between 2009 and 2017 were identified retrospectively. Kaplan–Meier approach was adopted to estimate OS. And we performed univariate and multivariate Cox proportional hazards regression analyses of characteristics related to overall survival (OS) in both EGFR‐mutated and wild‐type cohorts. In total, this study included 611 eligible NSCLC patients with brain metastases. Extracranial metastases and chemotherapy were independent prognostic factors of OS in both cohorts. As the disease progressed, EGFR‐mutated patients had brain metastasis significantly earlier (P < .0001), but they also had notably better survival outcomes than wild‐type patients (P < .0001). And the number of brain metastases impacted the survival incidence in the progression significantly in both EGFR‐mutated and wild‐type groups (P = .0087/.037, respectively). CONCLUSION: The number of brain metastases was a prognostic factor for lung cancer patients either with EGFR mutations or with wild‐type EGFR, with larger number indicating more unfavorble clinical outcomes. Patients with EGFR mutations had a better survival. John Wiley and Sons Inc. 2021-11-12 /pmc/articles/PMC9458511/ /pubmed/34766737 http://dx.doi.org/10.1002/cnr2.1550 Text en © 2021 The Authors. Cancer Reports published by Wiley Periodicals LLC. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Shao, Jun
Li, Jingwei
Song, Lujia
He, Qiuyao
Wu, Yuxuan
Li, Linhui
Liu, Dan
Wang, Chengdi
Li, Weimin
The number of brain metastases predicts the survival of non‐small cell lung cancer patients with EGFR mutation status
title The number of brain metastases predicts the survival of non‐small cell lung cancer patients with EGFR mutation status
title_full The number of brain metastases predicts the survival of non‐small cell lung cancer patients with EGFR mutation status
title_fullStr The number of brain metastases predicts the survival of non‐small cell lung cancer patients with EGFR mutation status
title_full_unstemmed The number of brain metastases predicts the survival of non‐small cell lung cancer patients with EGFR mutation status
title_short The number of brain metastases predicts the survival of non‐small cell lung cancer patients with EGFR mutation status
title_sort number of brain metastases predicts the survival of non‐small cell lung cancer patients with egfr mutation status
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9458511/
https://www.ncbi.nlm.nih.gov/pubmed/34766737
http://dx.doi.org/10.1002/cnr2.1550
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