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Efficacy and safety of bevacizumab combined with EGFR‐TKIs in advanced non‐small cell lung cancer: A meta‐analysis

BACKGROUND: The aim of this study was to estimate the efficacy and safety of bevacizumab combined with epidermal growth factor receptor tyrosine kinase inhibitors (EGFR TKIs) in advanced non‐small cell lung cancer (NSCLC) patients. METHODS: We searched randomized controlled trials (RCTs) on bevacizu...

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Autores principales: Yang, Yifan, Wang, Liming, Li, Xu, Zhang, Shuai, Yu, Jiangyong, Nie, Xin, Liu, Wenbo, Wu, Xiaonan, Zhang, Ping, Li, Yi, Li, Ailing, Ai, Bin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons Australia, Ltd 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8720617/
https://www.ncbi.nlm.nih.gov/pubmed/34859599
http://dx.doi.org/10.1111/1759-7714.14214
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author Yang, Yifan
Wang, Liming
Li, Xu
Zhang, Shuai
Yu, Jiangyong
Nie, Xin
Liu, Wenbo
Wu, Xiaonan
Zhang, Ping
Li, Yi
Li, Ailing
Ai, Bin
author_facet Yang, Yifan
Wang, Liming
Li, Xu
Zhang, Shuai
Yu, Jiangyong
Nie, Xin
Liu, Wenbo
Wu, Xiaonan
Zhang, Ping
Li, Yi
Li, Ailing
Ai, Bin
author_sort Yang, Yifan
collection PubMed
description BACKGROUND: The aim of this study was to estimate the efficacy and safety of bevacizumab combined with epidermal growth factor receptor tyrosine kinase inhibitors (EGFR TKIs) in advanced non‐small cell lung cancer (NSCLC) patients. METHODS: We searched randomized controlled trials (RCTs) on bevacizumab combined with EGFR TKIs in the NSCLC Cochrane Library, Web of Science, PubMed and Embase. The data were extracted and assessed according to the Cochrane Handbook. We calculated the hazard ratio (HR), risk ratio (RR), and confidence interval (CI), and accomplished this meta‐analysis with Stata 14 software. RESULTS: Of 1301 articles scanned, five articles were involved in this meta‐analysis. We determined that compared with using EGFR TKIs alone, combination treatment significantly prolongs progression‐free survival (PFS) (HR = 0.61, 95% CI = 0.52–0.70; p < 0.001), and increases the objective response rate (ORR) (RR = 1.15, 95% CI: 1.01–1.30, p = 0.10). However, there was no significant difference in overall survival (OS) between the two groups (HR = 0.95, 95% CI = 0.78–1.11; p = <0.001) and combination treatment increases the risks of serious adverse events (SAEs) (RR = 1.58, 95% CI: 1.21–2.05, p = 0.002). CONCLUSIONS: Bevacizumab combined with EGFR‐TKI significantly improves PFS and ORR in patients with advanced NSCLC, but there is no substantial difference in OS and increase the risks of serious adverse events.
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spelling pubmed-87206172022-01-07 Efficacy and safety of bevacizumab combined with EGFR‐TKIs in advanced non‐small cell lung cancer: A meta‐analysis Yang, Yifan Wang, Liming Li, Xu Zhang, Shuai Yu, Jiangyong Nie, Xin Liu, Wenbo Wu, Xiaonan Zhang, Ping Li, Yi Li, Ailing Ai, Bin Thorac Cancer Original Articles BACKGROUND: The aim of this study was to estimate the efficacy and safety of bevacizumab combined with epidermal growth factor receptor tyrosine kinase inhibitors (EGFR TKIs) in advanced non‐small cell lung cancer (NSCLC) patients. METHODS: We searched randomized controlled trials (RCTs) on bevacizumab combined with EGFR TKIs in the NSCLC Cochrane Library, Web of Science, PubMed and Embase. The data were extracted and assessed according to the Cochrane Handbook. We calculated the hazard ratio (HR), risk ratio (RR), and confidence interval (CI), and accomplished this meta‐analysis with Stata 14 software. RESULTS: Of 1301 articles scanned, five articles were involved in this meta‐analysis. We determined that compared with using EGFR TKIs alone, combination treatment significantly prolongs progression‐free survival (PFS) (HR = 0.61, 95% CI = 0.52–0.70; p < 0.001), and increases the objective response rate (ORR) (RR = 1.15, 95% CI: 1.01–1.30, p = 0.10). However, there was no significant difference in overall survival (OS) between the two groups (HR = 0.95, 95% CI = 0.78–1.11; p = <0.001) and combination treatment increases the risks of serious adverse events (SAEs) (RR = 1.58, 95% CI: 1.21–2.05, p = 0.002). CONCLUSIONS: Bevacizumab combined with EGFR‐TKI significantly improves PFS and ORR in patients with advanced NSCLC, but there is no substantial difference in OS and increase the risks of serious adverse events. John Wiley & Sons Australia, Ltd 2021-12-03 2022-01 /pmc/articles/PMC8720617/ /pubmed/34859599 http://dx.doi.org/10.1111/1759-7714.14214 Text en © 2021 The Authors. Thoracic Cancer published by China Lung Oncology Group and John Wiley & Sons Australia, Ltd. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Original Articles
Yang, Yifan
Wang, Liming
Li, Xu
Zhang, Shuai
Yu, Jiangyong
Nie, Xin
Liu, Wenbo
Wu, Xiaonan
Zhang, Ping
Li, Yi
Li, Ailing
Ai, Bin
Efficacy and safety of bevacizumab combined with EGFR‐TKIs in advanced non‐small cell lung cancer: A meta‐analysis
title Efficacy and safety of bevacizumab combined with EGFR‐TKIs in advanced non‐small cell lung cancer: A meta‐analysis
title_full Efficacy and safety of bevacizumab combined with EGFR‐TKIs in advanced non‐small cell lung cancer: A meta‐analysis
title_fullStr Efficacy and safety of bevacizumab combined with EGFR‐TKIs in advanced non‐small cell lung cancer: A meta‐analysis
title_full_unstemmed Efficacy and safety of bevacizumab combined with EGFR‐TKIs in advanced non‐small cell lung cancer: A meta‐analysis
title_short Efficacy and safety of bevacizumab combined with EGFR‐TKIs in advanced non‐small cell lung cancer: A meta‐analysis
title_sort efficacy and safety of bevacizumab combined with egfr‐tkis in advanced non‐small cell lung cancer: a meta‐analysis
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8720617/
https://www.ncbi.nlm.nih.gov/pubmed/34859599
http://dx.doi.org/10.1111/1759-7714.14214
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