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Gefitinib provides similar effectiveness and improved safety than erlotinib for advanced non-small cell lung cancer: A meta-analysis

BACKGROUND: The epidermal growth factor receptor tyrosine kinase inhibitors gefitinib and erlotinib are effective for advanced non-small cell lung cancer (NSCLC). This meta-analysis compared their effectiveness and safety. METHODS: We searched systematically in PubMed, ScienceDirect, The Cochrane Li...

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Autores principales: Zhang, Wenxiong, Wei, Yiping, Yu, Dongliang, Xu, Jianjun, Peng, Jinhua
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5916648/
https://www.ncbi.nlm.nih.gov/pubmed/29668619
http://dx.doi.org/10.1097/MD.0000000000010460
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author Zhang, Wenxiong
Wei, Yiping
Yu, Dongliang
Xu, Jianjun
Peng, Jinhua
author_facet Zhang, Wenxiong
Wei, Yiping
Yu, Dongliang
Xu, Jianjun
Peng, Jinhua
author_sort Zhang, Wenxiong
collection PubMed
description BACKGROUND: The epidermal growth factor receptor tyrosine kinase inhibitors gefitinib and erlotinib are effective for advanced non-small cell lung cancer (NSCLC). This meta-analysis compared their effectiveness and safety. METHODS: We searched systematically in PubMed, ScienceDirect, The Cochrane Library, Scopus, Ovid MEDLINE, EMBASE, Web of Science, and Google Scholar for relevant clinical trials regarding gefitinib versus erlotinib for NSCLC. Antitumor effectiveness (overall survival [OS], progression-free survival [PFS], objective response rate [ORR] and disease control rate [DCR]) and adverse effects [AEs]) were assessed. RESULTS: Forty studies comprising 9376 participants were included. The results suggested that gefitinib and erlotinib are effective for advanced NSCLC with comparable PFS (95% confidence intervals [CI]: 0.98–1.11, P = .15), OS (95% CI: 0.93–1.19, P = .45), ORR (95% CI: 0.99–1.16, P = .07), and DCR (95% CI: 0.92–1.03, P = .35). For erlotinib, dose reduction was significantly more frequent (95% CI: 0.10–0.57, P = .001) as were grade 3 to 5 AEs (95% CI: 0.36–0.79, P = .002). In the subgroup analysis, the erlotinib group had a significant higher rate and severity of skin rash, nausea/vomiting, fatigue, and stomatitis. CONCLUSIONS: Gefitinib was proven to be the better choice for advanced NSCLC, with equal antitumor effectiveness and fewer AEs compared with erlotinib. Further large-scale, well-designed randomized controlled trials are warranted to confirm our validation.
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spelling pubmed-59166482018-05-01 Gefitinib provides similar effectiveness and improved safety than erlotinib for advanced non-small cell lung cancer: A meta-analysis Zhang, Wenxiong Wei, Yiping Yu, Dongliang Xu, Jianjun Peng, Jinhua Medicine (Baltimore) 5700 BACKGROUND: The epidermal growth factor receptor tyrosine kinase inhibitors gefitinib and erlotinib are effective for advanced non-small cell lung cancer (NSCLC). This meta-analysis compared their effectiveness and safety. METHODS: We searched systematically in PubMed, ScienceDirect, The Cochrane Library, Scopus, Ovid MEDLINE, EMBASE, Web of Science, and Google Scholar for relevant clinical trials regarding gefitinib versus erlotinib for NSCLC. Antitumor effectiveness (overall survival [OS], progression-free survival [PFS], objective response rate [ORR] and disease control rate [DCR]) and adverse effects [AEs]) were assessed. RESULTS: Forty studies comprising 9376 participants were included. The results suggested that gefitinib and erlotinib are effective for advanced NSCLC with comparable PFS (95% confidence intervals [CI]: 0.98–1.11, P = .15), OS (95% CI: 0.93–1.19, P = .45), ORR (95% CI: 0.99–1.16, P = .07), and DCR (95% CI: 0.92–1.03, P = .35). For erlotinib, dose reduction was significantly more frequent (95% CI: 0.10–0.57, P = .001) as were grade 3 to 5 AEs (95% CI: 0.36–0.79, P = .002). In the subgroup analysis, the erlotinib group had a significant higher rate and severity of skin rash, nausea/vomiting, fatigue, and stomatitis. CONCLUSIONS: Gefitinib was proven to be the better choice for advanced NSCLC, with equal antitumor effectiveness and fewer AEs compared with erlotinib. Further large-scale, well-designed randomized controlled trials are warranted to confirm our validation. Wolters Kluwer Health 2018-04-20 /pmc/articles/PMC5916648/ /pubmed/29668619 http://dx.doi.org/10.1097/MD.0000000000010460 Text en Copyright © 2018 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
Zhang, Wenxiong
Wei, Yiping
Yu, Dongliang
Xu, Jianjun
Peng, Jinhua
Gefitinib provides similar effectiveness and improved safety than erlotinib for advanced non-small cell lung cancer: A meta-analysis
title Gefitinib provides similar effectiveness and improved safety than erlotinib for advanced non-small cell lung cancer: A meta-analysis
title_full Gefitinib provides similar effectiveness and improved safety than erlotinib for advanced non-small cell lung cancer: A meta-analysis
title_fullStr Gefitinib provides similar effectiveness and improved safety than erlotinib for advanced non-small cell lung cancer: A meta-analysis
title_full_unstemmed Gefitinib provides similar effectiveness and improved safety than erlotinib for advanced non-small cell lung cancer: A meta-analysis
title_short Gefitinib provides similar effectiveness and improved safety than erlotinib for advanced non-small cell lung cancer: A meta-analysis
title_sort gefitinib provides similar effectiveness and improved safety than erlotinib for advanced non-small cell lung cancer: a meta-analysis
topic 5700
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5916648/
https://www.ncbi.nlm.nih.gov/pubmed/29668619
http://dx.doi.org/10.1097/MD.0000000000010460
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