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The Combination of Afatinib and Bevacizumab in Untreated EGFR-Mutated Advanced Lung Adenocarcinoma: A Multicenter Observational Study

The efficacy of afatinib in combination with bevacizumab in untreated advanced epidermal growth factor receptor (EGFR)-mutated lung adenocarcinoma is currently unclear. We sought to investigate the efficacy of this combination through a multicenter observational analysis. Data for 57 patients with a...

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Autores principales: Hsu, Ping-Chih, Huang, Chun-Yao, Wang, Chin-Chou, Kuo, Scott Chih-Hsi, Chu, Chia-Hsun, Tung, Pi-Hung, Huang, Allen Chung-Cheng, Wang, Chih-Liang, Chiu, Li-Chung, Fang, Yueh-Fu, Yang, Cheng-Ta
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7690705/
https://www.ncbi.nlm.nih.gov/pubmed/33113888
http://dx.doi.org/10.3390/ph13110331
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author Hsu, Ping-Chih
Huang, Chun-Yao
Wang, Chin-Chou
Kuo, Scott Chih-Hsi
Chu, Chia-Hsun
Tung, Pi-Hung
Huang, Allen Chung-Cheng
Wang, Chih-Liang
Chiu, Li-Chung
Fang, Yueh-Fu
Yang, Cheng-Ta
author_facet Hsu, Ping-Chih
Huang, Chun-Yao
Wang, Chin-Chou
Kuo, Scott Chih-Hsi
Chu, Chia-Hsun
Tung, Pi-Hung
Huang, Allen Chung-Cheng
Wang, Chih-Liang
Chiu, Li-Chung
Fang, Yueh-Fu
Yang, Cheng-Ta
author_sort Hsu, Ping-Chih
collection PubMed
description The efficacy of afatinib in combination with bevacizumab in untreated advanced epidermal growth factor receptor (EGFR)-mutated lung adenocarcinoma is currently unclear. We sought to investigate the efficacy of this combination through a multicenter observational analysis. Data for 57 patients with advanced EGFR-mutated lung adenocarcinoma who received afatinib combined with bevacizumab as first-line therapy at the Chang Gung Memorial Hospitals in Linkou and Kaohsiung and Taipei Tzu Chi Hospital from May 2015 to July 2019 were analyzed. The objective response rate and disease control rate of afatinib combined with bevacizumab therapy were 87.7% and 100%, respectively. In all patients, the median progression-free survival (PFS) and overall survival (OS) were 23.9 (95% confidence interval (CI) (17.56–29.17)) and 45.9 (95% CI (39.50–53.60)) months, respectively. No statistical significance between exon 19 deletion and L858R mutations was noted in PFS or OS. The most frequent adverse events (AEs) were diarrhea (98.2%) and dermatitis (96.5%), and most AEs were grade 2 or lower and manageable. The combination of afatinib and bevacizumab is an effective therapy for untreated advanced EGFR-mutated lung adenocarcinoma with acceptable safety. Future prospective studies focusing on this combination for untreated advanced EGFR-mutated lung adenocarcinoma are warranted.
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spelling pubmed-76907052020-11-27 The Combination of Afatinib and Bevacizumab in Untreated EGFR-Mutated Advanced Lung Adenocarcinoma: A Multicenter Observational Study Hsu, Ping-Chih Huang, Chun-Yao Wang, Chin-Chou Kuo, Scott Chih-Hsi Chu, Chia-Hsun Tung, Pi-Hung Huang, Allen Chung-Cheng Wang, Chih-Liang Chiu, Li-Chung Fang, Yueh-Fu Yang, Cheng-Ta Pharmaceuticals (Basel) Article The efficacy of afatinib in combination with bevacizumab in untreated advanced epidermal growth factor receptor (EGFR)-mutated lung adenocarcinoma is currently unclear. We sought to investigate the efficacy of this combination through a multicenter observational analysis. Data for 57 patients with advanced EGFR-mutated lung adenocarcinoma who received afatinib combined with bevacizumab as first-line therapy at the Chang Gung Memorial Hospitals in Linkou and Kaohsiung and Taipei Tzu Chi Hospital from May 2015 to July 2019 were analyzed. The objective response rate and disease control rate of afatinib combined with bevacizumab therapy were 87.7% and 100%, respectively. In all patients, the median progression-free survival (PFS) and overall survival (OS) were 23.9 (95% confidence interval (CI) (17.56–29.17)) and 45.9 (95% CI (39.50–53.60)) months, respectively. No statistical significance between exon 19 deletion and L858R mutations was noted in PFS or OS. The most frequent adverse events (AEs) were diarrhea (98.2%) and dermatitis (96.5%), and most AEs were grade 2 or lower and manageable. The combination of afatinib and bevacizumab is an effective therapy for untreated advanced EGFR-mutated lung adenocarcinoma with acceptable safety. Future prospective studies focusing on this combination for untreated advanced EGFR-mutated lung adenocarcinoma are warranted. MDPI 2020-10-23 /pmc/articles/PMC7690705/ /pubmed/33113888 http://dx.doi.org/10.3390/ph13110331 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Hsu, Ping-Chih
Huang, Chun-Yao
Wang, Chin-Chou
Kuo, Scott Chih-Hsi
Chu, Chia-Hsun
Tung, Pi-Hung
Huang, Allen Chung-Cheng
Wang, Chih-Liang
Chiu, Li-Chung
Fang, Yueh-Fu
Yang, Cheng-Ta
The Combination of Afatinib and Bevacizumab in Untreated EGFR-Mutated Advanced Lung Adenocarcinoma: A Multicenter Observational Study
title The Combination of Afatinib and Bevacizumab in Untreated EGFR-Mutated Advanced Lung Adenocarcinoma: A Multicenter Observational Study
title_full The Combination of Afatinib and Bevacizumab in Untreated EGFR-Mutated Advanced Lung Adenocarcinoma: A Multicenter Observational Study
title_fullStr The Combination of Afatinib and Bevacizumab in Untreated EGFR-Mutated Advanced Lung Adenocarcinoma: A Multicenter Observational Study
title_full_unstemmed The Combination of Afatinib and Bevacizumab in Untreated EGFR-Mutated Advanced Lung Adenocarcinoma: A Multicenter Observational Study
title_short The Combination of Afatinib and Bevacizumab in Untreated EGFR-Mutated Advanced Lung Adenocarcinoma: A Multicenter Observational Study
title_sort combination of afatinib and bevacizumab in untreated egfr-mutated advanced lung adenocarcinoma: a multicenter observational study
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7690705/
https://www.ncbi.nlm.nih.gov/pubmed/33113888
http://dx.doi.org/10.3390/ph13110331
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