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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...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
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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. |
format | Online Article Text |
id | pubmed-7690705 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
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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