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The combination of afatinib and bevacizumab in untreated EGFR-mutated advanced lung adenocarcinoma: A multicenter observational study

  • Ping Chih Hsu
  • , Chun Yao Huang
  • , Chin Chou Wang
  • , Scott Chih Hsi Kuo
  • , Chia Hsun Chu
  • , Pi Hung Tung
  • , Allen Chung Cheng Huang
  • , Chih Liang Wang
  • , Li-Chung Chiu
  • , Yueh Fu Fang
  • , Cheng Ta Yang*
  • *此作品的通信作者
  • Chang Gung Memorial Hospital
  • Buddhist Tzu-Chi General Hospital Taiwan
  • Chang Gung University

研究成果: 期刊稿件文章同行評審

17 引文 斯高帕斯(Scopus)

摘要

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.

原文英語
文章編號331
頁(從 - 到)1-12
頁數12
期刊Pharmaceuticals
13
發行號11
DOIs
出版狀態已出版 - 11 2020
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© 2020 by the authors. Licensee MDPI, Basel, Switzerland.

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