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논문 기본 정보

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학술저널
저자정보
Yen-Hsiang Huang (Taichung Veterans General Hospital Taichung Taiwan) Kuo-Hsuan Hsu (Taichung Veterans General Hospital Taichung Taiwan) Chun-Shih Chin (Taichung Veterans General Hospital Taichung Taiwan) Jeng-Sen Tseng (Taichung Veterans General Hospital Taichung Taiwan) Tsung-Ying Yang (Taichung Veterans General Hospital Taichung Taiwan) Kun-Chieh Chen (Chung Shan Medical University Hospital, Taichung, Taiwan) Kang-Yi Su (National Taiwan University Hospital Taipei Taiwan) Sung-Liang Yu (National Taiwan University Hospital Taipei Taiwan) Jeremy J.W. Chen (National Chung Hsing University Taichung Taiwan) Gee-Chen Chang (National Chung Hsing University Taichung Taiwan)
저널정보
대한암학회 Cancer Research and Treatment Cancer Research and Treatment 제54권 제2호
발행연도
2022.4
수록면
434 - 444 (11page)
DOI
10.4143/crt.2021.671

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PurposeThe aim of this study was to investigate the efficacy of various epidermal growth factor receptor (EGFR)?tyrosine kinase inhibitors (TKIs) plus bevacizumab in advanced <i>EGFR</i>-mutant lung adenocarcinoma patients.Materials and MethodsFrom August 2016 to October 2020, we enrolled advanced lung adenocarcinoma patients harboring exon 19 deletion or L858R receiving gefitinib, erlotinib and afatinib plus bevacizumab as the first-line treatment for the purposes of analysis.ResultsA total of 36 patients were included in the final analysis. Three patients received gefitinib, 17 received erlotinib, and 16 received afatinib combined with bevacizumab as the first-line treatment. The objective response rate was 77.8%, and disease control rate was 94.4%. The overall median progression-free survival (PFS) was 16.4 months, while the median PFS was 17.1 months in patients with exon 19 deletion, and 16.2 months in patients with L858R mutation (p=0.311). Regarding the use of different EGFR-TKIs, the median PFS was 17.1 months in the erlotinib group and 21.6 months in the afatinib group (p=0.617). In patients with brain metastasis at baseline, the median PFS was 18.9 months in the erlotinib group and 16.4 months in the afatinib group (p=0.747). Amongst patients harboring exon 19 deletion, the median PFS was 16.2 months in the erlotinib group and not-reached in the afatinib group (p=0.141). In patients with L858R mutation, the median PFS was 18.9 months in the erlotinib group and 16.2 months in the afatinib group (p=0.481).ConclusionOur research demonstrates that not only erlotinib combined with bevacizumab, but also afatinib plus bevacizumab as first-line treatment, provides solid clinical efficacy in advanced <i>EGFR</i>-mutant lung adenocarcinoma patients.

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