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未经治疗的转移性表皮生长因子受体(EGFR)突变型肺腺癌患者接受一线厄洛替尼和贝伐单抗联合治疗的真实世界分析

A Real-World Analysis of Patients with Untreated Metastatic Epidermal Growth Factor Receptor (EGFR)-Mutated Lung Adenocarcinoma Receiving First-Line Erlotinib and Bevacizumab Combination Therapy.

作者信息

Wang Chin-Chou, Chiu Li-Chung, Tung Pi-Hung, Kuo Scott Chih-Hsi, Chu Chia-Hsun, Huang Allen Chung-Cheng, Wang Chih-Liang, Chen Chih-Hung, Yang Cheng-Ta, Hsu Ping-Chih

机构信息

Division of Pulmonary and Critical Care Medicine, Kaohsiung Chang Gung Memorial Hospital, Kaohsiung City, 83301, Taiwan.

Department of Thoracic Medicine, Chang Gung Memorial Hospital at Linkou, No. 5, Fuxing 1st Rd., Guishan Dist., Taoyuan City, 333005, Taiwan.

出版信息

Oncol Ther. 2021 Dec;9(2):489-503. doi: 10.1007/s40487-021-00152-6. Epub 2021 May 15.

DOI:10.1007/s40487-021-00152-6
PMID:33990928
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8593121/
Abstract

INTRODUCTION

The clinical features of patients with metastatic epidermal growth factor receptor (EGFR)-mutated lung adenocarcinoma receiving first-line therapy based on erlotinib combined with bevacizumab are unclear. Here, we sought to analyze the clinical features of this patient group.

METHODS

Data were analyzed for the period from January 2015 to August 2019 for 49 patients with metastatic EGFR-mutated lung adenocarcinoma receiving first-line erlotinib-and-bevacizumab combination therapy from the Linkou and Kaohsiung Chang Gung Memorial Hospitals.

RESULTS

The combination of erlotinib and bevacizumab showed an 83.7% objective response rate and a 97.9% disease control rate. The median progression-free survival (PFS) and overall survival (OS) were 22.0 [95% CI (19.7-22.33)] and 47.6 [95% CI (38.87-56.37)] months, respectively, for all patients. The secondary EGFR-T790M mutation rate in the patients with acquired resistance to the combination was 72.4%. No predictive factor associated with the appearance of secondary EGFR-T790M mutations was found. The most frequent adverse event (AE) caused by the combination therapy was dermatitis (100%), and most of the AEs were manageable and grades 1 and 2.

CONCLUSION

Erlotinib combined with bevacizumab is an effective and safe therapy for untreated metastatic EGFR-mutated lung adenocarcinoma. The combination does not alter secondary EGFR-T790M mutations in patients with acquired resistance and is feasible in real-world clinical practice.

摘要

引言

接受基于厄洛替尼联合贝伐单抗的一线治疗的转移性表皮生长因子受体(EGFR)突变肺腺癌患者的临床特征尚不清楚。在此,我们试图分析该患者群体的临床特征。

方法

分析了2015年1月至2019年8月期间,来自林口长庚纪念医院和高雄长庚纪念医院的49例接受一线厄洛替尼联合贝伐单抗治疗的转移性EGFR突变肺腺癌患者的数据。

结果

厄洛替尼与贝伐单抗联合使用的客观缓解率为83.7%,疾病控制率为97.9%。所有患者的中位无进展生存期(PFS)和总生存期(OS)分别为22.0[95%置信区间(19.7 - 22.33)]个月和47.6[95%置信区间(38.87 - 56.37)]个月。联合治疗获得性耐药患者的继发性EGFR-T790M突变率为72.4%。未发现与继发性EGFR-T790M突变出现相关的预测因素。联合治疗引起的最常见不良事件(AE)是皮炎(100%),且大多数AE可控制,为1级和2级。

结论

厄洛替尼联合贝伐单抗是未经治疗的转移性EGFR突变肺腺癌的一种有效且安全的治疗方法。该联合方案不会改变获得性耐药患者的继发性EGFR-T790M突变,在现实世界临床实践中是可行的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/232c/8593121/1489478fd0db/40487_2021_152_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/232c/8593121/622863ec29a4/40487_2021_152_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/232c/8593121/73e31de0de7f/40487_2021_152_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/232c/8593121/1489478fd0db/40487_2021_152_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/232c/8593121/622863ec29a4/40487_2021_152_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/232c/8593121/73e31de0de7f/40487_2021_152_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/232c/8593121/1489478fd0db/40487_2021_152_Fig3_HTML.jpg

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