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美国非小细胞肺癌患者基于 EGFR 突变状态的治疗模式:一项回顾性数据库分析。

Treatment Patterns by EGFR Mutation Status in Non-Small Cell Lung Cancer Patients in the USA: A Retrospective Database Analysis.

机构信息

McKesson Specialty Health, Woodlands, TX, USA.

Eli Lilly and Company, Lilly Corporate Center, Indianapolis, IN, USA.

出版信息

Adv Ther. 2018 Nov;35(11):1905-1919. doi: 10.1007/s12325-018-0811-0. Epub 2018 Oct 19.

Abstract

INTRODUCTION

Targeted therapies, including tyrosine kinase inhibitors (TKIs) that target the sensitizing epidermal growth factor receptor (EGFR) gene are recommended for patients with non-small cell lung cancer (NSCLC). Most patients with NSCLC who test positive for the EGFR mutation and receive TKIs develop resistance to these drugs. Questions remain regarding which treatment sequence is optimal for patients with EGFR-mutant NSCLC, and few studies have evaluated patterns of TKI treatment use in NSCLC, irrespective of EGFR mutation status, in a real-world setting. This population-based study aimed to evaluate treatment patterns at a national level in the USA.

METHODS

This retrospective observational study used data from the US Oncology Network's iKnowMed database. Patients with advanced NSCLC who initiated first-line therapy with erlotinib and/or intravenous chemotherapy between January 1, 2012 and June 30, 2015 and met all other study criteria were included. Descriptive analyses assessed demographic and clinical characteristics and treatment patterns among the overall study cohort, as well as for specific erlotinib treatment subgroups, stratified by EGFR status.

RESULTS

Among the 3108 patients identified, 18.5% were EGFR positive, 49.8% were EGFR negative, and 31.7% were EGFR documented unknown. For the overall cohort, 18.4% received first-line erlotinib monotherapy, fewer than 1% received first-line combination therapy (erlotinib plus chemotherapy), 4.7% received second-line erlotinib monotherapy, and 3.3% received second-line combination therapy. First-line erlotinib monotherapy was used in 77.8% of all EGFR positive patients. Almost two-thirds of the overall cohort were not observed to have advanced to second-line therapy.

CONCLUSIONS

As treatment options evolve, this study provides real-world treatment patterns that suggest concordance with NCCN guidelines and confirm the remaining need to understand sequencing of therapies and related outcomes.

FUNDING

Eli Lilly and Company.

摘要

简介

针对具有敏感表皮生长因子受体(EGFR)基因突变的非小细胞肺癌(NSCLC)患者,推荐使用靶向治疗,包括针对 EGFR 基因的酪氨酸激酶抑制剂(TKIs)。大多数 EGFR 基因突变阳性并接受 TKI 治疗的 NSCLC 患者会对这些药物产生耐药性。对于 EGFR 突变型 NSCLC 患者,哪种治疗方案最佳仍存在疑问,而且很少有研究在真实环境中评估无论 EGFR 突变状态如何,NSCLC 患者 TKI 治疗的使用模式。本基于人群的研究旨在评估美国全国范围内的治疗模式。

方法

本回顾性观察性研究使用了美国肿瘤学网络的 iKnowMed 数据库的数据。纳入 2012 年 1 月 1 日至 2015 年 6 月 30 日期间接受一线厄洛替尼和/或静脉化疗治疗的晚期 NSCLC 患者,且符合所有其他研究标准。描述性分析评估了总体研究队列的人口统计学和临床特征以及治疗模式,以及根据 EGFR 状态分层的特定厄洛替尼治疗亚组。

结果

在确定的 3108 例患者中,18.5%为 EGFR 阳性,49.8%为 EGFR 阴性,31.7%为 EGFR 记录不详。对于整个队列,18.4%接受一线厄洛替尼单药治疗,不到 1%接受一线联合治疗(厄洛替尼加化疗),4.7%接受二线厄洛替尼单药治疗,3.3%接受二线联合治疗。所有 EGFR 阳性患者中,77.8%接受一线厄洛替尼单药治疗。总体队列中近三分之二的患者未观察到进展至二线治疗。

结论

随着治疗选择的发展,本研究提供了真实世界的治疗模式,表明与 NCCN 指南一致,并证实仍需要了解治疗方案的顺序和相关结果。

资金来源

礼来公司。

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