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美国晚期非小细胞肺癌患者的真实世界生物标志物检测与总生存期趋势。

Trends in real-world biomarker testing and overall survival in US patients with advanced non-small-cell lung cancer.

机构信息

Regeneron Pharmaceuticals, Inc., 777 Old Saw Mill River Rd, Tarrytown, NY 10591, USA.

Genesis Research, LLC, 111 River Street, Suite 1120, Hoboken, NJ 07030, USA.

出版信息

Future Oncol. 2022 Dec;18(39):4385-4397. doi: 10.2217/fon-2022-0540. Epub 2023 Jan 19.

Abstract

Trends/outcomes associated with National Comprehensive Cancer Network (NCCN)-recommended biomarker testing to guide advanced non-small-cell lung cancer (aNSCLC) treatment were assessed. Patients initiating first-line aNSCLC treatment were included using a nationwide electronic health record-derived database (1/1/2015-10/31/2021). Trends in pre-first-line biomarker testing (PD-L1, major genomic aberrations), factors associated with testing and associations between testing and outcomes were assessed. PD-L1/genomic aberration testing rates increased from 33% (2016) to 81% (2018), then plateaued. Certain clinical and demographic factors were associated with a greater likelihood of PD-L1 testing. Patients tested for PD-L1 or genomic aberrations had longer overall survival (OS). Biomarker testing may be associated with improved OS in aNSCLC, though not all patients had equal access to testing.

摘要

评估了与美国国家综合癌症网络(NCCN)推荐的生物标志物检测相关的趋势/结果,以指导晚期非小细胞肺癌(aNSCLC)的治疗。使用全国范围内的电子健康记录衍生数据库(2015 年 1 月 1 日至 2021 年 10 月 31 日)纳入开始一线 aNSCLC 治疗的患者。评估了一线前生物标志物检测(PD-L1、主要基因组异常)的趋势、与检测相关的因素以及检测与结果之间的关联。PD-L1/基因组异常检测率从 33%(2016 年)增加到 81%(2018 年),然后趋于平稳。某些临床和人口统计学因素与 PD-L1 检测的可能性更大相关。接受 PD-L1 或基因组异常检测的患者总生存期(OS)更长。生物标志物检测可能与 aNSCLC 的 OS 改善相关,但并非所有患者都能平等获得检测。

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