Shen Chan, Kehl Kenneth L, Zhao Bo, Simon George R, Zhou Shouhao, Giordano Sharon H
Department of Health Services Research, The University of Texas MD Anderson Cancer Center, Houston, TX; Department of Biostatistics, The University of Texas MD Anderson Cancer Center, Houston, TX.
Division of Cancer Medicine, The University of Texas MD Anderson Cancer Center, Houston, TX.
Clin Lung Cancer. 2017 Jul;18(4):e233-e241. doi: 10.1016/j.cllc.2016.11.002. Epub 2016 Nov 11.
Epidermal growth factor receptor (EGFR)-targeted therapy significantly improves outcomes among patients with non-small-cell lung cancer (NSCLC) whose tumors harbor sensitizing mutations. Patterns of EGFR testing have not been well-documented. The objective of this population-based study is to assess the testing pattern on a national scale.
Using MarketScan 2012 to 2014 data, we identified 5842 patients newly diagnosed with metastatic lung cancer from January 2013 to June 2014 and assessed their EGFR mutation testing pattern in the 6 months after diagnosis. We further examined the testing rate among patients who received the EGFR inhibitor erlotinib. Because histology information is not available in this database, we also conducted a subgroup analysis of EGFR testing among patients who were treated with bevacizumab or pemetrexed, who are likely to have non-squamous NSCLC. Multivariable logistic regression was performed to ascertain factors associated with EGFR testing.
Of 5842 patients with metastatic lung cancer, 1039 (18%) had claims for EGFR testing within 6 months of diagnosis, and 283 (5%) received erlotinib. The testing rate among patients who received erlotinib was 42%. Within a subgroup of 1685 patients treated with bevacizumab or pemetrexed, 616 (37%) underwent EGFR testing. Multivariable logistic regression showed that younger patients, female patients, patients with fewer comorbidities, and patients living in the West region were more likely to receive EGFR testing.
This population-based study demonstrates low EGFR testing rates among advanced lung cancer patients in 2013 and 2014.
表皮生长因子受体(EGFR)靶向治疗可显著改善肿瘤携带敏感突变的非小细胞肺癌(NSCLC)患者的预后。EGFR检测模式尚未得到充分记录。这项基于人群的研究旨在评估全国范围内的检测模式。
利用2012年至2014年的MarketScan数据,我们识别出2013年1月至2014年6月新诊断为转移性肺癌的5842例患者,并评估他们在诊断后6个月内的EGFR突变检测模式。我们进一步检查了接受EGFR抑制剂厄洛替尼治疗的患者的检测率。由于该数据库中没有组织学信息,我们还对接受贝伐单抗或培美曲塞治疗的患者(可能患有非鳞状NSCLC)进行了EGFR检测的亚组分析。进行多变量逻辑回归以确定与EGFR检测相关的因素。
在5842例转移性肺癌患者中,1039例(18%)在诊断后6个月内有EGFR检测记录,283例(5%)接受了厄洛替尼治疗。接受厄洛替尼治疗的患者的检测率为42%。在1685例接受贝伐单抗或培美曲塞治疗的患者亚组中,616例(37%)进行了EGFR检测。多变量逻辑回归显示,年轻患者、女性患者、合并症较少的患者以及居住在西部地区的患者更有可能接受EGFR检测。
这项基于人群的研究表明,2013年和2014年晚期肺癌患者的EGFR检测率较低。