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首页> 外文期刊>Clinical lung cancer >Epidermal Growth Factor Receptor Mutational Testing and Erlotinib Treatment Among Veterans Diagnosed With Lung Cancer in the United States Department of Veterans Affairs
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Epidermal Growth Factor Receptor Mutational Testing and Erlotinib Treatment Among Veterans Diagnosed With Lung Cancer in the United States Department of Veterans Affairs

机译:表皮生长因子受体突变试验和欧洛替尼在美国退伍军人事务部诊断肺癌患者中的病人治疗

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Micro-Abstract We examined epidermal growth factor receptor gene ( EGFR ) testing and erlotinib treatment among veterans with non–small-cell lung cancer. Veterans had a low (7%) prevalence of EGFR mutations. There were several patients where EGFR testing and erlotinib treatment departed from clinical practice guidelines. Integration of decision support tools into the electronic health record could improve the quality of cancer care. Abstract Introduction We examined mutational testing of the epidermal growth factor gene ( EGFR ) and erlotinib treatment among veterans diagnosed with non–small-cell lung cancer in the United States Department of Veterans Affairs (VA). Our objectives were to identify the prevalence of clinically actionable EGFR mutations, to determine whether testing and treatment were guideline concordant, to evaluate the impact of testing and treatment on survival, and to estimate the rate of testing. Patients and Methods Test results were linked to electronic health records from VA Corporate Data Warehouse and the VA Central Cancer Registry. We analyzed patient demographic and clinical characteristics, prevalence of EGFR mutations, and timing of EGFR mutational testing and erlotinib treatment based on pharmacy records. Overall survival was assessed by Kaplan-Meier analysis. Results Among 973 patients tested at 70 VA medical centers between 2011 and 2013, 64 (7%) had sensitizing EGFR mutations, 694 (71%) were EGFR wild type, and 168 (17%) had clinically insignificant polymorphisms or variants of unknown significance. Results were not documented in 47 tests (5%). Erlotinib administration was in agreement with test results in 843 cases (87%). Conclusion Veterans have a much lower rate of sensitizing EGFR mutations than the reported average of 10% to 15%, which correlates with a high rate of smoking among veterans. This may partially explain clinicians' reluctance to prescribe EGFR testing, which results in underutilization. Although test results appear to have influenced erlotinib treatment decisions, we documented a substantial number of cases where treatment was not applied in accordance with clinical guidelines, potentially resulting in worse outcomes and unnecessary cost.
机译:微摘要我们检查了具有非小细胞肺癌的退伍军人的表皮生长因子受体基因(EGFR)检测和欧洛替尼治疗。退伍军人的EGFR突变具有较低(7%)患病率。有几个患者,EGFR测试和欧尔替尼治疗偏离临床实践指南。将决策支持工具集成到电子健康记录中可以提高癌症护理的质量。摘要介绍,我们检查了在美国退伍军人事务部(VA)中诊断出非小细胞肺癌的退伍军人的表皮生长因子基因(EGFR)和厄洛替尼治疗的突变检测。我们的目标是确定临床可行的EGFR突变的患病率,以确定测试和治疗是否是指南协调,评估测试和治疗对生存的影响,并估算测试率。患者和方法测试结果与VA公司数据仓库和VA中央癌症登记处的电子健康记录相关联。我们分析了患者人口统计和临床特征,EGFR突变的患病率,以及基于药房记录的EGFR突变试验和ERLOTINIB治疗的时间。 Kaplan-Meier分析评估了整体生存率。结果在2011年和2013年的70 VA医疗中心测试的973名患者中,64(7%)致敏EGFR突变,694(71%)是EGFR野生型,168(17%)患有临床微不足道的多态性或不明显的意义的变异性。结果未记录47个测试(5%)。欧洲毒素施用符合843例(87%)的试验结果。结论退伍军人比报告的平均值为10%至15%,退伍军人的敏感性较低,与退伍军人之间的吸烟率很高。这可能部分解释临床医生的不愿意进行公正测试,这导致未充分利用。虽然测试结果似乎受到欧尔替尼治疗决策的影响,但我们记录了大量的病例,其中不按照临床准则申请治疗,可能导致更糟糕的结果和不必要的成本。

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