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EGFR gene-mutation status correlated with therapeutic decision making in lung adenocarcinoma

机译:EGFR基因突变状态与肺腺癌治疗决策相关

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摘要

The purpose of this study was to investigate the correlation between EGFR-mutation status and treatment efficacy for advanced lung adenocarcinoma patients. A total of 47 patients receiving erlotinib as first-line therapy were divided into two groups: the EGFR gene mutation group included 19 patients with known EGFR-sensitive mutations, and the EGFR-mutation status-unknown group comprised 28 patients with unknown EGFR-mutation status. Both objective response rate and disease-control rate were significantly higher in the EGFR-mutation group compared with the EGFR-unknown group (42.1% vs 14.2%, P=0.032; 94.7% vs 57.1%, P=0.005). Age, sex, smoking history, stage of disease, and tissue-sample source were not significantly correlated with the distributions of mutation status. In conclusion, it is important for advanced lung adenocarcinoma patients to undergo gene analysis before being assigned a molecularly targeted drug as first-line treatment.
机译:本研究的目的是研究EGFR突变状态与晚期肺腺癌患者治疗效果之间的相关性。共有47名接受厄洛替尼作为一线治疗的患者分为两组:EGFR基因突变组包括19名已知EGFR敏感突变的患者,EGFR突变状态未知的组包括28名EGFR突变未知的患者状态。 EGFR突变组的客观应答率和疾病控制率均显着高于未知的EGFR组(42.1%vs 14.2%,P = 0.032; 94.7%vs 57.1%,P = 0.005)。年龄,性别,吸烟史,疾病阶段和组织样本来源与突变状态的分布没有显着相关。总之,对于晚期肺腺癌患者,在为其指定分子靶向药物作为一线治疗药物之前进行基因分析非常重要。

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