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Accuracy and clinical influence of plasma EGFR mutation detection in management of advanced lung adenocarcinoma

机译:血浆EGFR突变检测在晚期肺腺癌管理中的准确性和临床影响

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摘要

This study aimed to investigate the accuracy of plasma EGFR status detecting according to tissue EGFR status, and further explore the correlation of plasma EGFR status with clinicopathological features and progression-free survival (PFS) in patients with advanced lung adenocarcinoma. 157 patients with advanced lung adenocarcinoma were recruited. Paired tissue and plasma samples were collected before any prior treatments, EGFR gene mutation detection was performed using the amplification refractory mutation system (ARMS) method. EGFR mutations were detected in 81 tissue samples and the mutation rate was 51.6%, while in 50 plasma samples and the mutation rate was 31.8%. The overall concordance rate of EGFR mutations between tissue and plasma samples was 76.4%. And the sensitivity, specificity, positive predictive value and negative predictive value of the EGFR detection using plasma samples were 94.0%, 68.2%, 58.0 and 96.1% respectively. Patients with no-smoking (P = 0.039) and more number of metastatic sites (P = 0.012) presented a higher EGFR mutation frequency in plasma, but no association of plasma EGFR mutation with other clinicopathological features and PFS by targeted therapy was discovered. This study revealed that plasma EGFR mutation detection might be regarded as a good alternative biomarker for lung adenocarcinoma management, especially for patients who were not tolerant with obtainment of tissue samples, but further prognostic value needs to be investigated.
机译:本研究旨在探讨根据组织EGFR状况检测血浆EGFR状况的准确性,并进一步探讨晚期肺腺癌患者血浆EGFR状况与临床病理特征和无进展生存期(PFS)的相关性。招募了157例晚期肺腺癌患者。在进行任何之前的治疗之前,先收集配对的组织和血浆样品,然后使用扩增难治性突变系统(ARMS)方法进行EGFR基因突变检测。在81个组织样品中检测到EGFR突变,突变率为51.6%,而在50个血浆样品中检测到EGFR的突变率为31.8%。组织与血浆样品之间EGFR突变的总体一致性率为76.4%。用血浆样品检测EGFR的敏感性,特异性,阳性预测值和阴性预测值分别为94.0%,68.2%,58.0和96.1%。禁止吸烟(P = 0.039)和转移部位较多(P = 0.012)的患者血浆中EGFR突变频率较高,但通过靶向治疗未发现血浆EGFR EGFR突变与其他临床病理特征和PFS相关。这项研究表明,血浆EGFR突变检测可能被认为是治疗肺腺癌的良好替代生物标志物,特别是对于那些对组织样本的采集不耐受的患者,但还需要进一步研究其预后价值。

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