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A Multi-Center, Real-Life Experience on Liquid Biopsy Practice for EGFR Testing in Non-Small Cell Lung Cancer (NSCLC) Patients

机译:非小型细胞肺癌(NSCLC)患者EGFR检测液体活检实践的多中心,现实生活经验

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摘要

Background: circulating tumor DNA (ctDNA) is a source of tumor genetic material for EGFR testing in NSCLC. Real-word data about liquid biopsy (LB) clinical practice are lacking. The aim of the study was to describe the LB practice for EGFR detection in North Eastern Italy. Methods: we conducted a multi-regional survey on ctDNA testing practices in lung cancer patients. Results: Median time from blood collection to plasma separation was 50 min (20–120 min), median time from plasma extraction to ctDNA analysis was 24 h (30 min–5 days) and median turnaround time was 24 h (6 h–5 days). Four hundred and seventy five patients and 654 samples were tested. One hundred and ninety-two patients were tested at diagnosis, with 16% EGFR mutation rate. Among the 283 patients tested at disease progression, 35% were T790M+. Main differences in LB results between 2017 and 2018 were the number of LBs performed for each patient at disease progression (2.88 vs. 1.2, respectively) and the percentage of T790M+ patients (61% vs. 26%).
机译:背景:循环肿瘤DNA(CTDNA)是NSCLC中EGFR测试的肿瘤遗传物质来源。缺乏关于液体活检(LB)临床实践的真实词数据。该研究的目的是描述意大利东北部EGFR检测的LB实践。方法:对肺癌患者的CTDNA测试实践进行了多区域调查。结果:从血液收集到血浆分离的中值时间为50分钟(20-120分钟),从等离子体提取到CTDNA分析的中值时间为24小时(30分钟 - 5天),中间周转时间为24小时(6 H-5天)。测试了四百七十五名患者和654个样品。在诊断中测试一百九十二名患者,具有16%的EGFR突变率。在疾病进展中测试的283名患者中,35%是T790M +。 2017年和2018年的LB结果的主要差异是对疾病进展的每位患者的磅数(分别为2.88 vs.2,分别为1.2)和T790M +患者的百分比(61%vs.26%)。

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