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Usefulness of Nanofluidic Digital PCR Arrays to Quantify T790M Mutation in EGFR-mutant Lung Adenocarcinoma

机译:纳米流体数字PCR阵列量化EGFR突变肺腺癌中T790M突变的有用性。

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Aim: The present pilot study assessed the usefulness of nanofluidic digital polymerase chain reaction (PCR) arrays in epidermal growth factor receptor (EGFR)-mutant lung adenocarcinoma after tyrosine kinase inhibitor (TKI) resistance. Patients and Methods: We enrolled 12 patients with primary lung adenocarcinoma with sensitive EGFR mutation-confirmed T790M status by re-biopsy after TKI resistance. Nanofluidic digital PCR arrays were used to quantify T790M in genomic DNA from the pre-treatment primary site and in serum cell-free DNA (cfDNA). Results: On digital PCR, quantified T790M at the pre-treatment primary site was higher in re-biopsy-positive T790M patients (n=4) than in re-biopsy-negative patients (n=8) (0.78%{+/-}0.36% vs. 0.07%{+/-}0.09%, p<0.01). T790M at the pre-treatment primary site correlated with progression-free survival (PFS) after gefitinib therapy (r=0.67, p=0.016). Conclusion: Use of digital PCR to quantify T790M at the primary site of EGFR-mutant lung adenocarcinoma predicted T790M emergence in re-biopsies after TKI resistance and PFS after gefitinib therapy.
机译:目的:本试验研究评估了酪氨酸激酶抑制剂(TKI)耐药后,纳米流体数字聚合酶链反应(PCR)阵列在表皮生长因子受体(EGFR)突变的肺腺癌中的有效性。患者和方法:我们通过对TKI耐药后的再次活检,招募了12例原发性肺腺癌患者,这些患者经EGFR突变确认为T790M状态敏感。纳米流体数字PCR阵列用于量化预处理主要位点的基因组DNA和血清无细胞DNA(cfDNA)中的T790M。结果:在数字PCR上,活检阳性的T790M患者(n = 4)在治疗前原发部位的定量T790M高于活检阴性的患者(n = 8)(0.78%{+/- } 0.36%和0.07%{+/-} 0.09%,p <0.01)。治疗前主要部位的T790M与吉非替尼治疗后的无进展生存期(PFS)相关(r = 0.67,p = 0.016)。结论:使用数字PCR定量EGFR突变型肺腺癌原发部位的T790M可预测T790M在吉非替尼治疗后的TKI耐药性和PFS后的再次活检中出现。

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