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酪氨酸激酶抑制剂治疗失败后非小细胞肺癌中T790M突变检测的扩增阻滞突变系统、超级扩增阻滞突变系统和液滴数字PCR的比较

Comparison of the Amplification Refractory Mutation System, Super Amplification Refractory Mutation System, and Droplet Digital PCR for T790 M Mutation Detection in Non-small Cell Lung Cancer after Failure of Tyrosine Kinase Inhibitor Treatment.

作者信息

Zhu Lucheng, Zhang Shirong, Xun Yanping, Jiang Yanping, Xia Bing, Chen Xueqin, Wang Limin, Jiang Hong, Ma Shenglin

机构信息

Department of Oncology, Hangzhou First People's Hospital, Nanjing Medical University, No. 261, Huansha Road, Shangcheng District, Hangzhou, 310006, People's Republic of China.

Department of Oncology, Hangzhou Cancer Hospital, Hangzhou, China.

出版信息

Pathol Oncol Res. 2018 Oct;24(4):843-851. doi: 10.1007/s12253-017-0286-3. Epub 2017 Sep 3.

Abstract

Plasma mutation detection has the advantages of non-invasiveness and accessibility. Here, we evaluated three methods, the amplification refractory mutation system (ARMS), second-generation ARMS (SuperARMS), and droplet digital PCR (ddPCR), to assess their concordance and feasibility for the detection of mutations in plasma samples. Non-small lung cancer patients with stage IIIB/IV that were resistant to epidermal growth factor receptor-tyrosine kinase inhibitor (EGFR-TKI) treatment were enrolled. Blood samples were collected within 14 days after TKI resistance. Each sample was simultaneously assessed by the three methods. In total, 169 patients were enrolled; 54.4% were female, 72.2% were diagnosed with stage IV disease; and 97.6% had adenocarcinoma. T790 M mutations were detected in 42 (24.8%) of the 169 samples using ARMS, one of which carried the T790 M alone, 22 that also encoded exon 19 deletions, and 19 with L858R mutations. For the SuperARMS assay, 59 (34.9%) samples exhibited the T790 M mutation, and 110 (65.1%) showed no detectable T790 M mutation. ddPCR showed that 61 (36.1%) samples contained the T790 M mutation, whereas 108 (63.9%) were not positive. T790 M abundance ranged from 0.04% to 38.2%. The median T790 M abundance was 0.15% for total samples and 2.98% for T790 M mutation samples. The overall concordance was 78.7% (133/169) among ARMS, SuperARMS, and ddPCR. Compared with patients with stage III disease, patients with stage IV disease exhibited a higher T790 M mutation detection rate (28.7% vs. 14.9% by ARMS; 37.7% vs. 27.7% by SuperARMS; and 41.8% vs. 21.3% by ddPCR). Liquid biopsy showed promise and has the advantages of non-invasiveness and accessibility. T790 M detection based on circulating tumor DNA showed high concordance. Compared with non-digital platforms, ddPCR showed higher sensitivity and provided both frequency and abundance information, which might be important for treatment decisions.

摘要

血浆突变检测具有非侵入性和易获取性的优点。在此,我们评估了三种方法,即扩增阻滞突变系统(ARMS)、第二代ARMS(SuperARMS)和液滴数字PCR(ddPCR),以评估它们在检测血浆样本突变中的一致性和可行性。纳入了对表皮生长因子受体酪氨酸激酶抑制剂(EGFR-TKI)治疗耐药的IIIB/IV期非小细胞肺癌患者。在TKI耐药后14天内采集血样。每个样本同时用这三种方法进行评估。总共纳入了169例患者;54.4%为女性,72.2%被诊断为IV期疾病;97.6%患有腺癌。使用ARMS在169个样本中的42个(24.8%)检测到T790M突变,其中1个仅携带T790M,22个同时编码外显子19缺失,19个伴有L858R突变。对于SuperARMS检测,59个(34.9%)样本显示T790M突变,110个(65.1%)未检测到T790M突变。ddPCR显示61个(36.1%)样本含有T790M突变,而108个(63.9%)为阴性。T790M丰度范围为0.04%至38.2%。所有样本的T790M丰度中位数为0.15%,T790M突变样本的中位数为2.98%。ARMS、SuperARMS和ddPCR之间的总体一致性为78.7%(133/169)。与III期疾病患者相比,IV期疾病患者的T790M突变检测率更高(ARMS检测分别为28.7%对14.9%;SuperARMS检测分别为37.7%对27.7%;ddPCR检测分别为41.8%对21.3%)。液体活检显示出前景,具有非侵入性和易获取性的优点。基于循环肿瘤DNA的T790M检测显示出高度一致性。与非数字平台相比,ddPCR显示出更高的灵敏度,并提供了频率和丰度信息,这可能对治疗决策很重要。

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