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Performance of Oncomine Fusion Transcript kit for formalin‐fixed, paraffin‐embedded lung cancer specimens

机译:福尔马林固定,石蜡包埋的肺癌标本的Oncomine Fusion Transcript试剂盒的性能

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Gene fusions play an important role in the carcinogenesis of lung adenocarcinoma. The recent association of four oncogenic driver genes, ALK , ROS1 , RET , and NTRK1 , as lung tumor predictive biomarkers has increased the need for precision medicine. We used formalin‐fixed, paraffin‐embedded tissue samples of non‐small cell lung cancer from 150 EGFR mutation‐negative cases and 10 fusion status‐known cases and compared the performance of the Oncomine Dx Fusion Transcript Test (ODxFT) with FISH break‐apart for the detection of ALK , RET , and ROS1 fusion genes. RNA was extracted from the paraffin‐embedded tissue samples with or without macrodissection under hematoxylin and eosin staining, and the ALK fusion gene was independently determined using these assays. Fusion detection analyses were successfully carried out using ODxFT in 150 cases, with only one invalid case. ALK fusion genes were detected at a frequency of 7.3% (11/150) in the lung cancer specimens. Concordance rate between the ODxFT and ALK ‐FISH analyses was 99.3% (148/149). Sensitivity and specificity were 91.7% and 99.3%, respectively. All the samples with a known fusion status were accurately matched between the two assays. Our results show a high concordance rate between the ODxFT and ALK ‐FISH analyses. ODxFT was thus validated as an effective method for detecting clinically significant ALK fusion genes in paraffin‐embedded tissue samples.
机译:基因融合在肺腺癌的癌变过程中起着重要作用。肺癌预测生物标志物四个致癌驱动基因ALK,ROS1,RET和NTRK1的最新关联增加了对精准医学的需求。我们使用来自150例EGFR突变阴性病例和10例融合状态已知病例的非小细胞肺癌的福尔马林固定,石蜡包埋的组织样本,并将Oncomine Dx融合转录本测试(ODxFT)与FISH断裂的性能进行了比较。分别用于检测ALK,RET和ROS1融合基因。在苏木精和曙红染色下,从有或没有宏观解剖的石蜡包埋组织样品中提取RNA,并使用这些测定法独立确定ALK融合基因。使用ODxFT成功进行了融合检测分析,其中有150例无效。在肺癌标本中检出ALK融合基因的频率为7.3%(11/150)。 ODxFT和ALK-FISH分析之间的一致性率为99.3%(148/149)。敏感性和特异性分别为91.7%和99.3%。在两种测定法之间准确匹配了具有已知融合状态的所有样品。我们的结果表明ODxFT与ALK-FISH分析之间的一致性很高。因此,ODxFT被证明是检测石蜡包埋的组织样品中临床上重要的ALK融合基因的有效方法。

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