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Targeted RNA sequencing with touch imprint cytology samples for non‐small cell lung cancer patients

机译:针对非小细胞肺癌患者的触摸印记细胞学样本的靶向RNA测序

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BACKGROUND:RNA-based sequencing is considered ideal for detecting pathogenic fusion-genes compared to DNA-based assays and provides valuable information about the relative expression of driver genes. However, RNA from formalin-fixed paraffin-embedded tissue has issues with both quantity and quality, making RNA-based sequencing difficult in clinical practice. Analyzing stamp-derived RNA with next-generation sequencing (NGS) can address the above-mentioned obstacles. In this study, we validated the analytical specifications and clinical performance of our custom panel for RNA-based assays on the Ion Torrent platform.METHODS:To evaluate our custom RNA lung panel, we first examined the gene sequences of RNA derived from 35 NSCLC tissues with diverse backgrounds by conventional methods and NGS. Next, we moved to the clinical phase, where clinical samples (all stamp-derived RNA) were used to examine variants. In the clinical phase we conducted an NGS analysis while simultaneously applying conventional approaches to assess the feasibility and validity of the panel in clinical practice.RESULTS:In the prerun phase, all of the variants confirmed with conventional methods were detected by NGS. In the clinical phase, a total of 80 patients were enrolled and 80 tumor specimens were sequenced from February 2018 to December 2018. There were 66 cases in which the RNA concentration was too low to be measured, but sequencing was successful in the vast majority of cases. The concordance between NGS and conventional methods was 95.0%.CONCLUSIONS:RNA extraction using stamp specimens and panel sequencing by NGS were considered applicable in clinical settings.KEY POINTS:Significant findings of the study Next-generation sequencing using RNA from stamp specimens was able to detect driver gene changes in non-small cell lung cancer including fusion genes with the same accuracy as conventional methods. What this study adds Using RNA from stamp specimens obtained from biopsy increases the number of candidate cases for RNA sequencing in clinical settings.? 2020 The Authors. Thoracic Cancer published by China Lung Oncology Group and John Wiley & Sons Australia, Ltd.
机译:背景技术基于RNA的测序被认为是与基于DNA的测定相比检测致病性融合基因的理想选择,并提供有关驾驶员基因的相对表达的有价值的信息。然而,来自福尔马林固定的石蜡包埋的组织的RNA具有数量和质量的问题,使RNA的测序在临床实践中难以。分析具有下一代测序(NGS)的印章衍生的RNA可以解决上述障碍物。在这项研究中,我们验证了我们定制面板的分析规范和临床表现,用于离子Torrent平台上的基于RNA的测定。方法:评估我们的定制RNA肺部面板,首先检查来自35个NSCLC组织的RNA的基因序列通过传统方法和NGS与不同的背景。接下来,我们移动到临床阶段,其中使用临床样本(所有印模RNA)来检查变体。在临床期间,我们进行了NGS分析,同时应用常规方法来评估临床实践中面板的可行性和有效性。结果:在普鲁阶段,通过NGS检测用常规方法证实的所有变体。在临床阶段,共征收80例患者,并从2018年2月到2018年2月测定了80例肿瘤标本。66例病例,其中RNA浓度太低才能测量,但排序在绝大多数中成功案件。 NGS和常规方法之间的一致性是95.0%。结论:使用NGS的RNA提取和NGS的面板测序适用于临床环境.KEY点:使用RNA从盖印标本中的RNA的研究下一代测序的显着发现能够检测非小细胞肺癌中的驱动基因变化,包括融合基因,其精度与常规方法相同。本研究添加使用从活检中获得的印模标本的RNA增加的研究增加了临床环境中RNA测序的候选病例的数量。? 2020作者。中国肺部肿瘤集团和约翰瓦里和儿子澳大利亚发表的胸癌

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