Performance of a Rapid Digital PCR Test for the Detection of Non-Small Cell Lung Cancer (NSCLC) Variants.

IF 4.1 3区 医学 Q1 GENETICS & HEREDITY Molecular Diagnosis & Therapy Pub Date : 2024-11-01 Epub Date: 2024-08-02 DOI:10.1007/s40291-024-00732-y
Abdulaziz F Al Mana, Kristen Culp, Abby Keeler, Orlando Perrera, Malini Rajagopalan, Lucien Jacky, Brad Brown, Bharat Thyagarajan
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Abstract

Background: Next-generation sequencing is widely used for comprehensive molecular profiling for many cancers including lung cancer. However, the complex workflows and long turnaround times limit its access and utility. ChromaCode's High Definition PCR Non-Small Cell Lung Cancer Panel (HDPCR™ NSCLC Panel) is a low-cost, rapid turnaround, digital polymerase chain reaction assay that is designed to detect variants in nine NSCLC genes listed in National Comprehensive Cancer Network guidelines.

Methods: This assay uses TaqMan® probe limiting chemistry and proprietary analysis software to enable multi-target detection within a single-color channel. We compared the performance of the HDPCR™ NSCLC Panel against an in-house, laboratory-developed, targeted next-generation sequencing panel used in the Molecular Diagnostics Laboratory at the University of Minnesota Medical Center to detect biomarkers for NSCLC.

Results: The overall accuracy of the HDPCR panel was 99.48% (95% confidence interval 99.01-99.76) with a sensitivity of 95.35% (95% confidence interval 88.52-98.72) and a specificity of 99.69% (95% confidence interval 99.29-99.90). The HDPCR wet lab workflow was 4 h, and the time to generate variant calls from raw data using the ChromaCode Cloud was 2 minutes.

Conclusions: We demonstrated that the HDPCR™ NSCLC Panel provides timely, comprehensive, and sensitive mutation detection in NSCLC samples with results in less than 24 h.

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用于检测非小细胞肺癌 (NSCLC) 变异的快速数字 PCR 检测仪的性能。
背景:新一代测序技术被广泛用于包括肺癌在内的多种癌症的综合分子图谱分析。然而,复杂的工作流程和较长的周转时间限制了其使用和实用性。ChromaCode 的高清 PCR 非小细胞肺癌检测试剂盒(HDPCR™ NSCLC Panel)是一种低成本、周转快的数字聚合酶链反应检测试剂盒,旨在检测美国国家综合癌症网络指南中列出的 9 个 NSCLC 基因的变异:该测定使用 TaqMan® 探针限幅化学和专有分析软件,可在单色通道内进行多目标检测。我们将 HDPCR™ NSCLC 检测板的性能与明尼苏达大学医学中心分子诊断实验室用于检测 NSCLC 生物标记物的内部实验室开发的靶向新一代测序检测板进行了比较:HDPCR 小组的总体准确率为 99.48%(95% 置信区间为 99.01-99.76),灵敏度为 95.35%(95% 置信区间为 88.52-98.72),特异性为 99.69%(95% 置信区间为 99.29-99.90)。HDPCR湿实验室工作流程为4小时,使用ChromaCode云从原始数据生成变异调用的时间为2分钟:我们证明了 HDPCR™ NSCLC Panel 能及时、全面、灵敏地检测 NSCLC 样本中的突变,并在 24 小时内得出结果。
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来源期刊
CiteScore
7.80
自引率
2.50%
发文量
53
审稿时长
>12 weeks
期刊介绍: Molecular Diagnosis & Therapy welcomes current opinion articles on emerging or contentious issues, comprehensive narrative reviews, systematic reviews (as outlined by the PRISMA statement), original research articles (including short communications) and letters to the editor. All manuscripts are subject to peer review by international experts.
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