用于大肠癌筛查的多靶点粪便 RNA 检测的分析验证。

IF 3.4 3区 医学 Q1 PATHOLOGY
Erica K. Barnell , Jack Land , Kimberly Kruse , Maya C. Scott , Ben Wedeking , Catherine Morrison , Clayton Grass , Ann Zuniga , Elizabeth M. Wurtzler , Eric J. Duncavage
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引用次数: 0

摘要

多靶点粪便 RNA(mt-sRNA)检验(ColoSense)是一种无创诊断检验,可筛查 45 岁及以上平均风险人群中的结直肠癌和晚期腺瘤。mt-sRNA 检验结合了市售的粪便免疫化学检验、八种 RNA 转录物的浓度以及参与者报告的吸烟状况。作为 CRC-PREVENT(结直肠癌和癌前腺瘤非侵入性检测试验)临床试验的一部分,进行了 12 项分析验证研究,以评估分析灵敏度、线性度、精确度、干扰物质、交叉反应、携带、交叉污染和稳健性。mt-sRNA 检验的分析验证结果表明,其空白极限、检测极限和定量极限分别为
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Analytical Validation of the Multitarget Stool RNA Test for Colorectal Cancer Screening

The multitarget stool RNA (mt-sRNA) test (ColoSense) is a noninvasive diagnostic test that screens for colorectal cancer and advanced adenomas in average-risk individuals aged 45 years and older. The mt-sRNA test incorporates a commercially available fecal immunochemical test, concentration of eight RNA transcripts, and participant-reported smoking status. As part of the CRC-PREVENT (Colorectal Cancer and Pre-Cancerous Adenoma Non-Invasive Detection Test) clinical trial, 12 analytical validation studies were conducted to assess analytical sensitivity, linearity, precision, interfering substances, cross-reactivity, carry-over, cross-contamination, and robustness. Analytical validation of the mt-sRNA test demonstrated limit of blank, limit of detection, and limit of quantification of <0.6, <0.7, and ≤2.5 copies/μL for all markers, respectively. The mt-sRNA test demonstrated linearity between 2.5 and 2500 copies/μL, and <20% coefficient of variation, and/or ≥95% concordance with regard to precision, interfering substances, carry-over, cross-contamination, and robustness. There was no significant impact of cross-reactivity from non–colorectal cancer diseases. These data provide a framework for laboratories to complete analytical validation for RNA-based panels that require premarket approval as a class III medical device from the US Food and Drug Administration.

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来源期刊
CiteScore
8.10
自引率
2.40%
发文量
143
审稿时长
43 days
期刊介绍: The Journal of Molecular Diagnostics, the official publication of the Association for Molecular Pathology (AMP), co-owned by the American Society for Investigative Pathology (ASIP), seeks to publish high quality original papers on scientific advances in the translation and validation of molecular discoveries in medicine into the clinical diagnostic setting, and the description and application of technological advances in the field of molecular diagnostic medicine. The editors welcome for review articles that contain: novel discoveries or clinicopathologic correlations including studies in oncology, infectious diseases, inherited diseases, predisposition to disease, clinical informatics, or the description of polymorphisms linked to disease states or normal variations; the application of diagnostic methodologies in clinical trials; or the development of new or improved molecular methods which may be applied to diagnosis or monitoring of disease or disease predisposition.
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