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Validation of Standards for Quantitative Assessment of JAK2 c.1849G>T (p.V617F) Allele Burden Analysis in Clinical Samples

机译:临床样品中JAK2 c.1849G> T(p.V617F)等位基因负荷分析定量评估标准的验证

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摘要

The substitution of valine with phenylalanine at amino acid 617 of the Janus kinase 2 (JAK2) gene (JAK2 p.V617F) occurs in a high proportion of patients with myeloproliferative neoplasms (MPNs). The ability to accurately measure JAK2 p.V617F allele burden is of great interest given the diagnostic relevance of the mutation and the ongoing clinical evaluation of JAK inhibitors. A main hurdle in developing quantitative assays for allele burden measurement is the unavailability of accurate standards for both assay validation and use in a standard curve for quantification. We describe our approach to the validation of standards for quantitative assessment of JAK2 p.V617F allele burden in clinical MPN samples. These standards were used in two JAK2 p.V617F assays, which were used to support clinical studies of ruxolitinib (Jakafi~®) in myelofibrosis, a real-time polymerase chain reaction assay for initial screening of all samples, and a novel single-nucleotide polymorphism typing (SNaP-shot)-based assay for samples with less than 5% mutant allele burden. Comparisons of allele burden data from clinical samples generated with these assays show a high degree of concordance with each other and with a pyrosequencing-based assay used for clinical reporting from an independent laboratory, thus providing independent validation to the accuracy of these standards.
机译:Janus激酶2(JAK2)基因(JAK2 p.V617F)氨基酸617处的缬氨酸被苯丙氨酸取代在许多患有骨髓增生性肿瘤(MPN)的患者中发生。鉴于突变的诊断意义和正在进行的JAK抑制剂临床评估,准确测量JAK2 p.V617F等位基因负荷的能力引起了人们的极大兴趣。开发用于等位基因负荷测量的定量测定法的主要障碍是无法获得用于测定法验证的准确标准品以及在定量的标准曲线中的使用。我们描述了我们的方法,用于验证临床MPN样本中JAK2 p.V617F等位基因负担的定量评估标准的方法。这些标准品已用于两次JAK2 p.V617F分析中,用于支持ruxolitinib(Jakafi®)在骨髓纤维化中的临床研究,用于实时筛选所有样品的实时聚合酶链反应分析和一种新型单核苷酸基于多态性分型(SNaP射击)的分析,突变体等位基因负担少于5%。用这些测定法生成的临床样品中的等位基因负荷数据的比较表明,彼此之间以及与基于焦磷酸测序的测定法(用于独立实验室进行临床报告)的一致性很高,因此可以独立验证这些标准的准确性。

著录项

  • 来源
    《Genetic testing and molecular biomarkers》 |2013年第5期|429-437|共9页
  • 作者单位

    Incyte Corporation, Wilmington, Delaware;

    Department of Hematopathology, The University of Texas M.D. Anderson Cancer Center, Houston, Texas;

    Incyte Corporation, Wilmington, Delaware;

    Incyte Corporation, Wilmington, Delaware;

    Department of Hematopathology, The University of Texas M.D. Anderson Cancer Center, Houston, Texas;

    Incyte Corporation, Wilmington, Delaware;

    Incyte Corporation, Wilmington, Delaware;

    Incyte Corporation, Wilmington, Delaware;

    Leukemia Department, The University of Texas M.D. Anderson Cancer Center, Houston, Texas;

    Incyte Corporation, Wilmington, Delaware,Incyte Corporation Route 141 and Henry Clay Road Experimental Station E336/237B Wilmington, DE 19880;

  • 收录信息 美国《科学引文索引》(SCI);美国《化学文摘》(CA);
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

  • 入库时间 2022-08-17 13:17:35

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