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cobas EBV 和 cobas BKV 检测方法的性能:标准化定量的多中心比较。

Performance of the cobas EBV and cobas BKV assays: multi-site comparison of standardized quantitation.

机构信息

Department of Clinical Microbiology, HUS Diagnostic Center, HUSLAB, Clinical Microbiology, University of Helsinki and Helsinki University Hospital, Helsinki, Finland.

Department of Clinical Microbiology, Aarhus University Hospital, Aarhus, Denmark.

出版信息

J Clin Microbiol. 2024 Aug 14;62(8):e0026724. doi: 10.1128/jcm.00267-24. Epub 2024 Jul 24.

Abstract

Guidelines recommend monitoring of Epstein-Barr virus (EBV) and BK virus (BKV) in solid organ and hematopoietic stem cell transplant patients. The majority of quantitative DNA testing for EBV and BKV employs unstandardized individual laboratory-developed testing solutions (LDTs), with implications for accuracy, reproducibility, and comparability between laboratories. The performance of the cobas EBV and cobas BKV assays was assessed across five laboratories, using the World Health Organization International Standards (WHO IS) for EBV and BKV, and the National Institute of Standards and Technology Quantitative Standard for BKV, and results were compared with the LDTs in use at the time. Methods were also compared using locally sourced clinical specimens. Variation was high when laboratories reported EBV or BKV DNA values using LDTs, where quantitative values were observed to differ by up to 1.5 log unit/mL between sites. Conversely, results from the cobas EBV and cobas BKV assays were accurate and reproducible across sites and on different testing days. Adjustment of LDTs using the international standards led to closer alignment between the assays; however, day-to-day reproducibility of LDTs remained high. In addition, BKV continued to show bias, indicating challenges with the commutability of the BKV International Standard. The cobas EBV and cobas BKV assays are automated, aligned to the WHO IS, and have the potential to reduce the variability in viral load testing introduced by differences in LDTs. Standardization of reporting values may eventually allow different centers to compare data to allow clinical decision thresholds to be established supporting improvements in patient management.IMPORTANCEThe application of center-specific cut-offs for clinical decisions and the variability of LDTs often hinder interpretation; thus, the findings reported here support the need for standardization in the field of post-transplant monitoring of EBV and BKV to improve patient management. Alongside the choice of assay, it is also important to consider which standard to use when deciding upon a testing methodology. This is a call to action for standardization, as treatment for EBV and BKV is driven by viral load test results, and the more accurate and comparable the test results are across institutions, the more informed and better the treatment decisions can be.

摘要

指南建议对实体器官和造血干细胞移植患者进行 EBV(Epstein-Barr 病毒)和 BKV(BK 病毒)的监测。大多数 EBV 和 BKV 的定量 DNA 检测采用非标准化的实验室自建检测解决方案(LDT),这对准确性、可重复性和实验室之间的可比性都有影响。在五个实验室中,使用 EBV 和 BKV 的世界卫生组织国际标准(WHO IS)以及 BKV 的国家标准与技术研究所定量标准,对 cobas EBV 和 cobas BKV 检测进行了评估,并将结果与当时使用的 LDT 进行了比较。还使用当地来源的临床标本比较了方法。当实验室使用 LDT 报告 EBV 或 BKV DNA 值时,差异很大,观察到定量值在不同地点之间相差高达 1.5 个对数单位/ml。相反,cobas EBV 和 cobas BKV 检测在不同的检测日和不同地点的结果都是准确且可重复的。使用国际标准对 LDT 进行调整后,检测之间的一致性更好;然而,LDT 的日常可重复性仍然很高。此外,BKV 仍存在偏差,表明 BKV 国际标准的互换性存在挑战。 cobas EBV 和 cobas BKV 检测是自动化的,与 WHO IS 一致,并有潜力减少由 LDT 差异引入的病毒载量检测中的变异性。报告值的标准化最终可能允许不同的中心比较数据,以建立临床决策阈值,支持改善患者管理。

重要性

临床决策的中心特异性截止值和 LDT 的可变性常常阻碍了对检测结果的解读;因此,这里报告的结果支持在 EBV 和 BKV 移植后监测领域进行标准化,以改善患者管理。除了检测方法的选择外,在决定检测方法时,考虑使用哪种标准也很重要。这是对标准化的呼吁,因为 EBV 和 BKV 的治疗取决于病毒载量检测结果,检测结果在机构之间越准确和可比,治疗决策就越明智和越好。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f6a5/11323559/6ec542108332/jcm.00267-24.f001.jpg

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