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Cxbladder检测、分流和监测的分析验证:尿路上皮癌检测与管理的检测方法

Analytical Validation of Cxbladder Detect, Triage, and Monitor: Assays for Detection and Management of Urothelial Carcinoma.

作者信息

Harvey Justin C, Cambridge Lisa M, Ellen Charles W, Colonval Megan, Hazlett Jody A, Newell Jordan, Zhou Xin, Guilford Parry J

机构信息

Pacific Edge Diagnostics NZ, Ltd., 87 St. David Street, Dunedin 9016, New Zealand.

Cambridge Quality Consulting, T/A Check Electric Ltd., 204 Coast Road, Waikouaiti 9471, New Zealand.

出版信息

Diagnostics (Basel). 2024 Sep 17;14(18):2061. doi: 10.3390/diagnostics14182061.

Abstract

: Cxbladder assays are reverse transcription-quantitative polymerase chain reaction (RT-qPCR) tests incorporating five genetic biomarkers (, , , , and ) to provide risk stratification for urothelial carcinoma (UC) in patients with hematuria or undergoing surveillance for recurrent disease. This study evaluated the analytical validity of the Cxbladder Detect, Triage, and Monitor assays. Pre-specified acceptance criteria, including the assays' fundamental aspects (sample and reagent stability, RNA extraction quality, RT-qPCR linearity, and analytical sensitivity and specificity), accuracy and precision, and reproducibility between laboratories. Cxbladder had an analytical sensitivity of 12.5-31.1 RNA copies/mL urine for the , , , and UC biomarkers and 68.9 RNA copies/mL for the inflammatory biomarker . All the pre-specified analytical criteria were met. Cxbladder had diagnostic sensitivity, specificity, positive predictive value, and negative predictive values of 77%, 94%, 68%, and 96%, respectively, for Detect; 95%, 46%, 20%, and 98% for Triage; and 91%, 39%, 21%, and 96% for Monitor. Cxbladder had high analytical accuracy (≤10.63% inaccuracy across all biomarkers) and good reproducibility (>85% concordance between laboratories). Cxbladder accurately and reproducibly detects UC biomarker expression and can aid clinicians in risk stratification of hematuria patients or those undergoing surveillance for recurrent UC.

摘要

Cxbladder检测是一种逆转录定量聚合酶链反应(RT-qPCR)检测,纳入了五种基因生物标志物(、、、和),可为血尿患者或接受复发性疾病监测的尿路上皮癌(UC)患者提供风险分层。本研究评估了Cxbladder检测、分类和监测检测的分析有效性。预先指定的验收标准,包括检测的基本方面(样本和试剂稳定性、RNA提取质量、RT-qPCR线性以及分析灵敏度和特异性)、准确性和精密度以及实验室间的可重复性。Cxbladder对、、、和UC生物标志物的分析灵敏度为12.5 - 31.1个RNA拷贝/毫升尿液,对炎症生物标志物的灵敏度为68.9个RNA拷贝/毫升。所有预先指定的分析标准均得到满足。Cxbladder检测的诊断灵敏度、特异性、阳性预测值和阴性预测值分别为77%、94%、68%和96%;分类检测为95%、46%、20%和98%;监测检测为91%、39%、21%和96%。Cxbladder具有较高的分析准确性(所有生物标志物的不准确性≤10.63%)和良好的可重复性(实验室间一致性>85%)。Cxbladder能够准确且可重复地检测UC生物标志物的表达,并可帮助临床医生对血尿患者或接受复发性UC监测的患者进行风险分层。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3058/11431456/a645f2ae537c/diagnostics-14-02061-g001.jpg

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