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一种基于尿液的基因组检测改善了根据美国泌尿外科学会指南分层的高危血尿患者的风险分层。

A Urine-based Genomic Assay Improves Risk Stratification for Patients with High-risk Hematuria Stratified According to the American Urological Association Guidelines.

作者信息

de Jong Joep J, Pijpers Olga M, van Kessel Kim E M, Boormans Joost L, Van Criekinge Wim, Zwarthoff Ellen C, Lotan Yair

机构信息

Department of Urology, Erasmus MC Urothelial Cancer Research Group, Rotterdam, The Netherlands.

Department of Urology, Erasmus MC Urothelial Cancer Research Group, Rotterdam, The Netherlands.

出版信息

Eur Urol Oncol. 2023 Apr;6(2):183-189. doi: 10.1016/j.euo.2022.08.002. Epub 2022 Sep 8.

Abstract

BACKGROUND

According to the recent American Urological Association (AUA) guideline on hematuria, patients are stratified into groups with low, intermediate, and high risk of urothelial carcinoma (UC). These risk groups are based on clinical factors and do not incorporate urine-based tumor markers.

OBJECTIVE

To evaluate whether a urine-based genomic assay improves the redefined AUA risk stratification for hematuria.

DESIGN, SETTING, AND PARTICIPANTS: We selected patients with complete biomarker status, as assessed on urinary DNA, from a previously collected prospective Dutch hematuria cohort (n = 838). Patients were stratified into the AUA risk categories on the basis of sex, age, and type of hematuria. Biomarker status included mutation status for the FGFR3, TERT, and HRAS genes, and methylation status for the OTX1, ONECUT2, and TWIST1 genes.

OUTCOME MEASUREMENTS AND STATISTICAL ANALYSIS

The primary endpoint was the diagnostic model performance for different hematuria risk groups. Further analyses assessed the pretest and post-test UC probability in the hematuria subgroups using a Fagan nomogram.

RESULTS AND LIMITATIONS

Overall, 65 patients (7.8%) were classified as low risk, 106 (12.6%) as intermediate risk, and 667 (79.6%) as high risk. The UC incidence differed significantly between the gross hematuria (21%, 98/457) and microscopic hematuria (4%, 14/381) groups (p < 0.001). All cancer cases were in the high-risk group, which had UC incidence of 16.8% (112/667). Application of the diagnostic model revealed robust performance among all risk groups (area under the receiver operating characteristic curve 0.929-0.971). Depending on the risk group evaluated, a negative urine assay was associated with post-test UC probability of 0.3-2%, whereas a positive urine assay was associated with post-test UC probability of 31-42%.

CONCLUSIONS

This study shows the value that a urine-based genomic assay adds to the AUA guideline stratification for patients with hematuria. It seems justified to safely withhold cystoscopy for patients with AUA low risk who have a negative urine assay. In addition, evaluation should be expedited for patients with AUA intermediate or high risk and a positive urine assay.

PATIENT SUMMARY

Patients who have blood in their urine (hematuria) can be classified as having low, intermediate, or high risk of having cancer in their urinary tract. We found that use of a urine-based genetic test improves the accuracy of predicting which patients are most likely to have cancer. Patients with a negative test may be able to avoid invasive tests, while further tests could be prioritized for patients with a positive test.

摘要

背景

根据美国泌尿外科学会(AUA)最近关于血尿的指南,患者被分为低、中、高风险的尿路上皮癌(UC)组。这些风险组基于临床因素,未纳入基于尿液的肿瘤标志物。

目的

评估基于尿液的基因组检测是否能改善重新定义的AUA血尿风险分层。

设计、设置和参与者:我们从之前收集的荷兰前瞻性血尿队列(n = 838)中选择了尿DNA检测生物标志物状态完整的患者。根据性别、年龄和血尿类型将患者分层为AUA风险类别。生物标志物状态包括FGFR3、TERT和HRAS基因的突变状态,以及OTX1、ONECUT2和TWIST1基因的甲基化状态。

结果测量和统计分析

主要终点是不同血尿风险组的诊断模型性能。进一步分析使用Fagan列线图评估血尿亚组中检测前和检测后的UC概率。

结果与局限性

总体而言,65名患者(7.8%)被归类为低风险,106名(12.6%)为中风险,667名(79.6%)为高风险。肉眼血尿组(21%,98/457)和镜下血尿组(4%,14/381)的UC发病率差异显著(p < 0.001)。所有癌症病例均在高风险组,其UC发病率为16.8%(112/667)。诊断模型的应用在所有风险组中均显示出强大的性能(受试者操作特征曲线下面积为0.929 - 0.971)。根据评估的风险组不同,尿液检测阴性与检测后UC概率为0.3 - 2%相关,而尿液检测阳性与检测后UC概率为31 - 42%相关。

结论

本研究显示了基于尿液的基因组检测对AUA血尿患者指南分层的价值。对于尿液检测阴性的AUA低风险患者安全地免除膀胱镜检查似乎是合理的。此外,对于AUA中或高风险且尿液检测阳性的患者应加快评估。

患者总结

有血尿的患者可被分类为尿路患癌风险低、中或高。我们发现使用基于尿液的基因检测可提高预测哪些患者最有可能患癌的准确性。检测阴性的患者可能能够避免侵入性检查,而检测阳性的患者可优先进行进一步检查。

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