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A multigene urine test for the detection and stratification of bladder cancer in patients presenting with hematuria

机译:多基因尿液检测可对血尿患者的膀胱癌进行检测和分层

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Purpose: We investigated whether the RNA assay uRNA? and its derivative Cxbladder? have greater sensitivity for the detection of bladder cancer than cytology, NMP22? BladderChek? and NMP22? ELISA, and whether they are useful in risk stratification. Materials and Methods: A total of 485 patients presenting with gross hematuria but without a history of urothelial cancer were recruited prospectively from 11 urology clinics in Australasia. Voided urine samples were obtained before cystoscopy. The sensitivity and specificity of the RNA tests were compared to cytology and the NMP22 assays using cystoscopy as the reference. The ability of Cxbladder to distinguish between low grade, stage Ta urothelial carcinoma and more advanced urothelial carcinoma was also determined. Results: uRNA detected 41 of 66 urothelial carcinoma cases (62.1% sensitivity, 95% CI 49.3-73.8) compared with NMP22 ELISA (50.0%, 95% CI 37.4-62.6), BladderChek (37.9%, 95% CI 26.2-50.7) and cytology (56.1%, 95% CI 43.8-68.3). Cxbladder, which was developed on the study data, detected 82%, including 97% of the high grade tumors and 100% of tumors stage 1 or greater. The cutoffs for uRNA and Cxbladder were prespecified to give a specificity of 85%. The specificity of cytology was 94.5% (95% CI 91.9-96.5), NMP22 ELISA 88.0%, (95% CI 84.6-91.0) and BladderChek 96.4% (95% CI 94.2-98.0). Cxbladder distinguished between low grade Ta tumors and other detected urothelial carcinoma with a sensitivity of 91% and a specificity of 90%. Conclusions: uRNA and Cxbladder showed improved sensitivity for the detection of urothelial carcinoma compared to the NMP22 assays. Stratification with Cxbladder provides a potential method to prioritize patients for the management of waiting lists.
机译:目的:我们调查了RNA分析是否为uRNA?及其衍生的Cxbladder? NMP22对膀胱癌的检测比对细胞学有更高的敏感性? BladderChek?和NMP22? ELISA,以及它们是否可用于风险分层。资料与方法:前瞻性从澳大拉西亚的11个泌尿科门诊招募了485例有严重血尿但无尿路上皮癌病史的患者。膀胱镜检查前已获取尿样。使用膀胱镜检查作为参考,将RNA检测的敏感性和特异性与细胞学和NMP22检测进行了比较。还确定了Cxbladder区分低度,分期Ta尿路上皮癌和较晚期尿路上皮癌的能力。结果:uRNA检测到66例尿路上皮癌病例中的41例(敏感性62.1%,95%CI 49.3-73.8),而NMP22 ELISA(50.0%,95%CI 37.4-62.6),BladderChek(37.9%,95%CI 26.2-50.7)和细胞学检查(56.1%,95%CI 43.8-68.3)。根据研究数据开发的Cxbladder检测到82%,包括97%的高级别肿瘤和100%的1期或更高级别的肿瘤。预先确定了uRNA和Cxbladder的临界值,特异性为85%。细胞学特异性为94.5%(95%CI 91.9-96.5),NMP22 ELISA 88.0%(95%CI 84.6-91.0)和BladderChek 96.4%(95%CI 94.2-98.0)。 Cxbladder区分低度Ta肿瘤和其他检测到的尿路上皮癌,敏感性为91%,特异性为90%。结论:与NMP22分析相比,uRNA和Cxbladder对尿路上皮癌的检测灵敏度更高。 Cxbladder的分层提供了一种潜在的方法,可以优先考虑患者的等待名单管理。

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