首页> 外文期刊>JAMA: the Journal of the American Medical Association >Detection of bladder cancer using a point-of-care proteomic assay.
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Detection of bladder cancer using a point-of-care proteomic assay.

机译:使用即时护理蛋白质组学检测膀胱癌。

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CONTEXT: A combination of methods is used for diagnosis of bladder cancer because no single procedure detects all malignancies. Urine tests are frequently part of an evaluation, but have either been nonspecific for cancer or required specialized analysis at a laboratory. OBJECTIVE: To investigate whether a point-of-care proteomic test that measures the nuclear matrix protein NMP22 in voided urine could enhance detection of malignancy in patients with risk factors or symptoms of bladder cancer. DESIGN, SETTING, AND PATIENTS: Twenty-three academic, private practice, and veterans' facilities in 10 states prospectively enrolled consecutive patients from September 2001 to May 2002. Participants included 1331 patients at elevated risk for bladder cancer due to factors such as history of smoking or symptoms including hematuria and dysuria. Patients at risk for malignancy of the urinary tract provided a voided urine sample for analysis of NMP22 protein and cytology prior to cystoscopy. MAIN OUTCOME MEASURES: The diagnosis of bladder cancer, based on cystoscopy with biopsy, was accepted as the reference standard. The performance of the NMP22 test was compared with voided urine cytology as an aid to cancer detection. Testing for the NMP22 tumor marker was conducted in a blinded manner. RESULTS: Bladder cancer was diagnosed in 79 patients. The NMP22 assay was positive in 44 of 79 patients with cancer (sensitivity, 55.7%; 95% confidence interval [CI], 44.1%-66.7%), whereas cytology test results were positive in 12 of 76 patients (sensitivity, 15.8%; 95% CI, 7.6%-24.0%). The specificity of the NMP22 assay was 85.7% (95% CI, 83.8%-87.6%) compared with 99.2% (95% CI, 98.7%-99.7%) for cytology. The proteomic marker detected 4 cancers that were not visualized during initial endoscopy, including 3 that were muscle invasive and 1 carcinoma in situ. CONCLUSION: The noninvasive point-of-care assay for elevated urinary NMP22 protein can increase the accuracy of cystoscopy, with test results available during the patient visit.
机译:背景:由于没有单一的程序可以检测出所有的恶性肿瘤,因此将多种方法用于膀胱癌的诊断。尿液检查经常是评估的一部分,但要么对癌症没有特异性,要么需要在实验室进行专门分析。目的:探讨一种在尿液中检测核基质蛋白NMP22的现场蛋白质组学检测方法是否可以增强对具有危险因素或膀胱癌症状的患者的恶性检测。设计,地点和患者:2001年9月至2002年5月在美国10个州的23个学术,私人执业和退伍军人医疗机构连续招募了患者。研究对象包括1331名因罹患膀胱癌史等因素而罹患膀胱癌的风险较高的患者。吸烟或包括血尿和排尿困难的症状。在膀胱镜检查之前,有尿路恶性风险的患者提供了尿液样本,用于分析NMP22蛋白和细胞学。主要观察指标:以膀胱镜活检为基础的膀胱癌诊断为参考标准。将NMP22测试的性能与尿液细胞学检查作为癌症检测的辅助手段进行了比较。 NMP22肿瘤标志物的测试以盲法进行。结果:79例患者被诊断出膀胱癌。 NMP22检测在79例癌症患者中有44例呈阳性(敏感性为55.7%; 95%置信区间[CI]为44.1%-66.7%),而细胞学检测结果为76例患者中的12例呈阳性(敏感性为15.8%; 95%CI,7.6%-24.0%)。 NMP22检测的特异性为85.7%(95%CI,83.8%-87.6%),而细胞学检查的特异性为99.2%(95%CI,98.7%-99.7%)。蛋白质组学标记物检测了4种在初始内窥镜检查期间未发现的癌症,包括3种是肌肉浸润性癌和1种原位癌。结论:尿液中NMP22蛋白升高的非侵入性即时检测可以提高膀胱镜检查的准确性,并在患者就诊期间提供检测结果。

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