首页> 外文期刊>Urologic oncology >Surveillance for recurrent bladder cancer using a point-of-care proteomic assay Grossman HB, Soloway M, Messing E, Katz G, Stein B, Kassabian V, Shen Y, Department of Urology, M.D. Anderson Cancer Center, Houston, TX.
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Surveillance for recurrent bladder cancer using a point-of-care proteomic assay Grossman HB, Soloway M, Messing E, Katz G, Stein B, Kassabian V, Shen Y, Department of Urology, M.D. Anderson Cancer Center, Houston, TX.

机译:使用即时点蛋白质组学检测对复发性膀胱癌进行监测Grossman HB,Soloway M,Messing E,Katz G,Stein B,Kassabian V,Shen Y,马里兰州安德森癌症中心泌尿外科,德克萨斯州休斯顿。

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CONTEXT: At least 50% of patients with a history of bladder cancer have recurrences, so rigorous surveillance is necessary. Cystoscopy is standard but can fail to detect some bladder cancers, so a urine test is frequently part of the evaluation. OBJECTIVE: To investigate whether a point-of-care proteomic test that measures the nuclear matrix protein NMP22 in voided urine could improve detection of recurrence during monitoring of patients with a history of bladder cancer. DESIGN, SETTING, AND PATIENTS: From September 2001 to February 2002, 23 academic, private practice, and hospital facilities in 9 US states prospectively enrolled 668 consecutive patients with a history of bladder cancer in this cross-sectional study. Patients provided a voided urine sample for analysis of NMP22 protein and cytology prior to cystoscopy. MAIN OUTCOME MEASURES: Diagnosis of bladder cancer recurrence, 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 detection. Testing for the NMP22 tumor marker was conducted in a blinded manner. RESULTS: Bladder cancer was diagnosed in 103 patients. Cystoscopy alone identified 91.3% of the cancers (94/103; 95% confidence interval [CI], 84.1%-95.9%). The combination of cystoscopy with the NMP22 assay detected 99.0% of the malignancies (102/103; 95% CI, 94.7%-100%; P = .005). The NMP22 assay detected 8 of 9 cancers that were not visualized during initial cystoscopy, including 7 that were high-grade. The sensitivity and specificity of the NMP22 test alone were 49.5% (51/103; 95% CI, 39.5%-59.5%) and 87.3% (493/565; 95% CI, 84.2%-89.9%), respectively. Voided cytology detected only 3 of the malignancies missed during initial cystoscopy and did not significantly increase the sensitivity of cystoscopy (94.2%; 95% CI, 87.7%-97.8%; P = .08). CONCLUSION: The noninvasive point-of-care assay for elevated urinary NMP22 protein can increase the ability to detect recurrent bladder cancer, with test results available during the patient visit.
机译:背景:至少有50%的膀胱癌病史患者有复发,因此必须进行严格的监测。膀胱镜检查是标准的,但可能无法检测到某些膀胱癌,因此尿液检查经常是评估的一部分。目的:探讨一种在尿液中检测核基质蛋白NMP22的即时护理蛋白质组学测试能否改善监测膀胱癌病史患者的复发率。设计,地点和患者:从2001年9月到2002年2月,美国9个州的23个学术,私人执业和医院机构前瞻性地招募了668名患有膀胱癌病史的患者。患者在膀胱镜检查前提供了尿液样本,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复发诊断为参考标准。将NMP22测试的性能与无效尿细胞学检查进行比较,以帮助进行检测。 NMP22肿瘤标志物的测试以盲法进行。结果:103例患者被诊断出膀胱癌。仅通过膀胱镜检查就可以确定91.3%的癌症(94/103; 95%的置信区间[CI],84.1%-95.9%)。膀胱镜检查与NMP22检测相结合可检测出99.0%的恶性肿瘤(102/103; 95%CI,94.7%-100%; P = .005)。 NMP22测定法检测了在最初的膀胱镜检查中未发现的9种癌症中的8种,其中7种是高级别的。仅NMP22测试的敏感性和特异性分别为49.5%(51/103; 95%CI,39.5%-59.5%)和87.3%(493/565; 95%CI,84.2%-89.9%)。无效的细胞学检查仅检测到最初膀胱镜检查中漏诊的恶性肿瘤中的3个,并没有显着增加膀胱镜检查的敏感性(94.2%; 95%CI,87.7%-97.8%; P = 0.08)。结论:尿液中NMP22蛋白升高的非侵入性即时检测可以提高检测复发性膀胱癌的能力,在患者就诊期间可以得到检测结果。

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