Clinical application of NMP22 in the management of transitional cell carcinoma of the bladder.

Cancer detection and prevention Pub Date : 2000-01-01
I S Sawczuk, E Bagiella, A T Sawczuk, E J Yun
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Abstract

The combination of a noninvasive, quantitative immunoassay, NMP22, with voided urinary cytology prior to cystoscopy was evaluated in patients with urothelial transitional cell carcinoma. Fifty-six patients with a history of transitional cell carcinoma were evaluated. Voided urine was obtained for NMP22 and cytology prior to cystoscopy. One hundred and twenty-three NMP22 assays, 124 cytologies, and 124 cystoscopies were performed. The type of anesthesia used for cystoscopic evaluation was determined by the NMP22 value in 30 patients. Cystoscopy results were considered positive on biopsy-confirmed malignancy. The reference value used for NMP22 was 10.0 U/ml. NMP22, cytology, and the combination of NMP22 and cytology were compared to cystoscopy and to pathologic grading and staging. Thirty-four recurrent transitional cell carcinoma episodes occurred; 22 were low-grade (I-II), and 12 were high-grade (III-IV). Twenty-seven were stage Ta; four were T1; and three were T3b or 4. Within this group, NMP22 detected low- and high-grade tumors equally, as compared to cytology, which was sensitive only to high-grade tumors. Nineteen patients were NMP22-negative and underwent cystoscopy under topical anesthesia; 17 were tumor-free. Eleven patients were NMP22-positive and had anesthesia, and all had visible lesions, which were subjected to biopsy and were resected. Six lesions were tumors, five were inflammatory. Overall sensitivity of combined NMP22 and cytology was 70%; specificity was 72%; positive predictive value was 54%; and negative predictive value was 77%. An accurate assessment of the risk of a bladder cancer can be obtained with NMP22, cytology, and cystoscopy in patients with a history of bladder cancer. NMP22 values can be used to determine the level of anesthesia for cystoscopy in patients with a history of bladder cancer.

NMP22在膀胱移行细胞癌治疗中的临床应用
在尿路上皮移行细胞癌患者中,非侵入性定量免疫测定NMP22与膀胱镜检查前尿细胞学检查相结合进行了评估。我们对56例有移行细胞癌病史的患者进行了评估。膀胱镜检查前取空尿进行NMP22和细胞学检查。进行了123例NMP22检测,124例细胞学检查和124例膀胱镜检查。根据30例患者的NMP22值确定用于膀胱镜评估的麻醉类型。膀胱镜检查结果被认为是阳性的活检证实的恶性肿瘤。NMP22的参考值为10.0 U/ml。将NMP22、细胞学检查以及NMP22与细胞学检查的结合与膀胱镜检查、病理分级和分期进行比较。34例移行细胞癌复发;低分级(I-II) 22例,高分级(III-IV) 12例。27个是第1阶段;4例T1;三个是T3b或4。在该组中,与细胞学相比,NMP22同样检测低级别和高级别肿瘤,而细胞学仅对高级别肿瘤敏感。19例患者nmp22阴性,在表面麻醉下行膀胱镜检查;17例无肿瘤。11例患者nmp22阳性且麻醉,均可见病变,行活检切除。6例为肿瘤,5例为炎症。NMP22与细胞学联合检测的总灵敏度为70%;特异性为72%;阳性预测值为54%;阴性预测值为77%。有膀胱癌病史的患者可以通过NMP22、细胞学检查和膀胱镜检查来准确评估膀胱癌的风险。NMP22值可用于判断膀胱癌病史患者膀胱镜麻醉水平。
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