Fernández Gómez Jesús M, García Rodríguez Jorge, Escaf Barmadah Safwan, Raigoso Pablo, Rodríguez Martínez Juan Javier, Allende María Teresa, Casasola Chamorro Javier, Rodríguez Faba Oscar, Martín Benito José Luis, Regadera Sejas Francisco Javier
Servicio de Urología, Hospital Central de Asturias, Facultad de Medicina, Universidad de Oviedo, Oviedo, Asturias, España.
Arch Esp Urol. 2002 Jan-Feb;55(1):41-9.
To determine the efficacy of urinary BTA-TRAK as a marker in monitoring superficial transitional cell carcinoma of the bladder and to compare urine cytology with urinary sediment testing.
700 consecutive determinations using BTA-TRAK to monitor unselected patients that had undergone surgery for transitional cell carcinoma of the bladder were analyzed. Cystoscopy, urinary sediment and urine cytology were performed during follow-up. Urography was performed yearly or when tumor of the upper urinary tract was suspected. (positive cytology or hematuria with no bladder tumor). Cystoscopy was performed a few days after determination of BTA-TRAK and voiding urine cytology and urinary sediment analyses (considered positive when microhematuria was observed) were both requested.
Of the 700 determinations, 95 (13.6%) were urothelial carcinomas (93 bladder, 2 upper urinary tract) that had been discovered during patient monitoring. Of the 93 bladder tumors, 39 were Ta (37 TaG1 and 2 TaG2), 29 T1 (4 T1G1, 20 T1G2 and 5 T1G3), 5 Tis and 20 muscle-infiltrating tumors (progression from T2-4 during monitoring). The sensitivity of urine cytology to detect urothelial tumor was 41.1% and the specificity was 97.3%. The urine cytologies were negative in 48.4% and inflammatory in 9.5% of the tumors. The sensitivity was 19% in low grade tumors. The sensitivity of urinary sedimentation testing to detect urothelial tumor (microhematuria) was 40% and the specificity was 96.7%. When associated with pyuria, it was considered to be a urinary infection or urothelial inflammatory condition, which was observed in 10.6% of the cases. Considering the proposed normal reference value for BTA-TRAK (< or = 14 U/ml), we have found a sensitivity of 62.1% and a specificity of 68.4%. A logistic regression model was developed, including BTA-TRAK, urinary sedimentation and cytology, to identify the independent variables that are useful for tumor detection during follow-up of superficial carcinoma of the bladder in this series. The combination of three variables showed an odds ratio of 18.5 (8.9-38.5) for urinary cytology, 11.8 (5.9-23.5) for urinary sedimentation and an odds ratio for BTA-TRAK that did not fall within the equation.
Although overall the sensitivity of BTA-TRAK is higher than that of urine cytology and urinary sedimentation testing, it provides no additional information than that obtained from the combination of urine cytology and urinary sedimentation testing in the detection of tumor recurrence during monitoring for superficial bladder cancer.
确定尿BTA-TRAK作为监测膀胱浅表性移行细胞癌标志物的疗效,并比较尿液细胞学检查与尿沉渣检测。
分析连续700次使用BTA-TRAK监测未经选择的膀胱移行细胞癌手术患者的结果。随访期间进行膀胱镜检查、尿沉渣和尿液细胞学检查。每年或怀疑上尿路肿瘤(阳性细胞学检查或血尿但无膀胱肿瘤)时进行尿路造影。在测定BTA-TRAK几天后进行膀胱镜检查,并要求进行排尿尿液细胞学检查和尿沉渣分析(当观察到微量血尿时视为阳性)。
在700次测定中,95次(13.6%)为在患者监测期间发现的尿路上皮癌(93例膀胱,2例上尿路)。在93例膀胱肿瘤中,39例为Ta期(37例TaG1和2例TaG2),29例为T1期(4例T1G1、20例T1G2和5例T1G3),5例为Tis期,20例为肌层浸润性肿瘤(监测期间从T2-4期进展而来)。尿液细胞学检查检测尿路上皮肿瘤的敏感性为41.1%,特异性为97.3%。48.4%的肿瘤尿液细胞学检查为阴性,9.5%为炎症性。低级别肿瘤的敏感性为19%。尿沉渣检测检测尿路上皮肿瘤(微量血尿)的敏感性为40%,特异性为96.7%。当伴有脓尿时,被认为是泌尿系统感染或尿路上皮炎症状态,在10.6%的病例中观察到。考虑到BTA-TRAK的建议正常参考值(≤14 U/ml),我们发现敏感性为62.1%,特异性为68.4%。建立了一个逻辑回归模型,包括BTA-TRAK、尿沉渣和细胞学检查,以确定在本系列膀胱浅表癌随访期间对肿瘤检测有用的独立变量。三个变量的组合显示,尿液细胞学检查的优势比为18.5(8.9-38.5),尿沉渣检查为11.8(5.9-23.5),BTA-TRAK的优势比未纳入该方程。
虽然总体而言,BTA-TRAK的敏感性高于尿液细胞学检查和尿沉渣检测,但在监测浅表性膀胱癌期间检测肿瘤复发方面,它并没有提供比尿液细胞学检查和尿沉渣检测组合更多的信息。