Tsihlias J, Grossman H B
Department of Urology, University of Texas M. D. Anderson Cancer Center, Houston, USA.
Urol Clin North Am. 2000 Feb;27(1):39-46. doi: 10.1016/s0094-0143(05)70232-9.
Fibrin/fibrinogen degradation products are either absent or present at exceedingly low levels in the urine of healthy persons. Although various nonspecific inflammatory conditions of the urinary tract can result in detectable amounts of FDP in the urine, the presence of FDP is far more prevalent in urine from patients with bladder cancer. Urinary FDP levels tend to be higher in patients with tumors of increasing grade and stage. This correlation results in improved sensitivity in detecting more aggressive tumors. Current monoclonal antibody immunoassays are simple, rapid, and inexpensive, and can be performed on urine samples in the clinical setting. The overall accuracy of these immunoassays ranges from 75% to 80% (Table 1), suggesting that the urine FDP test should not be used alone for the surveillance of superficial bladder cancer. When assays for urine FDP are combined with urine cytology, the sensitivity for detecting tumors is improved. Prospective data are needed to determine whether using these tests in combination can safely permit a reduced frequency of endoscopic surveillance.
在健康人的尿液中,纤维蛋白/纤维蛋白原降解产物(FDP)要么不存在,要么含量极低。虽然尿路的各种非特异性炎症状况可导致尿液中出现可检测量的FDP,但FDP在膀胱癌患者尿液中更为常见。随着肿瘤分级和分期的增加,膀胱癌患者的尿FDP水平往往更高。这种相关性提高了检测侵袭性更强肿瘤的敏感性。目前的单克隆抗体免疫测定法简单、快速且成本低廉,可在临床环境中对尿液样本进行检测。这些免疫测定法的总体准确率在75%至80%之间(表1),这表明尿FDP检测不应单独用于浅表性膀胱癌的监测。当尿FDP检测与尿细胞学检查相结合时,检测肿瘤的敏感性会提高。需要前瞻性数据来确定联合使用这些检测是否能安全地减少内镜监测的频率。