Utility of serial urinary tumor markers to individualize intervals betweencystoscopies in the monitoring of patients with bladder carcinoma

Citation
M. Sanchez-carbayo et al., Utility of serial urinary tumor markers to individualize intervals betweencystoscopies in the monitoring of patients with bladder carcinoma, CANCER, 92(11), 2001, pp. 2820-2828
Citations number
30
Categorie Soggetti
Oncology,"Onconogenesis & Cancer Research
Journal title
CANCER
ISSN journal
0008543X → ACNP
Volume
92
Issue
11
Year of publication
2001
Pages
2820 - 2828
Database
ISI
SICI code
0008-543X(200112)92:11<2820:UOSUTM>2.0.ZU;2-5
Abstract
BACKGROUND. Cross-section studies have shown the diagnostic characteristics of certain urinary tumor markers for the detection of bladder carcinoma. H owever, the role of serial urinary tumor markers in the monitoring of patie nts with bladder carcinoma in daily clinical surveillance has not been comp letely defined yet. METHODS. The study comprised 1185 urine samples belonging to 232 patients w ith a previous bladder carcinoma: 106 patients under follow-up (Group 1) an d 126 bladder carcinoma patients receiving intravesic instillations (Group 2). Patients were monitored with urinary tumor markers during a one-year fo llow-up period. Urine samples were collected before cystoscopies and in the intercystoscopic periods for patients in Group 1 and before intravesic ins tillations for patients Group 2. Urinary bladder carcinoma antigen (UBC), C YFRA 21-1 and nuclear matrix proteins (NMP22) were measured by immunoassays . RESULTS. Monitoring of the disease with urinary tumor markers could detect recurrence sooner than scheduled cystoscopies in 27 patients (87%) for UBC, 27 patients (87%) for CYFRA 21-1, and 26 patients (84%) for NMP22 out of 3 1 Group 1 patients who recurred; and in 16 patients (67%) for UBC, 17 patie nts (71%) for cytokeratin fragments (CYFRA) 21-1, and 13 patients (54%) for NMP22 out of 24 Group 2 patients who recurred. The most relevant finding w as that persistence of negative urinary markers during follow-up was largel y indicative of disease free status in 65 of 75 (87%) patients of Group 1 a nd 31 of 102 (30%) cases of Group 2. Although false positive results were p resent, they Were mainly associated with sporadic urinary tract infections in 10 of 75 (13%) cases of Group 1 and in 36 of 102 (35%) patients of Group 2; and with urine samples collected in the first two months at the beginni ng of intravesic therapy in 35 of 102 patients (34%) in Group 2. CONCLUSIONS. Monitoring of bladder carcinoma patients with serial urinary t umor markers could anticipate detection of recurrence. Persistent negative results might postpone and reduce the number of cystoscopies. Once the limi tations leading to false positive results are controlled by urinalysis and by starting sample collection when basal levels are reached in patients wit h intravesic therapy, urinary tumor markers might eventually individualize the intervals between cystoscopies in the surveillance of patients with bla dder carcinoma. Cancer 2001;92:2820-8. (C) 2001 American Cancer Society.