Background: Transitional cell carcinoma of the bladder (TCC) is the second
most common malignancy of the urinary tract. More than 70% of treated tumor
s recur, and 30% of recurrent tumors progress. Currently, pathologic stagin
g and grading are valuable prognostic factors for detecting and monitoring
TCC. Urinalysis, cystoscopy, and cytology are either invasive or lack sensi
tivity and specificity. The availability of a noninvasive, reliable, and si
mple test would greatly improve the detection and monitoring of patients wi
th TCC. Several biomarkers for bladder cancer have been proposed, but no si
ngle marker has emerged as the test of choice.
Approach: We undertook a comprehensive literature search using Medline to i
dentify all publications from 1980 to 1999. Articles that discussed potenti
al biomarkers for TCC were screened. Only compounds that demonstrated high
sensitivity or specificity, significant correlation with TCC diagnosis and
staging, and extensive investigation were included in this review.
Content: Potential biomarkers of disease progression and prognosis include
nuclear matrix protein, fibrin/fibrinogen product, bladder tumor antigen, b
lood group-related antigens, tumor-associated antigens, proliferating antig
ens, oncogenes, growth factors, cell adhesion molecules, and cell cycle reg
ulatory proteins. The properties of the biomarkers and the methods for dete
cting or quantifying; them are presented. Their sensitivities and specifici
ties for detecting and monitoring disease were 54-100% and 61-97%, respecti
vely, compared with 20-40% and 90% for urinalysis and cytology.
Summary: Although urine cytology and cystoscopy are still the standard of p
ractice, many candidate biomarkers for TCC are emerging and being adopted i
nto clinical practice. Further research and better understanding of the bio
logy of bladder cancer, improved diagnostic techniques, and standardized in
terpretation are essential steps to develop reliable biomarkers. It is poss
ible that using the current biomarkers as an adjuvant modality will improve
our ability to diagnose and monitor bladder cancer. (C) 2000 American Asso
ciation for Clinical Chemistry.