Context Dysregulation of apoptosis may favor onset and progression of cance
r and influence response to therapy. Survivin is an inhibitor of apoptosis
that is selectively overexpressed in common human cancers, but not in norma
l tissues, and that correlates with aggressive disease and unfavorable outc
omes,
Objective To investigate the potential suitability of survivin detection in
urine as a novel predictive/prognostic molecular marker of bladder cancer,
Design, Setting, and Patients Survey of urine specimens from 5 groups: heal
thy volunteers (n=17) and patients with nonneoplastic urinary tract disease
(n=30), genitourinary cancer (n=30), new-onset or recurrent bladder cancer
(n=46), or treated bladder cancer (n=35), recruited from 2 New England uro
logy clinics.
Main Outcome Measures Detectable survivin levels, analyzed by a novel detec
tion system and confirmed by Western blot and reverse transcriptase polymer
ase chain reaction (RT-PCR), in urine samples of the 5 participant groups.
Results Survivin was detected in the urine samples of all 46 patients with
new or recurrent bladder cancer using a novel detection system (31 of 31) a
nd RT-PCR (15 of ? 5) methods. Survivin was not detected in the urine sampl
es of 32 of 35 patients treated for bladder cancer and having negative cyst
oscopy results. None of the healthy volunteers or patients with prostate, k
idney, vaginal, or cervical cancer had detectable survivin in urine samples
, Of the 30 patients with nonneoplastic urinary tract disease, survivin was
detected in 3 patients who had bladder abnormalities noted using cystoscop
y and in 1 patient with an increased prostate-specific antigen level. Patie
nts with low-grade bladder cancer had significantly lower urine survivin le
vels than patients with carcinoma in situ (P=.002).
Conclusions Highly sensitive and specific determination of urine survivin a
ppears to provide a simple, noninvasive diagnostic test to identify patient
s with new or recurrent bladder cancer.