C. Maulard et al., SERUM TISSUE POLYPEPTIDE ANTIGEN (S-TPA) IN BLADDER-CANCER AS A TUMOR-MARKER - A PROSPECTIVE-STUDY, Cancer, 73(2), 1994, pp. 394-398
Background. Tissue polypeptide antigen (TPA) is a differentiation and
a proliferation tissue marker of nonsquamous epithelia. Increased urin
ary and serum TPA (S-TPA) levels were found in some patients with inva
sive bladder cancer. The authors report the results of a prospective s
tudy evaluating the role of serum TPA (S-TPA) in bladder carcinoma. Me
thods, S-TPA concentrations were measured by radioimmunoassay in 53 pa
tients with invasive bladder tumor before treatment, at the end of tre
atment, and during follow-up. The upper normal limit of the test was s
et at 80 UI/ml. Results. With a specificity of 100%, the diagnostic se
nsitivity of the test was 54.7%. S-TPA was increased in 88% of patient
s with N1 + N2 disease compared with 38.8% of the patients with N0 dis
ease (P = 0.01) and in 100% of patients with metastatic disease and 48
% of patients with nonmetastatic disease (P = 0.01). S-TPA was increas
ed in 23% of patients with total macroscopic debulking and in 68% of p
atients with persistent macroscopic disease (P = 0.004). For patients
staged N0 M0, no statistical correlation between S-TPA level and debul
king by transurethral resection (TUR) was found (P = 0.15). In the sub
set of patients with normal pretherapeutic S-TPA levels, 75% achieved
a complete response, compared with 44.8% of the patients with initial
elevated S-TPA levels (P = 0.04). However, there was no statistically
significant relationship between pretherapeutic S-TPA levels and immed
iate response to treatment according to the stratification for tumor v
olume after initial debulking by TUR. For a mean follow-up of 15 month
s +/- 7 months, median survival time and 1-year survival rates were st
udied in the subset of patients with limited disease (N0 M0) according
to the pretherapeutic S-TPA levels. The median survival time was not
reached, and the 1-year survival rate was 80% when the initial S-TPA l
evel was normal; these were 10 months and 44%, respectively, when the
S-TPA level was high (P < 0.01). Among the 31 patients who achieved a
complete response, 9 experienced a relapse, with an increase of the S-
TPA level in 8 patients. Conclusions. The S-TPA level is correlated wi
th initial tumor volume. It appears to be a prognostic factor and a va
luable parameter for follow-up.