BACKGROUND. Serum TPS (tissue polypeptide-specific antigen) has been o
bserved to be characteristic of carcinoma proliferation, and increased
levels of TPS seem to be closely related to tumor progression. In thi
s study we wanted to evaluate the importance of the tumor-marker TPS i
n the diagnosis and follow-up of patients with prostatic carcinoma, an
d to compare it with prostate-specific antigen (PSA). METHODS. We cons
idered 39 patients with clinically confined disease, who underwent neo
adjuvant hormonal therapy and thereafter radical prostatectomy, and 45
patients who did not undergo surgery and underwent hormonal adjuvant
therapy alone. PSA and TPS were measured at the time of diagnosis and
at regular intervals in the follow-up; TPS was measured in a control g
roup of patients as well. RESULTS. We were able to observe that, in un
treated patients, PSA correlates with clinical stage, increasing with
increasing tumor stage; a similar correlation was not observed when co
nsidering TPS. After androgen ablation we observed a decrease in PSA,
but the serum values of TPS remained higher, suggesting that activity
still exists inside the tumor. The evaluation of TPS appeared to be of
particular interest in the follow-up after radical prostatectomy, esp
ecially in patients undergoing hormonal therapy; in fact, we were able
to observe that relapse of the disease can be suspected early by the
increase of TPS in hormonally treated patients. CONCLUSIONS. We assert
that TPS can add useful information on the state of neoplastic illnes
s, especially in patients following adjuvant androgen-suppressive horm
onal therapy, after radical prostatectomy; serial measurements of this
marker could be useful in the early diagnosis of a relapse. (C) 1997
Wiley-Liss, Inc.