Eighty-two patients with advanced prostatic carcinoma were treated wit
h a long-acting luteinizing hormone releasing hormone (LHRH) agonist (
Zoladex(R) depot, Zeneca Pharmaceuticals, England). The outcome of the
treatment was monitored on the basis of the following prognostic fact
ors: local stage, number of bone metastases, histological differentiat
ion grade and prostate-specific acid phosphatase (PAP), alkaline phosp
hatase (AF) and testosterone levels. The patients were followed-up unt
il disease progression or until death. The mean weight of the prostate
decreased from 48.1 g to 17.4 g (IJ < 0.00001) during the first year
of treatment. Statistically there was a significant difference in rega
rd to appearance of progression between different clinical stages (P <
0.00001). The prognosis was poorest in patients with more than 10 met
astases at the primary stage. If the PAP level was initially high (ove
r 20 mu g/L), the prognosis was very poor. Statistically there was a s
ignificant difference between the high PAP level and the slightly elev
ated or normal FAP (P < 0.02 and P < 0.005, respectively). Alkaline ph
osphatase (AF) appeared to be a good prognostic factor. The prognosis
was particularly poor, if the AF level exceeded 1000 U/L (P < 0.00001
and P < 0.05, compared with normal AF and slightly elevated AP level,
respectively). Surprisingly, a high pre-treatment testosterone level w
orsened the prognosis during the LHRH agonist treatment (P < 0.01, com
pared to patients with normal testosterone level). This is a new findi
ng and controversial to the findings reported before.