BACKGROUND. Although glucocorticoids have been used to treat patients with
hormone-refractory prostate carcinoma (HRPC), reports have varied regarding
the types and doses of glucocorticoids used as well as their clinical bene
fits. In the current study, low doses of dexamethasone were investigated fo
r their specific beneficial effects and the feasibility of long term treatm
ent.
METHODS. Thirty-seven patients diagnosed with HRPC were treated with oral d
examethasone (0.5-2 mg/day). The patients ranged in age from 53-89 years (m
edian, 74 years]. Thirty-two patients, including 6 with lymph node metastas
es, had bone involvement whereas only 5 patients were found to have elevate
d serum prostate specific antigen (PSA) levels.
RESULTS. Twenty-three patients (62%) who received no other concomitant ther
apy demonstrated a decline in their serum PSA level of greater than or equa
l to 50%, which was confirmed by a second PSA value obtained greater than o
r equal to 4 weeks later. The median time to PSA progression was 9 months.
Among 18 patients with bone pain, 11 (61%) had improvement and in 5 patient
s (28%) the pain became stable. Among 21 patients with interpretable bone s
cans, 4 (19%) showed improvement and 8; (38%) achieved stable disease. Both
symptomatic and objective responses of bone metastases were correlated wit
h declines in the serum PSA level of greater than or equal to 50%. Ten pati
ents achieved an increase in their hemoglobin level of at least 2 g/dL. Pat
ients whose PSA level declined by greater than or equal to 50% with therapy
had significantly prolonged survival (median, 22 months). As pretreatment
markers, a longer interval before the initial evidence of-disease progressi
on appeared was found to correlate significantly with posttherapy PSA decli
nes of greater than or equal to 75%. All side effects of the glucocorticoid
s were reported to be mild.
CONCLUSIONS. Low doses of dexamethasone were found to be beneficial in the
treatment of HRPC, decreasing the severity of anemia and osseous disease as
well as reducing serum PSA levels. A posttherapy serum PSA decline of grea
ter than or equal to 50% appears to be a reliable marker of improved surviv
al with this therapy. Cancer 2000;89: 2570-6.. (C) 2000 American Cancer Soc
iety.