Gd. Grossfeld et al., Intermittent androgen deprivation: Update of cycling characteristics in patients without clinically apparent metastatic prostate cancer, UROLOGY, 58(2), 2001, pp. 240-245
Objectives. To update the cycling characteristics and patterns of treatment
in patients receiving intermittent androgen deprivation (IAD) for clinical
ly localized and recurrent prostate cancer.
Methods. We report our experience with 61 patients treated with IAD. Thirty
-four patients had received no prior treatment, and 27 had developed recurr
ent disease after previous local therapy. No patient had clinically apparen
t metastatic disease before the initiation of therapy. The mean and median
serum prostate-specific antigen (PSA) level before treatment was 25.3 ng/mL
and 16.0 ng/mL, respectively (range 0.5 to 190 ng/mL). For each cycle, and
rogen deprivation was continued until PSA became undetectable or a nadir le
vel was reached. Patients were then observed without treatment, and therapy
was reinstituted after the serum PSA value reached a predetermined level.
Patients were no longer eligible to cycle off treatment when their serum PS
A increased despite ongoing androgen deprivation or if any objective eviden
ce of disease progression was present on imaging studies.
Results. Follow-up ranged from 7 to 60 months (mean 30) from the start of t
reatment. Patients received from one to five treatment cycles (median two),
with a median cycle length of 14 months. The median nadir serum PSA level
during androgen deprivation was 0.01 ng/mL and was reached within an averag
e of 6 months (range 4 to 9) after beginning treatment. Patients spent an a
verage of 45% of the time not receiving therapy, but the time off therapy d
ecreased as the number of treatment cycles increased. Five patients (8.1%)
demonstrated progressive disease, with a median time to progression of 48 m
onths. When examining the cycling characteristics of these patients, no con
sistent pattern of failure emerged.
Conclusions. IAD appears to be a viable treatment option in select patients
with localized prostate cancer. With each consecutive cycle, the amount of
time the patient was not receiving therapy decreased, despite achieving a
low nadir PSA. Longer follow-up with more patients failing IAD will be requ
ired before clear patterns of failure emerge in these patients. UROLOGY 58:
240-245, 2001. (C) 2001, Elsevier Science Inc.