F. Haab et al., CLEARANCE OF SERUM PSA AFTER OPEN SURGERY FOR BENIGN PROSTATIC HYPERTROPHY, RADICAL CYSTECTOMY, AND RADICAL PROSTATECTOMY, The Prostate, 26(6), 1995, pp. 334-338
Objective: To study the clearance of serum prostate-specific antigen (
PSA) after several types of prostatic tissue ablation. Methods: Serum
PSA levels were measured (YANG Proscheck ultrasensitive assay) just be
fore surgery, immediately after specimen removal, then twice weekly fo
r 5 weeks or until it was undetectable (<0.05 ng/ml) in patients under
going radical cystoprostatectomy for bladder cancer (n = 10), or radic
al prostatectomy for T1 T2 prostate cancer (n = 18) and daily for 6 da
ys after open surgery for benign prostatic hypertrophy (BPH) (n = 10).
Results: Open enucleation for BPH: the immediately postoperative PSA
level was 6 times its preoperative value. It decreased following a mon
oexponential curve with a very short half-life of 0.55 +/- 0.39 days,
range (0.14-1.3), reaching a value lower than the preoperative level i
n all cases, except one by day 3. After radical cystoprostatectomy: th
e decrease of serum PSA is monoexponential with a half life of 1.92 +/
- 1.2 days (0.57-4.24) reaching undetectable level (<0.05 ng/ml) in al
l patients by day 21. After radical prostatectomy: 11/18 patients (61%
) showed a one-component exponential decrease in PSA with a half-life
of 2.5 +/- 1.33 days (range 0.97-4.6 days), and 7/18 showed a two-comp
onent exponential decrease with a first half-life of 0.94 +/- 0.8 days
and a second of 7.62 +/- 6.35 days); 100% of the patients reached und
etectable serum PSA by day 28 in the first group compared to 14.2% of
the patients with a two component exponential decrease (P < 0.01). The
re was no difference between these groups as far as preoperative PSA l
evels and specimen pathology were concerned. Conclusion: Serum clearan
ce of PSA after extirpative prostatic surgery is closely related to th
e type and indication of procedure used. Radical cystoprostatectomy is
probably the best model in which to study the pharmacokinetics of PSA
. (C) 1995 Wiley-Liss, Inc.