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UROLOGICAL
ONCOLOGY
Radiotherapy for men with isolated increase in serum prostate
specific antigen after radical prostatectomy
Macdonald OK, Schild SE, Vora SA, Andrews PE, Ferrigni RG, Novicki DE,
Swanson SK, Wong WW
Department of Radiation Oncology, Section of Urology, Mayo Clinic Scottsdale,
13400 E. Shea Boulevard, Scottsdale, AZ, 85259, USA
J Urol. 2003; 170: 1833-7
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Purpose:
In this retrospective study we determined the results of salvage external
beam radiation therapy (RT) to the prostate bed for isolated increase
of serum prostate specific antigen (PSA) after radical prostatectomy.
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Materials and Methods:
A total of 60 patients underwent RT for PSA failure after radical prostatectomy
from 1993 to 1999. Median followup was 51 months. Biochemical disease-free
survival (bDFS) with a serum PSA of 0.3 ng/mL or less was estimated
using the Kaplan-Meier method. Potential prognostic factors were evaluated
for significant associations with bDFS.
- Results:
Median PSA before RT was 0.69 ng/ml. Median radiation dose was 64.8
Gy. The 5-year actuarial bDFS was 45%. There were 32 patients with a
minimum followup of 4 years (median 73 months) who experienced a 5-year
bDFS rate of 43%. PSA before RT (p = 0.016), RT dose (p = 0.026), surgical
margin involvement (p = 0.017) and Gleason score (p = 0.018) were identified
as prognostic factors for bDFS. A significant association with bDFS
was present at 5 years of 65%, 34% and 0% for PSA before RT less than
0.6, 0.6 to 1.2, and greater than 1.2 ng/ml, respectively (p = 0.036).
Patients with PSA before RT less than 0.6 ng/ml and total RT dose greater
than 64.8 Gy had improved bDFS at 5 years compared to all others (77%
vs. 32%, p = 0.04). Of 60 patients 3 (5%) experienced chronic grade
3 toxicity.
- Conclusions:
Optimal benefit from salvage RT was achieved in patients with a PSA
less than 0.6 ng/ml and doses of RT greater than 64.8 Gy. Early treatment
with a sufficiently high dose of RT maximizes the potential for salvage.
- Editorial
Comment
This paper defines the timing and indication for adjuvant radiotherapy
after biochemical tumor recurrences following radical prostatectomy.
In conclusion, patients do better if treated at an PSA below 0.69 ng/ml,
with a local dose of at least 64.8 Gy, with Gleason scores below 7,
and, interestingly, with positive surgical margins. A possible explanation
for the letter fact is that patients with positive surgical margins
have a higher likelihood of localized microscopic residual disease in
the prostate bed. An increasing PSA would more easily indicate local
progression of that microscopic disease, whereas increasing PSA in the
margin negative group may indicate undetectable distant disease that
would not be treated effectively with radiotherapy to the prostate bed.
Altogether the results support an earlier the better approach to postoperative
radiotherapy.
Dr.
Andreas Böhle
Professor of Urology
HELIOS Agnes Karll Hospital
Bad Schwartau, Germany
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