Pf. Schellhammer et al., PROSTATE-SPECIFIC ANTIGEN TO DETERMINE PROGRESSION-FREE SURVIVAL AFTER RADIATION-THERAPY FOR LOCALIZED CARCINOMA OF PROSTATE, Urology, 42(1), 1993, pp. 13-20
Prostate-specific antigen (PSA) levels after radiation therapy will mo
re precisely and objectively identify the presence of persistent prost
ate carcinoma. We determined the impact of PSA marker levels on progre
ssion-free status for 123 patients treated by interstitial implantatio
n (1-125) and 311 patients treated by external beam therapy (XRT) who
have been followed for a median of 109 and 51 months, respectively. Ac
tuarial progression-free survival curves were calculated, using standa
rd clinical criteria, and then recalculated, using PSA marker criteria
. Sera obtained twelve months or more after the initiation of XRT and
twenty-four months or more after the date of 1-125 were used for deter
mination of PSA levels. Using normal PSA level (by Hybritech assay les
s-than-or-equal-to 4.0 ng/mL) as the criterion for progression-free st
atus for patients treated by XRT, 35 percent of patients with Stage A2
, 20 percent of patients with Stage B1 or B2, and 10 percent of patien
ts with Stage C tumor were progression-free at ten years. The progress
ion-free survival by clinical criteria for Stage A2 was 65 percent, B1
was 40 percent, B2 was 35 percent, and C was 25 percent. Using undete
ctable PSA level (less-than-or-equal-to 0.5 ng/mL) as the criterion, l
ess than 10 percent of patients were progression-free at ten years, re
gardless of stage, grade; and treatment modality. This information sho
uld not be interpreted as indicating that radiation is ineffective the
rapy for prostate cancer, since clinical control of the disease among
men in their eighth decade is a more practical goal than marker contro
l. However, PSA monitoring after radiation therapy and after any local
therapy for prostate cancer will provide more precise information on
the success of that therapy in ablating disease.