ASSESSMENT OF OUTCOME PREDICTION MODELS FOR PATIENTS WITH LOCALIZED PROSTATE CARCINOMA MANAGED WITH RADICAL PROSTATECTOMY OR EXTERNAL-BEAM RADIATION-THERAPY
Av. Damico et al., ASSESSMENT OF OUTCOME PREDICTION MODELS FOR PATIENTS WITH LOCALIZED PROSTATE CARCINOMA MANAGED WITH RADICAL PROSTATECTOMY OR EXTERNAL-BEAM RADIATION-THERAPY, Cancer, 82(10), 1998, pp. 1887-1896
BACKGROUND. A clinical staging system for localized prostate carcinoma
that provides reliable information on which management decisions rega
rding an individual patient can be based is lacking. This study compar
ed the abilities of all published proposed clinical staging systems to
predict time to prostate specific antigen (PSA) failure after radical
prostatectomy or external beam radiation therapy for clinically local
ized prostate carcinoma. METHODS. A total of 1441 clinically localized
prostate carcinoma patients who were managed with radical prostatecto
my at the University of Pennsylvania in Philadelphia (n = 688) or the
Brigham and Women's Hospital in Boston (n = 288) or with external beam
radiation therapy at the Joint Center for Radiation Therapy in Boston
(n = 465) were entered into this study. Patients who received adjuvan
t or neoadjuvant hormonal or radiation therapy were excluded. Akaike's
Information Criterion (AIC) and Schwartz Bayesian Criterion (SBC) est
imates, which are comparative measures, were calculated for each clini
cal staging system. Pairwise comparisons of the AIC and SBC estimates
for the most predictive clinical staging systems were performed using
a formal bootstrap technique with 2000 replications. RESULTS. Both the
staging system based on the risk score and the staging system based o
n the calculated volume of prostate carcinoma and PSA (cV(Ca)-PSA) opt
imized the prediction of time to posttreatment PSA failure. The cV(Ca)
-PSA system, however, provided a more clinically useful stratification
of outcome. CONCLUSIONS. Improved clinical staging for patients with
localized prostate carcinoma may be possible with parameters obtained
during routine evaluation. Validation by other investigators is underw
ay. (C) 1998 American Cancer Society.