BAGKGROUND. A clinical staging system based on the prostate-specific a
ntigen (PSA) and the calculated prostate carcinoma volume (cVCa) const
ruct previously has been proposed. This study was performed to assess
whether this proposed clinical staging system was valid in an independ
ent surgical and radiation data set in patients with clinically locali
zed disease. METHODS. Cox regression multivariable analyses were used
to assess the significance of staging systems (1992 American Joint Com
mission on Cancer Staging [AJCC] clinical and pathologic stage, versus
cVCa-PSA clinical stage) to predict time to posttherapy PSA failure i
n 441 and 465 patients managed by surgery and radiation, respectively.
Significant staging systems identified using Cox regression were test
ed further using established comparative measures to define the most c
linically useful system. RESULTS. Both the 1992 AJCC pathologic stage
and the cVCa-PSA clinical stage were significant predictors of time to
postoperative PSA failure (P = 0.0001), whereas only the cVCa-PSA cli
nical stage was a significant predictor of time to postradiation PSA f
ailure (P = 0.0001) using a Cox regression multivariable analysis. Fur
ther analyses using a pairwise comparison of the 1992 AJCC pathologic
stage and cVCa-PSA clinical stage found the cVCa-PSA staging system pr
ovided a more clinically useful prediction of time to postoperative PS
A failure. Specifically, the cVCa-PSA staging system was able to ident
ify surgically managed patients with pathologic AJCC T2 disease who di
d poorly (3-year bNED = 22%) while also selecting patients with clinic
al ATCC T2b,c disease that was managed by radiation who did well (3-ye
ar bNED = 100%). CONCLUSIONS. A clinical staging system based on param
eters obtained during the routine evaluation for AJCC clinical T1,2 pr
ostate carcinoma provided a clinically useful stratification of both p
ostoperative and postradiation PSA failure free survival. Cancer 1998;
83:2172-80. (C) 1998 American Cancer Society.