Purpose: Vascular endothelial growth factor (VEGF) has been recognized as a
n important constituent of vascularization and growth of solid tumors. Seru
m VEGF levels were evaluated and correlated to clinicopathologic findings a
nd clinical outcome in patients with renal cell carcinoma (RCC).
Materials and Methods: Serum samples were collected before surgery in 164 p
atients with RCC. Levels of VEGF(165) protein in sera were measured using a
quantitative ELISA. Univariate and multivariate analyses were performed.
Results: The VEGF(165) level in serum was significantly increased (p = 0.00
01) in patients with RCC (median 343.4 pg./ml.) compared with the control p
atients (median 103.8 pg./ml.). The level of VEGF(165) in serum correlated
to clinical stage nd histopathological grade. Patients with VEGF(165) level
s below median value had significantly longer survival time than patients w
ith higher levels (p = 0.0001). This was also shown when VEGF(165) was anal
yzed in univariate Cox regression (p = 0.0001). The impact of VEGF(165) on
survival was especially shown in patients having tumors with vein invasion
(pT3b-c NO MO) and in patients with clinical stages I - III (p = 0.0240 and
p = 0.0023, respectively). When using multivariate analysis, only tumor st
age and grade remained as independent prognostic variables.
Conclusions: In RCC, serum VEGF(165) level was significantly correlated to
tumor stage and grade. Increased levels were correlated to adverse survival
. Although, VEGF did not remain as an independent prognostic factor in mult
ivariate analysis the levels of VEGF(165) in serum was found useful for the
identification of patients with potentially progressive disease especially
for those with vein invasion.