Background: The vascular endothelial growth factor (VEGF) is the angiogenic
growth factor most strongly implicated in tumor angiogenesis. Its special
role in the pathophysiology of ovarian cancer emerges from its dual functio
nal capability as an endothelial cell mitogen and a potent stimulator of va
scular permeability lending to the characteristic ascites accumulation in t
his disease. The aim of our study was to analyze the prognostic value of se
rum VEGF (sVEGF) as a tumor. marker in ovarian cancer. Patients and Methods
.. 41 patients with ovarian carcinomas were included in the study. Venous b
lood was taken from all patients preoperatively. From 15 patients an additi
onal postoperative blood sample was drawn. sVEGF was measured in duplicate
using a commercially available ELISA-kit. Results. The mean sVEGF level for
the ovarian cancer patients was 522 +/- 321 pg/ml (SD) (median: 440; range
: 55-1263 pg/ml) No statistically significant correlation could be found be
tween sVEGF concentrations and age, histologic type or FIGO-stage. sVEGF va
lues four week after surgery were significantly lower than those before tre
atment (p = 0.002). In patients after radical surgery sVEGF values dropped
or stayed stable below the cut-off more often than in patients with residua
l disease. In the univariate analysis, improved overall survival (OS) was f
ound for ovarian cancer patients with a sVEGF below the cut-off value of 44
0 pg/ml (p = 0.017). sVEGF was also tested in a multivariate analysis toget
her with residual disease and FIGO-stage using the Cox's proportional hazar
d model. In the final model only residual disease had nit independent influ
ence on OS (p = 0.018). Conclusion: sVEGF levels decrease significantly aft
er cytoreductive therapy and might indicate treatment efficiency. According
to our study, sVEGF is not an independent prognosticator of survival for o
varian cancer.