Abstract
Tumor angiogenesis has been found to have prognostic significance in many tumor types for predicting an increased risk of metastasis. We assessed tumor vascularity in 43 cases of advanced stage (International Federation of Gynecologists and Obstetricians stages III and IV) ovarian cancer by using the highly specific endothelial cell marker CD34. Microvessel counts and stage were associated with disease-free survival and with overall survival by Kaplan-Meier analysis. The plots show that higher stage, higher average vessel count at 200x (200x avg) and 400x (400x avg) magnification and highest vessel count at 400x (400x high) magnification confer a worse prognosis for disease-free survival. Average vessel count of less than 16 (400x avg, P2 = 0.01) and less than 45 (200x avg, P2 = 0.026) suggested a better survival. Similarly, a high vessel count of less than 20 (400x high, P2 = 0.019) conferred a better survival as well. The plots suggest that higher stage, higher average vessel count at 200x and 400x, and highest vessel count at 200x and 400x show a trend to worse overall survival as well. With the Cox proportional hazards model, stage was the best predictor of overall survival, however, the average microvessel count at 400x was found to be the best predictor of disease-free survival. These results suggest that analysis of neovascularization in advanced stage ovarian cancer may be a useful prognostic factor.
MeSH Terms
Adolescent
Adult
Aged
Antigens, CD/analysis
Antigens, CD34
Biomarkers, Tumor
Capillaries/chemistry,pathology
Carcinoma/blood supply,chemistry,pathology
Cell Count
Disease-Free Survival
Endothelium, Vascular/chemistry,pathology
Female
Humans
Immunoenzyme Techniques
Middle Aged
Neoplasm Metastasis
Neoplasm Staging
Neovascularization, Pathologic/pathology
Ovarian Neoplasms/blood supply,chemistry,pathology
Prognosis
Proportional Hazards Models
Retrospective Studies
Survival Analysis
Chemicals
Antigens, CD
Antigens, CD34
Biomarkers, Tumor
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Hollingsworth H C
Laboratory of Pathology and Biostatistics, National Cancer Institute, Bethesda, Maryland 20892, USA.
Kohn E C
Steinberg S M
Rothenberg M L
Merino M J
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