
doi: 10.1007/bf02829566
pmid: 16961284
Circulating vascular endothelial growth factor-C (VEGF-C) and vascular endothelial growth factor (VEGF) levels in patients with colorectal carcinoma were determined in order to assess their clinical significance as a diagnostic tool for monitoring lymph node metastasis. In 66 patients with colorectal carcinoma and 30 healthy controls, circulating VEGF-C and VEGF levels were assessed by using enzyme-linked immunosorbent assay (ELISA). Serum VEGF-C and VEGF levels were higher in patients with colorectal carcinoma than in healthy controls. Patients with lymph node metastasis had higher serum VEGF-C and VEGF levels than those without lymph node metastasis. The levels of VEGF-C and VEGF were higher in the invasion group than in the non-invasion group. Serum VEGF-C levels reached a sensitivity of 81% and a specificity of 76% with a cutoff value of 1438.0 pg/mL, whereas VEGF levels reached 72% sensitivity and 74% specificity at 240.2 pg/ mL. If 66 patients were divided into 4 groups according to the combined determination of VEGF-C and VEGF levels, the positive predictive value was 85.3%, the negative predictive value was 94.6%, and accuracy was 93.7%. It was suggested that circulating VEGF-C levels might provide additional information for distinguishing the absence from presence of lymph node metastasis in patients with colorectal carcinoma. The combined determination of VEGF-C and VEGF levels could be used as an important index for preoperatively clinical stage of colorectal carcinoma.
Adult, Male, Vascular Endothelial Growth Factor A, Vascular Endothelial Growth Factor C, Enzyme-Linked Immunosorbent Assay, Adenocarcinoma, Middle Aged, Lymphatic Metastasis, Biomarkers, Tumor, Humans, Female, Neoplasm Invasiveness, Colorectal Neoplasms, Aged
Adult, Male, Vascular Endothelial Growth Factor A, Vascular Endothelial Growth Factor C, Enzyme-Linked Immunosorbent Assay, Adenocarcinoma, Middle Aged, Lymphatic Metastasis, Biomarkers, Tumor, Humans, Female, Neoplasm Invasiveness, Colorectal Neoplasms, Aged
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