Tamura Masaya, Oda Makoto, Matsumoto Isao, Tsunezuka Yoshio, Kawakami Kazuyuki, Ohta Yasuhiko, Watanabe Go
Department of General and Cardiothoracic Surgery, Kanazawa University School of Medicine, Takara-machi 13-1, Ishikawa, Kanazawa 920-8641, Japan.
Ann Surg Oncol. 2004 Oct;11(10):928-33. doi: 10.1245/ASO.2004.01.013. Epub 2004 Sep 20.
The aim of the present study was to evaluate the diagnostic utility of levels of circulating vascular endothelial growth factor (VEGF)-C, matrix metalloproteinase-9 (MMP-9), and VEGF and to verify that the combination assay of these circulating factors is a clinically useful indicator to predict the presence of lymph node metastasis in non-small cell lung cancer (NSCLC).
A series of 78 patients who underwent surgery for NSCLC was used in this study. Serum VEGF-C and VEGF and plasma MMP-9 levels were analyzed with enzyme-linked immunosorbent assay (ELISA) kits. Logistic regression models were used to analyze the influence of VEGF-C, MMP, and VEGF levels on the probability of presence or absence of lymph node metastasis.
Patients with lymph node metastasis had higher serum VEGF- C, VEGF, and plasma MMP-9 concentrations than did those without metastasis (VEGF-C, P = .0004; VEGF, P = .001). Serum VEGF- C reached a sensitivity of 85% and specificity of 68% when a cutoff value of 1762.0 pg/mL was applied, while VEGF reached 80% sensitivity and 59% specificity at 316.8 pg/mL. MMP-9 reached a sensitivity of 63% and specificity of 75% when a cutoff value of 51.4 ng/mL was applied. In the ROC curve analysis, VEGF-C (0.761) had the biggest areas under the ROC curve, followed by MMP-9 (0.723) and VEGF (0.694). Combination assay of three markers had higher sensitivity and specificity for prediction than single-marker assays (AUC = 0.837).
This study has confirmed that combination assay of three markers to determine VEGF-C, MMP-9, and VEGF expression in circulation detects lymph node metastasis in NSCLC with higher accuracy than single-marker assays.
本研究旨在评估循环血管内皮生长因子(VEGF)-C、基质金属蛋白酶-9(MMP-9)和VEGF水平的诊断效用,并验证这些循环因子的联合检测是否为预测非小细胞肺癌(NSCLC)淋巴结转移的临床有用指标。
本研究纳入了78例行NSCLC手术的患者。采用酶联免疫吸附测定(ELISA)试剂盒分析血清VEGF-C、VEGF和血浆MMP-9水平。使用逻辑回归模型分析VEGF-C、MMP和VEGF水平对有无淋巴结转移概率的影响。
有淋巴结转移的患者血清VEGF-C、VEGF和血浆MMP-9浓度高于无转移患者(VEGF-C,P = 0.0004;VEGF,P = 0.001)。当应用1762.0 pg/mL的临界值时,血清VEGF-C的敏感性达到85%,特异性达到68%,而VEGF在316.8 pg/mL时敏感性达到80%,特异性达到59%。当应用51.4 ng/mL的临界值时,MMP-9的敏感性达到63%,特异性达到75%。在ROC曲线分析中,VEGF-C(0.761)的ROC曲线下面积最大,其次是MMP-9(0.723)和VEGF(0.694)。三种标志物的联合检测对预测的敏感性和特异性高于单一标志物检测(AUC = 0.837)。
本研究证实,联合检测三种标志物以确定循环中VEGF-C、MMP-9和VEGF的表达,检测NSCLC淋巴结转移的准确性高于单一标志物检测。