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食管鳞状细胞癌中的肿瘤血管生成与预后

Tumor vascularization and prognosis in squamous cell carcinomas of the esophagus.

作者信息

Sarbia M, Bittinger F, Porschen R, Dutkowski P, Willers R, Gabbert H E

机构信息

Department of Pathology, Heinrich-Heine-University, Dusseldorf; Germany.

出版信息

Anticancer Res. 1996 Jul-Aug;16(4A):2117-21.

PMID:8712753
Abstract

Quantification of tumor vascularization has recently been shown to be a parameter of potential prognostic significance in various types of malignant tumors. To determine the prognostic value of tumor vascularization in esophageal cancer, tumor samples from 150 patients with squamous cell carcinoma of the esophagus and 10 samples of normal esophageal mucosa were stained immunohistochemically with the monoclonal antibody QBEND/10 (CD34), which recognises endothelial cells. Using light microscopy, the number of microvessels was counted in the areas with the highest microvessel density (MVD). The microvessel density was significantly higher in the normal esophageal mucosa (mean: 130/mm2) than in the tumor samples (mean: 69/mm2, p = 0.0001). Correlation of the MVD in the tumor tissue with other prognostic factors showed significantly lower microvessel counts in tumors with lymphatic-vessel invasion (p = 0.0076) and in high pT-stages (p = 0.0081). No significant correlation was found between the MVD and pN stage, tumor size, tumor grade, blood-vessel invasion and proliferative activity. In the univariate survival analysis no significant differences were found between poorly vascularized tumors and highly vascularized tumors. A Cox proportional hazard regression selected the parameters lymphatic-vessel invasion (p = 0.0001), pT stage (p = 0.0034) and pN stage (p = 0.0256) but not MVD as independent prognostic variables.

摘要

最近研究表明,肿瘤血管生成的定量分析是各类恶性肿瘤中一个具有潜在预后意义的参数。为了确定肿瘤血管生成在食管癌中的预后价值,对150例食管鳞状细胞癌患者的肿瘤样本以及10份正常食管黏膜样本进行免疫组织化学染色,使用识别内皮细胞的单克隆抗体QBEND/10(CD34)。通过光学显微镜,在微血管密度(MVD)最高的区域计数微血管数量。正常食管黏膜中的微血管密度(平均值:130/mm²)显著高于肿瘤样本(平均值:69/mm²,p = 0.0001)。肿瘤组织中的MVD与其他预后因素的相关性显示,有淋巴管侵犯的肿瘤(p = 0.0076)和高pT分期的肿瘤(p = 0.0081)微血管计数显著更低。未发现MVD与pN分期、肿瘤大小、肿瘤分级、血管侵犯及增殖活性之间存在显著相关性。在单因素生存分析中,血管生成少的肿瘤和血管生成多的肿瘤之间未发现显著差异。Cox比例风险回归分析选择淋巴管侵犯(p = 0.0001)、pT分期(p = 0.0034)和pN分期(p = 0.0256)作为独立预后变量,而未选择MVD。

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