Lentsch Eric J, Goudy Steven, Sosnowski Jeffrey, Major Scott, Bumpous Jeffrey M
Department of Surgery, Division of Otolaryngology-Head and Neck Surgery, University of Louisville School of Medicine, and the James Graham Brown Cancer Center, Louisville, Kentucky 40292, USA.
Laryngoscope. 2006 Mar;116(3):397-400. doi: 10.1097/01.MLG.0000195286.29613.E1.
Our objective was to assess angiogenesis in head and neck squamous cell primary tumors and measure its correlation with tumor site and clinical and pathologic staging parameters.
Patients from the tumor registries of the University of Louisville and affiliated hospitals who had biopsy-proven head and neck squamous cell carcinoma were retrospectively assessed over a 5-year period (1995-2000).
Patient records were reviewed for tumor site, TNM staging, surgical treatment, and tumor pathologic staging data. Cell blocks were obtained for each of the study patients, and CD31 staining was used to measure microvessel density (MVD) in areas of primary tumor hot spots.
Twenty-eight consecutive patients met inclusion criteria and had adequate cell blocks for evaluation. MVD for T3 staged (41.2 MVD, mean) and T4 staged (36.4 MVD, mean) tumors were higher than earlier staged T1 staged (31.3 MVD, mean) and T2 staged (24.9 MVD, mean) tumors. Laryngeal T3 and T4 tumors had MVDs as high as 43.4 MVD (mean) and 40.4 MVD (mean), respectively, compared with a 23.9 MVD for T2 tumors. This difference was statistically significant (P < .01). Our report indicates a trend toward increasing MVD with N-stage.
Our series demonstrates that there is a strong correlation between MVD in primary tumor hot spots and tumor T-stage, which implies that tumor angiogenesis may be a factor in tumor progression.
我们的目的是评估头颈部鳞状细胞原发性肿瘤中的血管生成情况,并测量其与肿瘤部位、临床和病理分期参数的相关性。
对来自路易斯维尔大学肿瘤登记处及附属医院的、经活检证实患有头颈部鳞状细胞癌的患者进行了为期5年(1995 - 2000年)的回顾性评估。
查阅患者记录,获取肿瘤部位、TNM分期、手术治疗及肿瘤病理分期数据。为每位研究患者获取细胞块,采用CD31染色测量原发性肿瘤热点区域的微血管密度(MVD)。
连续28例患者符合纳入标准且有足够的细胞块用于评估。T3期肿瘤(平均MVD为41.2)和T4期肿瘤(平均MVD为36.4)的MVD高于早期的T1期肿瘤(平均MVD为31.3)和T2期肿瘤(平均MVD为24.9)。喉T3和T4期肿瘤的MVD分别高达43.4(平均)和40.4(平均),而T2期肿瘤为23.9。这种差异具有统计学意义(P < .01)。我们的报告表明MVD有随N分期增加的趋势。
我们的系列研究表明,原发性肿瘤热点区域的MVD与肿瘤T分期之间存在很强的相关性,这意味着肿瘤血管生成可能是肿瘤进展的一个因素。