Teknos Theodoros N, Cox Claudell, Yoo Sirius, Chepeha Douglas B, Wolf Gregory T, Bradford Carol R, Carey Thomas E, Fisher Susan G
Department of Otolaryngology-Head and Neck Surgery, University of Michigan Health System, 1500 E Medical Center Dr, Ann Arbor, Michigan 48109-0312, USA.
Head Neck. 2002 Nov;24(11):1004-11. doi: 10.1002/hed.10163.
The purpose of this study was to determine whether serum vascular endothelial growth factor (s-VEGF) levels at the time of diagnosis correlate with any known tumor variables and overall survival in patients with advanced laryngeal squamous cell carcinoma. Comparisons with a cohort of normal healthy controls were also performed to determine the potential usefulness of s-VEGF as a screening tool.
Serum from patients enrolled in the VA Laryngeal Cooperative Study #258 (n = 183), as well as normal healthy controls (n = 40) was used in this analysis. Quantitative enzyme-linked immunosorbent assays (ELISA) for VEGF were performed in duplicate on each serum sample. Demographic and survival data were available for each patient enrolled in the study. Univariate analyses, multivariate Cox regression analyses, and Kaplan-Meier survival analysis were used.
The mean serum concentration of s-VEGF for the healthy control group was 47.83 +/- 0.13 pg/mL. For all patients enrolled in the VA Cooperative Study, regardless of treatment group, the mean s-VEGF level was 317.22 +/- 25.46 pg/mL. The patients randomly assigned to the surgical arm (n = 97) had a mean value of 315.44 +/- 30.44 pg/mL. Those randomly assigned to the induction chemotherapy arm (n = 86) had a mean s-VEGF level of 319.22 +/- 42.11 pg/mL. Serum VEGF levels were significantly elevated in patients with laryngeal carcinoma compared with healthy controls (p < .001). The serum VEGF levels in each arm of the trial were also elevated versus the healthy controls (p < .001, surgery arm plus radiotherapy; p < .001, chemotherapy plus radiotherapy). In a univariate analysis, elevated s-VEGF correlated with poor Karnofsky performance status for all patients with advanced laryngeal carcinoma (p < .008). High s-VEGF levels also correlated with a poor performance score in patients on the chemotherapy arm of the VA Laryngeal Trial (p < .004). Elevated s-VEGF levels in the surgical plus radiotherapy arm correlated with node-positive disease (p = .047) and supraglottic location of the tumor (p = .022). In a multivariate analysis using all known tumor variables and s-VEGF levels, elevated s-VEGF levels and infiltrating growth pattern correlated with decreased survival for all evaluated patients with advanced laryngeal carcinoma (p = .065, and p = .018, respectively).
Serum VEGF levels are significantly elevated in patients with advanced laryngeal carcinoma versus healthy controls. Elevated pretreatment s-VEGF levels tended to indicate a more aggressive disease state and a poorer overall survival in advanced laryngeal carcinoma.
本研究旨在确定晚期喉鳞状细胞癌患者诊断时血清血管内皮生长因子(s-VEGF)水平是否与任何已知肿瘤变量及总生存期相关。还与一组正常健康对照进行比较,以确定s-VEGF作为筛查工具的潜在用途。
本分析使用了参与退伍军人事务部喉癌合作研究#258的患者(n = 183)以及正常健康对照(n = 40)的血清。对每个血清样本进行了一式两份的VEGF定量酶联免疫吸附测定(ELISA)。可获取该研究中每位患者的人口统计学和生存数据。采用单因素分析、多因素Cox回归分析和Kaplan-Meier生存分析。
健康对照组的s-VEGF平均血清浓度为47.83±0.13 pg/mL。对于参与退伍军人事务部合作研究的所有患者,无论治疗组如何,s-VEGF平均水平为317.22±25.46 pg/mL。随机分配至手术组(n = 97)的患者平均值为315.44±30.44 pg/mL。随机分配至诱导化疗组(n = 86)的患者s-VEGF平均水平为319.22±42.11 pg/mL。与健康对照相比,喉癌患者的血清VEGF水平显著升高(p <.001)。试验各治疗组的血清VEGF水平与健康对照相比也升高(手术组加放疗,p <.001;化疗加放疗,p <.001)。在单因素分析中,s-VEGF升高与所有晚期喉癌患者较差的卡氏功能状态相关(p <.008)。在退伍军人事务部喉癌试验化疗组患者中,高s-VEGF水平也与较差的功能评分相关(p <.004)。手术加放疗组中s-VEGF水平升高与淋巴结阳性疾病(p =.047)和肿瘤声门上部位(p =.022)相关。在使用所有已知肿瘤变量和s-VEGF水平的多因素分析中,s-VEGF水平升高和浸润性生长模式与所有评估的晚期喉癌患者生存期缩短相关(分别为p =.065和p =.018)。
与健康对照相比,晚期喉癌患者的血清VEGF水平显著升高。治疗前s-VEGF水平升高往往表明晚期喉癌患者疾病状态更具侵袭性且总生存期更差。