Andersen Sigve, Donnem Tom, Al-Saad Samer, Al-Shibli Khalid, Busund Lill-Tove, Bremnes Roy M
Institute of Clinical Medicine, University of Tromso, Tromso, Norway.
J Thorac Oncol. 2009 Apr;4(4):463-71. doi: 10.1097/JTO.0b013e3181991d18.
Protein expressions of angiogenic markers provide prognostic information on patients with non-small cell lung cancer (NSCLC). Both expression and its prognostic impact may be associated with patient selection. Data addressing the prognostic relevance of angiogenic marker expression in NSCLC patients treated with postoperative radiotherapy (PORT) is warranted.
In 55 patients with stage I-IIIA NSCLC administered PORT between 1990 and 2005, we have reviewed the clinicopathological variables and investigated the expression of angiogenic markers in tumor and stroma in tissue micro arrays.
The median follow-up was 114 months and the major end point disease-specific survival (DSS). Univariate analysis showed that high expression of vascular endothelial growth factor A (VEGF-A) (p = 0.004), VEGF receptor-1 (VEGFR-1, p = 0.028), VEGFR-2 (p = 0.021), VEGFR-3 (p = 0.001) and platelet derived growth factor (PDGF) in tumors correlated significantly with a poor survival. Inversely, high basic fibroblast growth factor (bFGF) expression in stroma was associated with significantly improved DSS (p = 0.017). In multivariate analyses, tumor PDGF expression appeared independently associated with a shorter DSS (hazard ratio 5.42, p = 0.002) and stromal bFGF expression an increased DSS (hazard ratio 0.077, p < 0.001).
Tumor PDGF expression was an independent negative prognostic factor and stromal bFGF expression an independent positive prognostic factor for survival in NSCLC receiving PORT.
血管生成标志物的蛋白表达可为非小细胞肺癌(NSCLC)患者提供预后信息。其表达及其预后影响可能与患者选择有关。有必要提供关于接受术后放疗(PORT)的NSCLC患者血管生成标志物表达的预后相关性的数据。
在1990年至2005年间接受PORT的55例I-IIIA期NSCLC患者中,我们回顾了临床病理变量,并研究了组织微阵列中肿瘤和基质中血管生成标志物的表达。
中位随访时间为114个月,主要终点为疾病特异性生存(DSS)。单因素分析显示,肿瘤中血管内皮生长因子A(VEGF-A)高表达(p = 0.004)、血管内皮生长因子受体-1(VEGFR-1,p = 0.028)、VEGFR-2(p = 0.021)、VEGFR-3(p = 0.001)和血小板衍生生长因子(PDGF)与较差的生存率显著相关。相反,基质中碱性成纤维细胞生长因子(bFGF)高表达与DSS显著改善相关(p = 0.017)。多因素分析显示,肿瘤PDGF表达独立地与较短的DSS相关(风险比5.42,p = 0.002),而基质bFGF表达与DSS增加相关(风险比0.077,p < 0.001)。
在接受PORT的NSCLC患者中,肿瘤PDGF表达是生存的独立负性预后因素,而基质bFGF表达是独立的正性预后因素。