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Prognostic analysis of tumour angiogenesis determined by microvessel density and expression of vascular endothelial growth factor in high-risk primary breast cancer patients treated with high-dose chemotherapy

机译:由微血管密度和血管内皮生长因子表达确定的肿瘤血管生成的预后分析在高剂量化学疗法治疗的高危原发性乳腺癌患者中

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摘要

In contrast to early breast cancer, the prognostic effect of tumour angiogenesis in tumours with advanced axillary spread has been less studied. We retrospectively analysed the effect of microvessel density (MVD) and vascular endothelial growth factor (VEGF) by immunohistochemistry on the outcome of 215 patients treated uniformly within prospective trials of high-dose chemotherapy for 4–9 and ⩾10 positive nodes, and followed for a median of 9 (range 3–13) years. Microvessel density was associated with epidermal growth factor receptor (EGFR) expression (P<0.001) and tumour size (P=0.001). Vascular endothelial growth factor overexpression (51% of patients) was associated with overexpression of EGFR (P=0.01) and HER2 (P<0.05), but not with MVD (P=0.3). High MVD was associated with worse relapse-free survival (74 vs 44%, P<0.001) and overall survival (76 vs 44%, P<0.001). Vascular endothelial growth factor overexpression had no effect on outcome. Multivariate analyses showed a prognostic effect of MVD independently of other known prognostic factors in this patient population. In conclusion, tumour angiogenesis, expressed as MVD, is a major independent prognostic factor in breast cancer patients with extensive axillary involvement.
机译:与早期乳腺癌相反,在晚期腋窝扩散的肿瘤中,肿瘤血管生成的预后效应尚待研究。我们回顾性分析了免疫组织化学法对微血管密度(MVD)和血管内皮生长因子(VEGF)的影响,该研究对高剂量化疗4–9和⩾10阳性淋巴结前瞻性试验中统一治疗的215例患者的结果进行了随访,中位数为9年(范围3-13)。微血管密度与表皮生长因子受体(EGFR)表达(P <0.001)和肿瘤大小(P = 0.001)相关。血管内皮生长因子的过表达(占患者的51%)与EGFR(P = 0.01)和HER2(P <0.05)的过表达有关,而与MVD无关(P = 0.3)。高MVD与较差的无复发生存期(74 vs 44%,P <0.001)和总生存期(76 vs 44%,P <0.001)相关。血管内皮生长因子的过表达对结局没有影响。多变量分析显示了该患者人群中MVD的预后效果与其他已知预后因素无关。总之,表达为MVD的肿瘤血管生成是腋窝广泛受累的乳腺癌患者的主要独立预后因素。

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