Department of Internal Medicine, The University of New Mexico Cancer Center, Albuquerque, NM, USA.
BMC Cancer. 2012 Jul 19;12:298. doi: 10.1186/1471-2407-12-298.
Inflammatory breast cancer (IBC) is a highly angiogenic disease; thus, antiangiogenic therapy should result in a clinical response. However, clinical trials have demonstrated only modest responses, and the reasons for these outcomes remain unknown. Therefore, the purpose of this retrospective study was to determine the prognostic value of protein levels of vascular endothelial growth factor (VEGF-A), one of the main targets of antiangiogenic therapy, and its receptors (VEGF-R1 and -R2) in IBC tumor specimens.
Specimens from IBC and normal breast tissues were obtained from Algerian patients. Tumor epithelial and stromal staining of VEGF-A, VEGF-R1, and VEGF-R2 was evaluated by immunohistochemical analysis in tumors and normal breast tissues; this expression was correlated with clinicopathological variables and breast cancer-specific survival (BCSS) and disease-free survival (DFS) duration.
From a set of 117 IBC samples, we evaluated 103 ductal IBC tissues and 25 normal specimens. Significantly lower epithelial VEGF-A immunostaining was found in IBC tumor cells than in normal breast tissues (P <0.01), cytoplasmic VEGF-R1 and nuclear VEGF-R2 levels were slightly higher, and cytoplasmic VEGF-R2 levels were significantly higher (P = 0.04). Sixty-two percent of IBC tumors had high stromal VEGF-A expression. In univariate analysis, stromal VEGF-A levels predicted BCSS and DFS in IBC patients with estrogen receptor-positive (P <0.01 for both), progesterone receptor-positive (P = 0.04 and P = 0.03), HER2+ (P = 0.04 and P = 0.03), and lymph node involvement (P <0.01 for both). Strikingly, in a multivariate analysis, tumor stromal VEGF-A was identified as an independent predictor of poor BCSS (hazard ratio [HR]: 5.0; 95% CI: 2.0-12.3; P <0.01) and DFS (HR: 4.2; 95% CI: 1.7-10.3; P <0.01).
To our knowledge, this is the first study to demonstrate that tumor stromal VEGF-A expression is a valuable prognostic indicator of BCSS and DFS at diagnosis and can therefore be used to stratify IBC patients into low-risk and high-risk groups for death and relapses. High levels of tumor stromal VEGF-A may be useful for identifying IBC patients who will benefit from anti-angiogenic treatment.
炎性乳腺癌(IBC)是一种高度血管生成的疾病;因此,抗血管生成治疗应该会产生临床反应。然而,临床试验仅显示出适度的反应,这些结果的原因仍不清楚。因此,本回顾性研究的目的是确定血管内皮生长因子(VEGF-A)-一种抗血管生成治疗的主要靶点-及其受体(VEGF-R1 和 VEGF-R2)在 IBC 肿瘤标本中的蛋白水平的预后价值。
从阿尔及利亚患者中获得 IBC 和正常乳腺组织的标本。通过免疫组织化学分析评估 VEGF-A、VEGF-R1 和 VEGF-R2 在肿瘤和正常乳腺组织中的上皮和基质染色;这种表达与临床病理变量以及乳腺癌特异性生存(BCSS)和无病生存(DFS)时间相关。
从一组 117 例 IBC 样本中,我们评估了 103 例导管 IBC 组织和 25 例正常标本。与正常乳腺组织相比,IBC 肿瘤细胞中的上皮 VEGF-A 免疫染色明显较低(P <0.01),细胞质 VEGF-R1 和核 VEGF-R2 水平略高,细胞质 VEGF-R2 水平明显升高(P = 0.04)。62%的 IBC 肿瘤有高的基质 VEGF-A 表达。在单因素分析中,基质 VEGF-A 水平预测了雌激素受体阳性(P <0.01)、孕激素受体阳性(P = 0.04 和 P = 0.03)、HER2+(P = 0.04 和 P = 0.03)和淋巴结受累(P <0.01)的 IBC 患者的 BCSS 和 DFS。值得注意的是,在多因素分析中,肿瘤基质 VEGF-A 被确定为不良 BCSS(风险比[HR]:5.0;95%CI:2.0-12.3;P <0.01)和 DFS(HR:4.2;95%CI:1.7-10.3;P <0.01)的独立预测因子。
据我们所知,这是第一项表明肿瘤基质 VEGF-A 表达是诊断时 BCSS 和 DFS 的有价值的预后指标的研究,因此可以用于将 IBC 患者分为死亡和复发的低风险和高风险组。肿瘤基质 VEGF-A 水平较高可能有助于识别将从抗血管生成治疗中获益的 IBC 患者。