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Predictive Significance of VEGF and HIF-1α Expression in Patients with Metastatic Colorectal Cancer Receiving Chemotherapy Combinations with Bevacizumab

机译:VEGF和HIF-1α表达在转移结直肠癌接受化疗组合与Bevacizumab患者中的预测意义

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Background: There is no suggested molecular indicator for the determination of which patients will benefit from anti-angiogenetic treatment in metastatic colorectal cancers. Materials and Methods: In this study, VEGF and expression and their clinical significance were studied in tumor tissues of patients with colorectal cancer receiving bevacizumab-based treatment. VEGF and were assessed by immunohistochemistry in the primary tumors of 53 metastatic colorectal cancer patients receiving chemotherapy in combination with first line bevacizumab. Results: The clinical benefit rate in the low-VEGF expression group was 38%, while it was 62% in the high expression group. While the median progression-free survival (PFS) was 10 months in the high-VEGF expression group, it was 8 months in the low-VEGF expression group (p = 0.009). The median overall survival (OS) was found to be 26 months vs 15 months. Thus, when VEGF was strongly expressed it was in favor of that group and the difference was statistically significant (p = 0.03). High VEGF expression rate was an independent factor that correlated with OS or PFS (p=0.016 and 0.009, respectively). Conclusions: The data showed that VEGF may have predictive value for determining the treatment of CRC.
机译:背景:没有建议的分子指示剂测定哪些患者将从转移性结肠直肠癌中的抗血管生成治疗中受益。材料与方法:在本研究中,研究了VEGF和表达及其临床意义,并在接受基于Bevacizumab的患者患者的肿瘤组织中进行了临床意义。 VEGF并通过免疫组织化学在53个转移性结肠直肠癌患者接受化疗的主要肿瘤中评估,与第一线Bevacizumab组合。结果:低VEGF表达组的临床效益率为38%,高表达组为62%。虽然高VEGF表达组中位进展生存期(PFS)为10个月,但在低VEGF表达组中为8个月(p = 0.009)。中位数总存活(OS)被发现为26个月与15个月。因此,当VEGF强烈表达时,有利于该组,差异有统计学意义(P = 0.03)。高VEGF表达率是与OS或PFS相关的独立因素(分别为P = 0.016和0.009)。结论:数据显示VEGF可能具有确定CRC治疗的预测值。

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