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循环表皮生长因子样结构域 7 在化疗联合贝伐珠单抗治疗转移性结直肠癌患者中的预后意义。

Prognostic importance of circulating epidermal growth factor-like domain 7 in patients with metastatic colorectal cancer treated with chemotherapy and bevacizumab.

机构信息

Danish Colorectal Cancer Center South, Vejle Hospital, Institute of Regional Health Research, University of Southern Denmark, Odense, Denmark.

出版信息

Sci Rep. 2017 May 24;7(1):2388. doi: 10.1038/s41598-017-02538-x.

Abstract

High tumor expression of epidermal growth factor-like domain 7 (EGFL7) has been associated with a poor prognosis in colorectal cancer. The aim of the current study was to investigate the possible prognostic impact of circulating EGFL7 (cir-EGFL7), combined with single nucleotide polymorphism (SNP) analyses, in patients with metastatic colorectal cancer (mCRC) treated with first line chemotherapy and bevacizumab. A total of 88 patients were included. Serum was collected prior to treatment initiation, at first evaluation after 3 weeks, and at progression. Cir-EGFL7 was analysed by the enzyme-linked immunosorbent assay (ELISA) technique. The SNPs were analysed by real-time qPCR based on DNA from whole blood. Endpoints were response rate (RR), progression free survival (PFS), and overall survival (OS). Cir-EGFL7 decreases after administration of chemotherapy plus bevacizumab. Baseline levels of cir-EGFL7 were significantly related to PFS and OS, p = 0.0431 and p = 0.0017, respectively, with increasing cir-EGFL7 levels associated with a worse prognosis. Circulating EGFL7 was not associated with RR. The SNP analyses revealed a significant relationship between rs1051851 and OS, p = 0.030. This study demonstrates that cir-EGFL7 changes during treatment with chemotherapy plus bevacizumab and that baseline levels and genetic variations may influence the overall prognosis of patients with mCRC. The findings call for further validation.

摘要

高肿瘤表皮生长因子样结构域 7(EGFL7)的表达与结直肠癌的不良预后相关。本研究旨在探讨循环 EGFL7(cir-EGFL7)结合单核苷酸多态性(SNP)分析在接受一线化疗和贝伐单抗治疗的转移性结直肠癌(mCRC)患者中的可能预后影响。共纳入 88 例患者。在治疗开始前、第 3 周首次评估时和进展时采集血清。采用酶联免疫吸附试验(ELISA)技术分析 cir-EGFL7。采用实时 qPCR 分析基于全血 DNA 的 SNPs。终点是反应率(RR)、无进展生存期(PFS)和总生存期(OS)。化疗联合贝伐单抗治疗后 cir-EGFL7 降低。基线 cir-EGFL7 水平与 PFS 和 OS 显著相关,p=0.0431 和 p=0.0017,cir-EGFL7 水平升高与预后不良相关。循环 EGFL7 与 RR 无关。SNP 分析显示 rs1051851 与 OS 显著相关,p=0.030。本研究表明,化疗联合贝伐单抗治疗期间 cir-EGFL7 发生变化,基线水平和遗传变异可能影响 mCRC 患者的总体预后。研究结果需要进一步验证。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2b4e/5443778/55d8589ef5ab/41598_2017_2538_Fig1_HTML.jpg

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