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VEGF和VEGFR基因多态性对接受舒尼替尼治疗的转移性肾细胞癌患者预后的影响:一项系统评价和荟萃分析

Effects of VEGF and VEGFR polymorphisms on the outcome of patients with metastatic renal cell carcinoma treated with sunitinib: a systematic review and meta-analysis.

作者信息

Miao Chenkui, Cao Jingyi, Wang Yuhao, Liu Bianjiang, Wang Zengjun

机构信息

State Key Laboratory of Reproductive Medicine and Department of Urology, The First Affiliated Hospital of Nanjing Medical University, Nanjing, China.

Department of Urology, Xuzhou Cancer Hospital, Xuzhou, China.

出版信息

Oncotarget. 2017 Aug 4;8(40):68854-68862. doi: 10.18632/oncotarget.19924. eCollection 2017 Sep 15.

Abstract

To summarize and clarify the association between vascular endothelial growth factor () and vascular endothelial growth factor receptor () polymorphisms and the outcome in patients with metastatic renal cell carcinoma (mRCC) treated with sunitinib. A total of 8 studies including 900 patients were analyzed in this systematic review after screening the database of PubMed, EMBASE and Web of Science. Hazard ratios (HRs) with 95% confidence interval (CI) were used to evaluate the strength of the association. VEGFR1 rs9582036 AA/AC carriers and rs9554320 CC/AC carriers had more favorable overall survival (OS) in patients with mRCC treated with sunitinib ( = 3), but not in progression-free survival (PFS). In addition, rs2010963 was associated with poorer PFS of mRCC ( = 1). rs699947 was significant in predicting PFS by univariate analysis, but showed no statistical significance in OS ( = 1). rs1870377 was verified to be associated with sunitinib OS ( = 1). Furthermore, patients with rs307826 and rs307821 had shorter PFS and OS during sunitinib therapy ( = 2, respectively). Our results suggested that and polymorphisms were associated with outcomes in sunitinib treated mRCC patients, especially polymorphisms. However, considering the limited study numbers, its clinical application in sunitinib treated mRCC still needs further confirmation.

摘要

总结并阐明血管内皮生长因子(VEGF)和血管内皮生长因子受体(VEGFR)基因多态性与接受舒尼替尼治疗的转移性肾细胞癌(mRCC)患者预后之间的关联。在筛选PubMed、EMBASE和Web of Science数据库后,本系统评价共分析了8项研究,包括900例患者。采用95%置信区间(CI)的风险比(HRs)来评估关联强度。VEGFR1 rs9582036 AA/AC携带者和rs9554320 CC/AC携带者在接受舒尼替尼治疗的mRCC患者中总生存期(OS)更优(n = 3),但无进展生存期(PFS)并非如此。此外,VEGFR2 rs2010963与mRCC的PFS较差相关(n = 1)。VEGFR3 rs699947在单因素分析中对PFS有显著预测作用,但在OS中无统计学意义(n = 1)。VEGFR3 rs1870377被证实与舒尼替尼OS相关(n = 1)。此外,携带VEGFR1 rs307826和rs307821的患者在舒尼替尼治疗期间PFS和OS较短(分别为n = 2)。我们的结果表明,VEGF和VEGFR基因多态性与舒尼替尼治疗的mRCC患者的预后相关,尤其是VEGFR基因多态性。然而,考虑到研究数量有限,其在舒尼替尼治疗的mRCC中的临床应用仍需进一步证实。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/71fe/5620302/aa3321b3b77a/oncotarget-08-68854-g001.jpg

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