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Clinical importance of VEGFC and PD‐L1 co‐expression in lung adenocarcinoma patients

机译:VEGFC和PD-L1在肺腺癌患者中共表达的临床重要性

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BACKGROUND:Vascular endothelial growth factor C (VEGFC), an activator of lymphangiogenesis, is newly identified as an immunomodulator which can regulate the immune system so that tumor cells more easily escape immune surveillance. Evidence has shown programmed cell death-ligand 1 (PD-L1) can also suppress the immune response. Nevertheless, the clinical significance of co-expression of VEGFC and PD-L1 for predicting outcomes in patients with lung adenocarcinoma has not yet been determined.METHODS:A total of 114 patients with lung adenocarcinoma who underwent surgeries at Tianjin Medical University Cancer Institute and Hospital between December 2011 and September 2016 were retrospectively reviewed. Tissue specimens were collected for immunohistochemistry of VEGFC and PD-L1 which were analyzed with an H-score system.RESULTS:In this study, 57 (50.0%) and 47 (41.2%) patients were classified as VEGFC high expression and PD-L1 high expression. Co-expression was observed in 33 (28.9%) patients. In addition, a positive correlation was found between VEGFC and PD-L1 (P = 0.0398, r = 0.1937). In a univariate analysis, both progression-free survival (PFS) and overall survival (OS) were significantly worse in the VEGFC high expression group and the PD-L1 high expression group, respectively. Furthermore, VEGFC/PD-L1 co-expression showed a worse OS (P = 0.03) and PFS survival (P = 0.01) than the other groups.CONCLUSIONS:Taken together, these results indicate that VEGFC/PD-L1 co-expression can forecast both poor OS and PFS in patients with resected lung adenocarcinoma. Co-expression of VEGFC and PD-L1 may serve as a significant prognostic factor for patients with lung adenocarcinoma.KEY POINTS:VEGFC/PD-L1 co-expression forecasts poor survival in patients with resected lung adenocarcinoma. VEGFC/PD-L1 co-expression may be used as a prognostic indicator and provide the theoretical possibility to screen the optimal population with a combination of anti-VEGFC and anti-PD-L1 therapy in the clinical treatment.? 2020 The Authors. Thoracic Cancer published by China Lung Oncology Group and John Wiley & Sons Australia, Ltd.
机译:背景:血管内皮生长因子C(VEGFC)是淋巴管发生的活化剂,是新鉴定为免疫调节器,可以调节免疫系统,使肿瘤细胞更容易逃避免疫监测。证据表明了细胞死亡 - 配体1(PD-L1)也可以抑制免疫应答。然而,VEGFC和PD-L1的临床意义尚未确定用于预测肺腺癌患者的结果。方法:共有114例肺腺癌患者,在天津医科大学癌症学院和医院接受手术2011年12月至2016年9月期间回顾性审查。收集组织标本用于VEGFC和PD-L1的免疫组化,用H-Score System进行分析。结果:在本研究中,57(50.0%)和47名(41.2%)患者被归类为VEGFC高表达和PD-L1高表达。在33名(28.9%)患者中观察到共表达。此外,在VEGFC和PD-L1之间发现阳性相关(P = 0.0398,R = 0.1937)。在单变量分析中,VEGFC高表达组和PD-L1高表达基团的无进展生存期(PFS)和总存活(OS)显着差。此外,VEGFC / PD-L1共表达显示出比其他组更差的OS(P = 0.03)和PFS存活率(P = 0.01)。结论:组合在一起,这些结果表明VEGFC / PD-L1共表达可以预测切除肺腺癌患者患者的贫困型号和PFS。 VEGFC和PD-L1的共同表达可以作为肺腺癌患者的显着预后因素。(PRECE):VEGFC / PD-L1共同表达预测肺癌患者的患者存活率差。 VEGFC / PD-L1共表达可以用作预后指示剂,并提供在临床治疗中用抗VEGFC和抗PD-L1治疗的组合筛选最佳群体的理论可能性。? 2020作者。中国肺部肿瘤集团和约翰瓦里和儿子澳大利亚发表的胸癌

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