...
首页> 外文期刊>Annals of surgical oncology >Soluble PD-L1 Expression in Circulation as a Predictive Marker for Recurrence and Prognosis in Gastric Cancer: Direct Comparison of the Clinical Burden Between Tissue and Serum PD-L1 Expression
【24h】

Soluble PD-L1 Expression in Circulation as a Predictive Marker for Recurrence and Prognosis in Gastric Cancer: Direct Comparison of the Clinical Burden Between Tissue and Serum PD-L1 Expression

机译:循环中可溶的PD-L1表达作为胃癌复发和预后的预测标志物:直接比较组织与血清PD-L1表达的临床负担

获取原文
获取原文并翻译 | 示例

摘要

BackgroundThis study assessed programmed cell death ligand 1 (PD-L1) expression in primary tissues and soluble PD-L1 (sPD-L1) concentration in matched preoperative serum in gastric cancer (GC) patients to perform direct comparison between tissue and serum PD-L1 expression and to clarify the prognostic implication in GC.MethodsThe study enrolled 180 GC patients who underwent surgery for GC at the authors' institution. The study evaluated tissue PD-L1 expression using immunohistochemistry and quantified sPD-L1 concentration in preoperative serum using enzyme-linked immunosorbent assay in GC patients.ResultsThe findings showed that PD-L1 was overexpressed in GC tissues compared with normal mucosa. Tissue PD-L1 expression was significantly higher in the GC patients with advanced T stage, presence of lympho-vascular invasion, lymph node metastasis, and peritoneal metastasis. Furthermore, elevated tissue PD-L1 expression was significantly associated with poor prognosis for overall survival (OS) and disease-free survival (DFS). Serum sPD-L1 was significantly higher in the GC patients than in the healthy volunteers. Although serum sPD-L1 was not correlated with any clinicopathologic factors, the patients with high serum sPD-L1 showed poorer OS and DFS than those with low sPD-L1. Multivariate analyses showed that both elevated tissue PD-L1 and serum sPD-L1 were independent prognostic factors for poor OS [tissue PD-L1: hazard ratio (HR), 4.28; 95% confidence interval (CI), 1.43-12.8; P=0.0094 vs. serum sPD-L1: HR, 11.2; 95% CI, 3.44-36.7; P=0.0001] and poor DFS (tissue PD-L1: HR, 6.96; 95% CI, 2.48-19.6; P=0.0002 vs. serum sPD-L1: HR, 8.7; 95% CI, 3.16-23.9; P0.0001) for the GC patients. Furthermore, infiltrative CD8- and Foxp3-positive T cells were significantly increased in the GC patients with elevated tissue PD-L1 expression.ConclusionBoth serum sPD-L1 and tissue PD-L1 expression may serve as predictive biomarkers for recurrence and prognosis in GC patients.
机译:背景技术评估胃癌(GC)患者匹配的术前血清中的主要组织和可溶性PD-L1(SPD-L1)浓度的编程细胞死亡配体1(PD-L1)表达,以在组织和血清PD-L1之间进行直接比较表达并阐明了GC.Methodsthe研究的预后意蕴注册了180名GC患者在作者机构的GC接受外科手术。该研究评估了在GC患者中使用酶联免疫吸附测定的术前血清中的免疫组织化学和定量的SPD-L1浓度评估了组织PD-L1表达。结果表明,与正常粘膜相比,PD-L1在GC组织中过表达。 GC患者在高级T阶段,淋巴血管侵袭,淋巴结转移和腹膜转移的存在显着较高。此外,升高的组织PD-L1表达与总存活率(OS)和无病生存率(DFS)的预后差显着相关。 GC患者的血清SPD-L1显着高于健康的志愿者。尽管血清SPD-L1与任何临床病理因素没有相关,但高血清SPD-L1的患者显示较差的OS和DF,而不是具有低SPD-L1的OS和DF。多变量分析表明,升高的组织PD-L1和血清SPD-L1是差的OS [组织PD-L1:危害比(HR),4.28; 95%置信区间(CI),1.43-12.8; P = 0.0094与血清SPD-L1:HR,11.2; 95%CI,3.44-36.7; P = 0.0001]和DFS差(组织PD-L1:HR,6.96; 95%CI,2.48-19.6; P = 0.0002与血清SPD-L1:HR,8.7; 95%CI,3.16-23.9; P <0.0001 )对于GC患者。此外,在组织PD-L1表达升高的GC患者中,渗透CD8-和FoxP3阳性T细胞显着增加。结论血清SPD-L1和组织PD-L1表达可作为GC患者复发和预后的预测生物标志物。

著录项

  • 来源
    《Annals of surgical oncology 》 |2019年第3期| 共8页
  • 作者单位

    Mie Univ Dept Gastrointestinal &

    Pediat Surg Grad Sch Med Div Reparat Med Inst Life Sci Tsu;

    Mie Univ Dept Gastrointestinal &

    Pediat Surg Grad Sch Med Div Reparat Med Inst Life Sci Tsu;

    Mie Univ Dept Gastrointestinal &

    Pediat Surg Grad Sch Med Div Reparat Med Inst Life Sci Tsu;

    Mie Univ Dept Gastrointestinal &

    Pediat Surg Grad Sch Med Div Reparat Med Inst Life Sci Tsu;

    Mie Univ Dept Gastrointestinal &

    Pediat Surg Grad Sch Med Div Reparat Med Inst Life Sci Tsu;

    Mie Univ Dept Gastrointestinal &

    Pediat Surg Grad Sch Med Div Reparat Med Inst Life Sci Tsu;

    Mie Univ Dept Gastrointestinal &

    Pediat Surg Grad Sch Med Div Reparat Med Inst Life Sci Tsu;

    Mie Univ Dept Gastrointestinal &

    Pediat Surg Grad Sch Med Div Reparat Med Inst Life Sci Tsu;

    Mie Univ Dept Gastrointestinal &

    Pediat Surg Grad Sch Med Div Reparat Med Inst Life Sci Tsu;

    Mie Univ Dept Gastrointestinal &

    Pediat Surg Grad Sch Med Div Reparat Med Inst Life Sci Tsu;

    Mie Univ Dept Gastrointestinal &

    Pediat Surg Grad Sch Med Div Reparat Med Inst Life Sci Tsu;

    Mie Univ Dept Gastrointestinal &

    Pediat Surg Grad Sch Med Div Reparat Med Inst Life Sci Tsu;

    Mie Univ Dept Gastrointestinal &

    Pediat Surg Grad Sch Med Div Reparat Med Inst Life Sci Tsu;

    Mie Univ Dept Gastrointestinal &

    Pediat Surg Grad Sch Med Div Reparat Med Inst Life Sci Tsu;

    Mie Univ Dept Gastrointestinal &

    Pediat Surg Grad Sch Med Div Reparat Med Inst Life Sci Tsu;

    Mie Univ Dept Gastrointestinal &

    Pediat Surg Grad Sch Med Div Reparat Med Inst Life Sci Tsu;

  • 收录信息
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 外科学 ;
  • 关键词

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号