更正:B7-H3 CAR T 细胞清除肝内胆管癌并诱导持久应答
Correction: B7-H3 CAR T cells eradicate intrahepatic cholangiocarcinoma and induce durable response.
英文原题:Prognostic value of Dickkopf-1 and ß-catenin expression according to the antitumor immunity of CD8-positive tumor-infiltrating lymphocytes in biliary tract cancer.
我们使用了癌症基因组图谱研究网络的数据以及2006年至2016年间接受原发性根治性切除术的145例BTC患者的临床病理数据。
β-catenin和Dickkopf-1(DKK1)的作用取决于胆道癌(BTC)中T细胞炎症的特定免疫生物学。我们旨在分析DKK1或β-catenin作为BTC预后因素的作用,并确定β-catenin和DKK1与CD8+TIL(肿瘤浸润淋巴细胞)的临床关联。我们使用了癌症基因组图谱研究网络的数据以及2006年至2016年间接受原发性根治性切除术的145例BTC患者的临床病理数据。CD8+ TIL表达是有利的总生存期(OS)和无复发生存期(RFS)的显著预测因子(中位OS,高TIL组34.9个月,低TIL组16.7个月,P < 0.0001;中位RFS,高TIL组27.1个月,低TIL组10.0个月,P < 0.0001)。在高CD8+ TIL的BTC组中,肿瘤表达β-catenin和DKK1对OS或RFS均有显著的负面影响。在低TIL的BTC组中,β-catenin和DKK1表达之间没有差异。Cox回归多变量分析表明,CD8+ TIL和β-catenin与OS保持显著关联。在切除的BTC患者中,β-catenin和DKK1蛋白以及高CD8+ TIL水平分别与不良和良好的临床结局相关。
The role of -catenin and Dickkopf-1 (DKK1) is dependent on the specific immunobiology of T cell inflammation in biliary tract cancer (BTC). We aimed to analyze the role of DKK1 or -catenin as a prognostic factor in BTC, and determine the clinical associations of -catenin and DKK1 with CD8+ tumor-infiltrating lymphocytes (TIL). We used data from The Cancer Genome Atlas Research Network and the clinicopathological data of 145 patients with BTC who had undergone primary radical resection between 2006 and 2016. CD8+ TIL expression was a significant predictor of favorable overall survival (OS) and relapse-free survival (RFS) (median OS, 34.9 months in high-TIL, 16.7 months in low-TIL, P < 0.0001 respectively; median RFS, 27.1 months in high-TIL, 10.0 months in low-TIL, P < 0.0001 respectively). In the high-CD8+ TIL BTC group, the tumor expression of -catenin and DKK1 had a significant negative impact on either OS or RFS. In the low-TIL BTC group, there were no differences according to -catenin and DKK1 expression. Cox regression multivariate analysis demonstrated that CD8+ TIL and -catenin retained significant association with OS. Among patients with resected BTC, the -catenin and DKK1 protein and high CD8+ TIL levels were associated with poor and good clinical outcomes, respectively.
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