首页> 外文OA文献 >Prognostic value of programmed death-1, programmed death-ligand 1, programmed death-ligand 2 expression, and CD8(+) T cell density in primary tumors and metastatic lymph nodes from patients with stage T1-4N+M0 gastric adenocarcinoma
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Prognostic value of programmed death-1, programmed death-ligand 1, programmed death-ligand 2 expression, and CD8(+) T cell density in primary tumors and metastatic lymph nodes from patients with stage T1-4N+M0 gastric adenocarcinoma

机译:编程死亡-1,编程死亡配体1,编程的死亡配体2表达的预后价值,患有患者T1-4N + M0胃腺癌患者的原发性肿瘤和转移性淋巴结中的CD8(+)T细胞密度

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摘要

Abstract Background Anti-programmed death-1/programmed death-ligand 1 (PD-1/PD-L1) immunotherapy has been proved to be effective on gastric cancer in ongoing clinical trials. However, the value of PD-L1 in predicting responses of patients with gastric cancer to anti-PD-1/PD-L1 immunotherapy is controversial. Some studies suggested that intra- and inter-tumoral heterogeneity of PD-L1 expression might explain the controversy. This study aimed to analyze the expression of PD-L1, PD-L2, and PD-1 as well as CD8(+) T-cell density in primary tumors and lymph nodes from patients with stage T1-4N+M0 gastric adenocarcinoma to explore the heterogeneity of PD-1 signaling pathway molecules. Methods In primary tumors and metastatic as well as non-metastatic lymph nodes from patients with stage T1-4N+M0 gastric adenocarcinoma, we detected PD-L1 and PD-L2 expression with immunohistochemistry. CD8(+) T-cell density in primary tumors and PD-1 expression on CD8(+) T cells were detected with immunofluorescence. Univariate analysis was used to determine the prognostic values of them. Cox proportional hazard regression model was used to identify independent risk factors that affect patients’ overall survival and disease-free survival. Results Among 119 eligible patients who had undergone surgical resection, the positive rate of PD-L1 was higher in metastatic lymph nodes than in primary tumors (45.4% vs. 38.7%, P = 0.005); the positive rate of PD-1 on CD8(+) T cells was significantly higher in primary tumors and metastatic lymph nodes than in tumor-free lymph nodes (both P < 0.001). The intensity of PD-1 expression on CD8(+) T cells in primary tumors and in metastatic lymph nodes were stronger than that in tumor-free lymph nodes from the same patient. Beside, the positive rate of PD-L2 did not show any differences between primary tumors and metastatic lymph nodes. In multivariate analysis, PD-L1 expression, PD-L2 expression, a low density of CD8(+) T cells in primary tumors, and PD-1 expression on CD8(+) T cells in primary tumors were associated with poor prognosis. Conclusion The expression of PD-L1 is heterogeneous in primary tumors and in metastatic lymph nodes from patients with stage T1-4N+M0 gastric adenocarcinoma, which might explain the inconsistent results in assessing the prognostic value of PD-L1 expression in previous studies.
机译:摘要背景反编程死亡-1 /编程死亡 - 配体1(PD-1 / PD-L1)免疫疗法已被证明是对胃癌在持续的临床试验中有效。然而,PD-L1在预测抗PD-1 / PD-L1免疫疗法对胃癌患者的反应中的价值是有争议的。一些研究表明PD-L1表达的肿瘤间和肿瘤间异质性可能解释争议。本研究旨在分析PD-L1,PD-L2和PD-1,以及在原发肿瘤和淋巴结从患者阶段T1-4N + M0胃腺癌CD8(+)T细胞密度的表达探索PD-1信号传导分子的异质性。方法在原发性肿瘤和转移性以及非转移淋巴结从患者阶段T1-4N + M0胃腺癌,我们检测到免疫组化PD-L1和PD-L2的表达。 CD8(+)在原发性肿瘤的T细胞密度和PD-1的表达CD8(+)T细胞与免疫荧光进行检测。单变量分析用于确定它们的预后值。 COX比例危险回归模型用于识别影响患者整体生存和无病生存的独立风险因素。结果在119周符合条件的患者谁经历了手术切除,PD-L1的阳性率为转移性淋巴结比原发肿瘤(45.4%对38.7%,P = 0.005)更高; PD-1对CD8(+)T细胞的阳性率比在无肿瘤的淋巴结(均为P <0.001)在原发性肿瘤和转移淋巴结显著更高。 PD-1的表达对原发性肿瘤CD8(+)T细胞和淋巴结转移的强度均高于来自相同患者的无肿瘤的淋巴结更强。除此之外,PD-L2的阳性率没有显示原发性肿瘤和转移性淋巴结之间的任何差异。在多变量分析中,PD-L1表达,PD-L2表达,原发性肿瘤中的CD8(+)T细胞的低密度,以及原发性肿瘤中CD8(+)T细胞的PD-1表达与预后差有关。结论PD-L1的表达在原发性肿瘤中和阶段T1-4N + M0胃腺癌患者中的转移性淋巴结中的表达,这可能解释了评估先前研究中PD-L1表达的预后值的不一致结果。

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