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Prognostic value and clinicopathological features of PD-1/PD-L1 expression with mismatch repair status and desmoplastic stroma in Chinese patients with pancreatic cancer

机译:PD-1 / PD-L1表达与错配修复状态和增生基质在中国胰腺癌患者中的预后价值和临床病理特征

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摘要

Pancreatic cancer (PC) is a highly lethal cancer. Thus, the immune molecular markers which help to select PC patients are especially important. In this study, we aimed at systematically analyzing the expression of MLH1, MSH2, PD-L1 and PD-1, investigate their clinical significance and prognostic value. We found that high expression of PD-L1 on cancer cell membranes correlated with lymph node metastasis (P = 0.033) and strongly correlated with poor-differentiation (P = 0.008); high expression of PD-1 on cell membranes of T-cells correlated with well-differentiation (P = 0.018) and strongly correlated with advanced T stage (P = 0.004); high PD-1 expression was associated with a significantly superior OS and was an independent prognostic factor (P = 0.031). Then we found an inverse correlation between MSH2 expression and PD-L1 expression (Spearman correlation coefficient r = −0.295, P = 0.004). In subgroup analyses, we observed that PD-1 expression level was associated with OS only at low PD-L1 expression subgroup (P = 0.021). Finally, when we stratified the cases into four subgroups based on PD-1 expression and stroma density, we found that patients with high PD-1 expression and dense stroma had a better OS, while patients with low PD-1 expression and moderate stroma showed a worst outcome. Our result may provide more effective molecular markers for immunotherapeutic strategies of PC patients in clinical practice.
机译:胰腺癌(PC)是一种高度致死性的癌症。因此,有助于选择PC患者的免疫分子标记尤为重要。本研究旨在系统地分析MLH1,MSH2,PD-L1和PD-1的表达,探讨其临床意义和预后价值。我们发现PD-L1在癌细胞膜上的高表达与淋巴结转移有关(P = 0.033),与分化差有关(P = 0.008)。 PD-1在T细胞细胞膜上的高表达与分化良好相关(P = 0.018),与晚期T期高度相关(P = 0.004);高PD-1表达与明显更好的OS相关,并且是独立的预后因素(P = 0.031)。然后,我们发现MSH2表达与PD-L1表达之间呈负相关(Spearman相关系数r = -0.295,P = 0.004)。在亚组分析中,我们观察到PD-1表达水平仅在低PD-L1表达亚组与OS相关(P = 0.021)。最后,当我们根据PD-1表达和基质密度将病例分为四个亚组时,我们发现高PD-1表达和密集基质的患者的OS更好,而低PD-1表达和中等基质的患者显示最糟糕的结果。我们的结果可能为临床实践中PC患者的免疫治疗策略提供更有效的分子标记。

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