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PD-L1 expression combined with microsatellite instability/CD8+ tumor infiltrating lymphocytes as a useful prognostic biomarker in gastric cancer

机译:PD-L1表达与微卫星不稳定性/ CD8 +肿瘤浸润淋巴细胞结合作为胃癌预后的有用生物标志物

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摘要

While the importance of programmed death-ligand 1 (PD-L1), mutation burden caused by microsatellite instability (MSI), and CD8+ tumor infiltrating lymphocytes (TILs) has become evident, the significance of PD-L1 expression on prognosis still remains controversial. We evaluated the usefulness of combined markers of PD-L1 and MSI or CD8+ TILs as a prognostic biomarker in gastric cancer. A total of 283 patients with gastric cancer were reviewed retrospectively. PD-L1 expression on >5% tumor cells was defined as PD-L1-positive. PD-L1-positive rate was 15.5% (44/283). PD-L1 positivity was significantly correlated with invasive and advanced cancer and also significantly correlated with MSI, whereas no significance was observed with CD8+ TILs. Kaplan–Meier analysis showed that PD-L1 positivity significantly correlated with a poor prognosis (p = 0.0025). Multivariate analysis revealed that PD-L1 positivity was an independent poor prognostic factor (hazard ratio [HR]: 1.97, p = 0.0106) along with diffuse histological type and lymph node metastases. Combinations of PD-L1 and MSI (HR: 2.18) or CD8+ TILs (HR: 2.57) were stronger predictive factors for prognosis than PD-L1 alone. In conclusion, combined markers of PD-L1 and MSI or CD8+ TILs may be more useful prognostic biomarkers in gastric cancer, and better clarify the immune status of gastric cancer patients.
机译:尽管程序性死亡配体1(PD-L1),由微卫星不稳定性(MSI)和CD8 +肿瘤浸润淋巴细胞(TILs)引起的突变负担的重要性已变得显而易见,但PD-L1表达对预后的重要性仍存在争议。我们评估了PD-L1和MSI或CD8 + TILs组合标志物作为胃癌预后生物标志物的有用性。回顾性分析了283例胃癌患者。 PD-L1在> 5%肿瘤细胞上的表达被定义为PD-L1阳性。 PD-L1阳性率为15.5%(44/283)。 PD-L1阳性与浸润性和晚期癌症显着相关,也与MSI显着相关,而CD8 + TILs则无显着性。 Kaplan–Meier分析显示PD-L1阳性与不良预后显着相关(p = 0.0025)。多变量分析显示PD-L1阳性是独立的不良预后因素(危险比[HR]:1.97,p = 0.0106)以及弥漫性组织学类型和淋巴结转移。与单独的PD-L1相比,PD-L1和MSI(HR:2.18)或CD8 + TILs(HR:2.57)的组合是更强的预后预测因素。总之,PD-L1和MSI或CD8 + TILs的组合标志物可能是更有用的胃癌预后生物标志物,并能更好地阐明胃癌患者的免疫状态。

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