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表皮生长因子受体和程序性死亡配体 1 共表达在食管鳞状细胞癌中的预后意义。

Prognostic significance of epidermal growth factor receptor and programmed cell death-ligand 1 co-expression in esophageal squamous cell carcinoma.

机构信息

Department of Oncology Radiotherapy, Yantaishan Hospital, Yantai 264025, Shandong, China.

Department of Oncology, Yantai Affiliated Hospital of Binzhou Medical University, Yantai 264000, Shandong, China.

出版信息

Aging (Albany NY). 2023 Feb 20;15(4):1107-1129. doi: 10.18632/aging.204535.

Abstract

Our study aimed to observe the correlation between epidermal growth factor receptor (EGFR) and programmed cell death-ligand 1 (PD-L1) expression and evaluate prognostic potential of their co-expression in esophageal squamous cell carcinoma (ESCC) patients. EGFR and PD-L1 expression were evaluated by immunohistochemical analysis. We revealed that there was a positive correlation between EGFR and PD-L1 expression in ESCC ( = 0.004). According to the positive relationship between EGFR and PD-L1, all patients were divided into four groups: EGFR (+)/PD-L1 (+), EGFR (+)/PD-L1 (-), EGFR (-)/PD-L1 (+), and EGFR (-)/PD-L1 (-). In 57 ESCC patients without surgery, we found that EGFR and PD-L1 co-expression were statistically correlated with a lower objective response rate (ORR) ( = 0.029), overall survival (OS) ( = 0.018) and progression-free survival (PFS) ( = 0.045) than those with one or none positive protein. Furthermore, PD-L1 expression has a significant positive correlation with infiltration level of 19 immune cells, EGFR expression was significantly correlated with infiltration level of 12 immune cells. The infiltration level of CD8 T cell and B cell were negatively correlated with EGFR expression. On the contrary with EGFR, the infiltration level of CD8 T cell, and B cell were positively correlated with PD-L1 expression. In conclusion, EGFR and PD-L1 co-expression could predict poor ORR and survival in ESCC without surgery, indicating a subset of patients who may benefit from a combination of targeted therapy against EGFR and PD-L1, which may expand the population benefiting from immunotherapy and reduce the occurrence of hyper progressive diseases.

摘要

我们的研究旨在观察表皮生长因子受体(EGFR)和程序性死亡配体 1(PD-L1)表达之间的相关性,并评估其在食管鳞状细胞癌(ESCC)患者中的共表达的预后潜力。通过免疫组织化学分析评估 EGFR 和 PD-L1 的表达。我们发现 EGFR 和 PD-L1 在 ESCC 中的表达呈正相关(=0.004)。根据 EGFR 和 PD-L1 之间的正相关关系,将所有患者分为四组:EGFR(+)/PD-L1(+)、EGFR(+)/PD-L1(-)、EGFR(-)/PD-L1(+)和 EGFR(-)/PD-L1(-)。在 57 例未接受手术的 ESCC 患者中,我们发现 EGFR 和 PD-L1 共表达与较低的客观缓解率(ORR)(=0.029)、总生存期(OS)(=0.018)和无进展生存期(PFS)(=0.045)呈统计学相关,而一个或没有阳性蛋白的患者则不是。此外,PD-L1 表达与 19 种免疫细胞浸润水平呈显著正相关,EGFR 表达与 12 种免疫细胞浸润水平呈显著正相关。CD8 T 细胞和 B 细胞的浸润水平与 EGFR 表达呈负相关。与 EGFR 相反,CD8 T 细胞和 B 细胞的浸润水平与 PD-L1 表达呈正相关。总之,在未经手术的 ESCC 患者中,EGFR 和 PD-L1 共表达可预测较差的 ORR 和生存,表明一部分患者可能受益于针对 EGFR 和 PD-L1 的靶向治疗联合治疗,这可能扩大受益于免疫治疗的人群,并减少超进展疾病的发生。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b5e6/10008495/b74c8c6a1470/aging-15-204535-g001.jpg

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