Research Paper Volume 15, Issue 4 pp 1107—1129

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

Guoxiang Jiang1, , Yandong Miao2, , Zhenbo Wang3, , Qi Zhang4, , Ping Zhou4, , Fang Zhang5, ,

  • 1 Department of Oncology Radiotherapy, Yantaishan Hospital, Yantai 264025, Shandong, China
  • 2 Department of Oncology, Yantai Affiliated Hospital of Binzhou Medical University, Yantai 264000, Shandong, China
  • 3 Department of Radiation Oncology, Binzhou Affiliated Hospital of Binzhou Medical University, Binzhou 256603, Shandong, China
  • 4 Department of Pathology, The First Hospital of Zibo, Zibo 255200, Shandong, China
  • 5 Department of Radiation Oncology, Yantai Affiliated Hospital of Binzhou Medical University, Yantai 26400, Shandong, China

Received: October 14, 2022       Accepted: February 6, 2023       Published: February 20, 2023      

https://doi.org/10.18632/aging.204535
How to Cite

Copyright: © 2023 Jiang et al. This is an open access article distributed under the terms of the Creative Commons Attribution License (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

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 (P = 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) (p = 0.029), overall survival (OS) (p = 0.018) and progression-free survival (PFS) (p = 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.

Abbreviations

EC: esophageal cancer; EGF: epidermal growth factor; EGFR: epidermal growth factor receptor; ESCC: esophageal squamous cell carcinoma; IHC: immunohistochemical; ORR: objective response rate; OS: overall survival; PD-1: programmed cell death-1; PD-L1: programmed cell death ligand 1; PFS: progression-free survival; TME: immunosuppressive tumor microenvironment.