| 5-FU | 5-fluorouracil |
| AE | Adverse event |
| CI | Confidence interval |
| CPS | Combined positive score |
| CR | Complete response |
| CRP | C-reactive protein |
| CTCAE | National Cancer Institute Common Terminology Criteria for Adverse Events |
| DCR | Disease control rate |
| dMMR | Mismatch repair-deficient |
| DoR | Duration of response |
| ECOG | Eastern Cooperative Oncology Group |
| ESCC | Esophageal squamous cell carcinoma |
| FP | 5-fluorouracil and cisplatin |
| FFPE | Formalin-fixed paraffin-embedded |
| HR | Hazard ratio |
| ICI | Immune checkpoint inhibitor |
| IHC | Immunohistochemistry |
| irAE | Immune-related adverse event |
| IRB | Institutional review board |
| IV | Intravenously |
| MFDS | Ministry of Food and Drug Safety |
| MSI | Microsatellite instability |
| NGS | Next-generation sequencing |
| NLR | Neutrophil-to-lymphocyte ratio |
| ORR | Objective response rate |
| OS | Overall survival |
| PCR | Polymerase chain reaction |
| PD-1 | Programmed death-1 |
| PD-L1 | Programmed death-ligand 1 |
| PD | Progressive disease |
| PFS | Progression-free survival |
| PLR | Platelet-to-lymphocyte ratio |
| PR | Partial response |
| RECIST 1.1 | Response Evaluation Criteria in Solid Tumors version 1.1 |
| SCC | Squamous cell carcinoma |
| SD | Stable disease |
| TMB | Tumor mutation burden |
| TPS | Tumor proportion score |
| TRAE | Treatment-related adverse event |
| UNL | Upper normal limit |
| XP | Capecitabine and cisplatin |