CR |
complete response |
CT |
computer tomography |
CTLA-4 |
cytotoxic T-lymphocyte–associated protein 4 |
EGFR |
epidermal growth factor receptor |
EMA |
European Medicines Agency |
FDA |
Food and Drug Administration |
[18F]FDG |
2-deoxy-2-[18F]fluoro-D-glucose |
ICIs |
immune checkpoint inhibitors |
IHC |
immunohistochemistry |
irAE |
immune-related adverse event |
mAb |
monoclonal antibody |
MHC-I or -II |
major histocompatibility complex-I or -II |
MR |
magnetic resonance |
OS |
overall survival |
PD |
progressive disease |
PD-1 |
programmed cell death protein 1 |
PD-L1 |
programmed cell death ligand 1 |
PD-L2 |
programmed cell death ligand 2 |
PERCIMT |
PET Response Evaluation Criteria for Immunotherapy |
PERCIST |
positron emission tomography response criteria in solid tumors |
PET |
positron emission tomography |
PFS |
progression free survival |
PR |
partial response |
RECIST |
response evaluation criteria in solid tumors |
SD |
stable disease |
SUV |
standardized uptake value |
TCR |
T cell receptor |
TKI |
tyrosine kinase inhibitors |
TMB |
tumor mutational burden |
TME |
tumor microenvironment |
TPS |
tumor proportion score |