PD-L1 Expression and Tumour Microenvironment Patterns in Resected Non-Small-Cell Lung Cancer.
Giedrė GurevičienėJurgita MatulionėLina PoškienėSkaidrius MiliauskasMarius ŽemaitisPublished in: Medicina (Kaunas, Lithuania) (2024)
Background and Objectives : Although perioperative immunotherapy is implemented as a standard of care for resected non-small cell lung cancer (NSCLC), there is unmet need for predictive biomarkers as programmed death-ligand 1 (PD-L1) is not the perfect one. The functionality of tumour-infiltrating immune cells in the tumour microenvironment (TME) and the involvement in immune system response is one of the crucial factors that lead to pro- or anti-tumourigenic role and could predict response to PD-1 and PD-L1 inhibitors. So, the investigation of PD-L1 expression in the context of TME in early stages of resected NSCLC is urgent required. Materials and Methods : PD-L1 expression by three scoring methods: tumour proportion score (TPS), immune cell score (IC), and combined proportion score (CPS) was assessed in 72 archival tumour tissue specimens from stage I-III surgically resected NSCLC patients and associations with immune cells in TME were explored. Results : PD-L1 expression ≥1% evaluated by TPS, IC, and CPS was detected in 28%, 36%, and 39% of cases and moderate, substantial, and strong agreement between TPS and IC, TPS and CPS, CPS and IC was detected (Cohen's κ coefficient 0.556, 0.63, and 0.941, respectively). PD-L1 TPS, IC, and CPS correlated with smoking intensity defined as pack-years (r = 0.0305, p = 0.012; r = 0.305, p = 0.013, and r = 0.378, p = 0.002, respectively). Only PD-L1 TPS was associated with squamous cell carcinoma ( p = 0.028). PD-L1 IC ≥1% was more often seen in tumours with high CD4 + T cells infiltration ( p = 0.02), while PD-L1 CPS ≥1%-in tumours with high CD4 + and CD8 + T cells infiltration ( p = 0.021 and p = 0.048, respectively). PD-L1 IC and CPS ≥10% was more often detected in tumours with greater number of tumour-infiltrating CD4 + Foxp3 + T cells ( p = 0.01 and p = 0.025, respectively). PD-L1 TPS ≥50% was associated with higher probability to detect greater number of tumour-infiltrating M2 macrophages ( p = 0.021). No association was found between PD-L1 alone or in combination with tumour-infiltrating lymphocytes, macrophages, and disease-free or overall survival. Conclusions : This study results revealed that rates of PD-L1 expression correlated among three scoring methods (TPS, IC, and CPS). Moreover, PD-L1 expression was significantly associated with smoking intensity, squamous histology, and tumour-infiltrating immune cells.
Keyphrases
- squamous cell carcinoma
- small cell lung cancer
- lymph node
- prognostic factors
- stem cells
- healthcare
- high intensity
- palliative care
- computed tomography
- ejection fraction
- end stage renal disease
- smoking cessation
- advanced non small cell lung cancer
- regulatory t cells
- newly diagnosed
- radiation therapy
- magnetic resonance imaging
- single cell
- quality improvement
- locally advanced
- high grade
- chronic pain
- tyrosine kinase
- dendritic cells
- nk cells
- free survival
- patient reported