Purpose: Although targeting programmed death-1 (PD-1) and its ligand, programmed death-ligand 1 (PD-L1), is an established treatment modality for non-small cell lung cancer (NSCLC), the prognostic relevance of PD-L1 expression in NSCLC patients who undergo pulmonary resection is controversial.
Methods: Two hundred thirty-seven NSCLC patients who underwent pulmonary resection were enrolled and the relationship between PD-L1 and various clinicopathological factors, as well as the prognostic relevance of PD-L1, was evaluated.
Results: PD-L1 expression was significantly higher in male patients (p<0.01), lymphatic invasion (p<0.01), vascular invasion (p<0.01), grade 3–4 differentiation (p<0.01), squamous cell carcinoma (p<0.01), and pathological stage >II (p<0.01), but significantly lower in those who were epithelial growth factor receptor (EGFR) mutation-negative (p<0.01). Relapse-free survival was significantly worse in patients with PD-L1 expression (p=0.04). Univariate analysis showed that male sex (p=0.04), carcinoembryonic antigen expression (CEA) (p<0.01), maximum standardized uptake value (p<0.01), lymphatic invasion (p<0.01), vascular invasion (p<0.01), grade 3–4 differentiation (p<0.01), lower lobe disease (p=0.04), PD-L1 expression (p=0.03), and pathological stage (p<0.01) were significant risk factors of recurrence. In multivariate analysis, CEA expression (p=0.01), lymphatic invasion (p=0.04), and pathological stage (p<0.01) were risk factors for recurrence, whereas PD-L1 expression was not a significant factor of recurrence (p=0.62).
Conclusion: PD-L1 expression was not a risk factor of recurrence but tumor progression tended to increase PD-L1 expression.
Trial registration: The Institutional Review Board of Kanazawa Medical University approved the protocol of this retrospective study (approval number: I392), and written informed consent was obtained from all patients