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Overexpression of PVR and PD-L1 and its association with prognosis in surgically resected squamous cell lung carcinoma

Jii Bum Lee, Min Hee Hong, Sung Yong Park, Sehyun Chae, Daehee Hwang, Sang‐Jun Ha, Hyo Sup Shim, Hye Ryun Kim

2021Scientific Reports28 citationsDOIOpen Access PDF

Abstract

Targeting T-Cell Immunoreceptor with Ig and ITIM domain-poliovirus receptor (PVR) pathway is a potential therapeutic strategy in lung cancer. We analyzed the expression of PVR and programmed death ligand-1 (PD-L1) in surgically resected squamous cell lung carcinoma (SQCC) and determined its prognostic significance. We collected archival surgical specimens and data of 259 patients with SQCC at Yonsei Cancer Center (1998-2020). Analysis of variance was used to analyze the correlations between PVR and PD-L1 expression and patient characteristics. Kaplan-Meier curves were used to estimate recurrence-free survival (RFS) and overall survival (OS). Most patients were male (93%); the majority were diagnosed with stage 1 (47%), followed by stage 2 (29%) and stage 3 (21%). Overexpression of PVR resulted in a significantly shorter median RFS and OS (P = 0.01). PD-L1 expression was not significant in terms of prognosis. Patients were subdivided into four groups based on low and high PVR and PD-L1 expression. Those expressing high levels of PVR and PD-L1 had the shortest RFS (P = 0.03). PVR overexpression is associated with a poor prognosis in surgically resected SQCC. Inhibition of PVR as well as PD-L1 may help overcome the lack of response to immune checkpoint monotherapy.

Topics & Concepts

MedicineSquamous-cell carcinoma of the lungStage (stratigraphy)OncologyInternal medicinePD-L1Lung cancerCarcinomaImmunohistochemistryLungImmunotherapyCancerCancer researchBiologyPaleontologyCancer Immunotherapy and BiomarkersImmune Cell Function and InteractionImmunotherapy and Immune Responses