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ABSTRACT: Introduction
Immune checkpoint inhibition has shifted treatment paradigms in non-small cell lung cancer (NSCLC). Conflicting results have been reported regarding the immune infiltrate and programmed death-ligand 1 (PD-L1) as a prognostic marker. We correlated the immune infiltrate and PD-L1 expression with clinicopathologic characteristics in a cohort of resected NSCLC.Methods
A tissue microarray was constructed using triplicate cores from consecutive resected NSCLC. Immunohistochemistry was performed for CD8, FOXP3 and PD-L1. Strong PD-L1 expression was predefined as greater than 50% tumor cell positivity. Matched nodal samples were assessed for concordance of PD-L1 expression.Results
Of 522 patients, 346 were node-negative (N0), 72 N1 and 109 N2; 265 were adenocar
SUBMITTER: Ameratunga M
PROVIDER: S-EPMC4841565 | biostudies-literature | 2016
REPOSITORIES: biostudies-literature