Prognostic and predictive role of CD8 and PD-L1 determination in lung tumor tissue of patients under anti-PD-1 therapy

Jean-David Fumet(Université de Bourgogne), Corentin Richard(Université de Bourgogne), Fanny Ledys(Université de Bourgogne), Quentin Klopfenstein(Genomic and Immunotherapy Medical Institute), Philippe Joubert(Institut universitaire de cardiologie et de pneumologie de Québec), Bertrand Routy(Centre Hospitalier de l’Université de Montréal), Caroline Truntzer(Genomic and Immunotherapy Medical Institute), Andréanne Gagné(Institut universitaire de cardiologie et de pneumologie de Québec), Marc-André Hamel(Institut universitaire de cardiologie et de pneumologie de Québec), Camila Figueiredo Guimaraes(Institut universitaire de cardiologie et de pneumologie de Québec), Bruno Coudert(Centre Georges François Leclerc), Laurent Arnould(Centre Georges François Leclerc), Laure Favier(Centre Georges François Leclerc), Aurélie Lagrange(Centre Georges François Leclerc), Sylvain Ladoire(Université de Bourgogne), Pierre Saintigny(Centre Léon Bérard), Sandra Ortiz‐Cuaran(Centre Léon Bérard), M. Pérol(Centre Léon Bérard), Pascal Foucher(CHU Dijon Bourgogne), Paul Hofman(Université Côte d'Azur), Marius Ilié(Université Côte d'Azur), Sandy Chevrier(Genomic and Immunotherapy Medical Institute), Romain Boidot(Genomic and Immunotherapy Medical Institute), Valentin Dérangère(Genomic and Immunotherapy Medical Institute), François Ghiringhelli(Inserm)
British Journal of Cancer
October 1, 2018
Cited by 173Open Access
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Abstract

BACKGROUND: No study has evaluated the predictive and prognostic role of CD8 and PD-L1 coexpression in non-small-cell lung cancer (NSCLC). METHODS: We analyzed RNA sequencing and/or immunohistochemistry staining in NSCLC patients from The Cancer Genome Atlas (n = 1016), and 34 metastatic NSCLC samples not treated by immunotherapy as prognostic cohorts. As predictive aspect of CD8 and PD-L1, we used 85 NSCLC patients treated with anti-PD-1. Two validation cohorts were used including 44 NSCLC patients treated with anti-PD-1 and an external cohort with different tumor types. RESULTS: In prognostic cohorts, high CD8A expression was associated with longer OS (p = 0.02), while high CD274 mRNA was associated with poor prognosis (p = 0.05). In predictive cohort, high CD8 expression and CD8A mRNA were associated with longer progression-free survival (PFS) (p = 0.0002). There was no significant association between PD-L1 expression and PFS while high CD274 mRNA was associated with longer PFS (p = 0.009). A combination of CD8A and CD274 was highly predictive of outcome. These results were confirmed in the validation cohorts. This two-genes signature demonstrated similar results compared to gold standard signatures. CONCLUSION: CD8 represents both a prognostic and predictive factor of outcomes, while PD-L1 share different prognostic and predictive roles.


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