Gene expression profile of high PD-L1 non-small cell lung cancers refractory to pembrolizumab.

Abstract

BACKGROUND:

Despite high expression of PD-L1, around half of advanced non-small cell lung cancer (NSCLC) will not experience tumor response with pembrolizumab. There is an need for a better understanding of the resistance mechanisms in this setting.

METHODS:

This bi-centric retrospective study included all consecutive patients with PDL1 ≥ 50% advanced NSCLC treated with pembrolizumab in first-line treatment between 2016 and 2020. We compared the clinical characteristics of patients with early progression (refractory) vs others. We performed a comprehensive gene expression profile screening by RNAseq capture on tumor samples.

RESULTS:

We included 46 patients. Twenty-two patients were refractory to pembrolizumab, mainly women, with poor performance status and lower albumin concentration. RNAseq analysis was performed on 19 samples. Hierarchical clustering allowed the identification of 3 clusters with various proportion of refractory tumors: intermediate (C1: 57%), high (C2: 71%) and low proportion (C3: 40%). Comparative analysis between C2 and C3 allowed the identification of overexpressed (n = 137) and underexpressed (n = 40) genes. Among the genes of interest, C2 exhibits higher activation of pathways associated with stemness phenotype (Hedgehog, Notch and Hippo pathways) and pathways associated with loss of PTEN and JAK2. In C2, genes associated with PD-1, toll-like receptor-9 (TLR-9), major histocompatibility complex (MHC) and interferon-γ pathways were underexpressed.

CONCLUSION:

This study gives an overview of activated and downregulated pathways in high PD-L1 NSCLC refractory to pembrolizumab. These tumors showed activation of pathways associated with cancer stem cells, loss of PTEN and JAK2, and inhibition of both priming and effector phases of the immune response.

• Authors: Jamila Talb, Paul Takam Kamga, Marie Mayenga, Adrien Costantini, Catherine Julié, Coraline Dumenil, Jennifer Dumoulin, Julia Ouaknine, Violaine Giraud, Cécile Dujon, Reza Azarian, Claire Glaser, Jean-François Emile, Etienne Giroux Leprieur
• Journal: Cancer immunology, immunotherapy : CII (Cancer Immunol Immunother) Vol. 71 Issue 11 Pg. 2791-2799 (Nov 2022) ISSN: 1432-0851 [Electronic] Germany
• PMID: 35435450 (Publication Type: Journal Article)
• Copyright: © 2022. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.

Chemical References

• Albumins
• Antibodies, Monoclonal, Humanized
• B7-H1 Antigen
• CD274 protein, human
• Programmed Cell Death 1 Receptor
• Toll-Like Receptor 9
• Interferon-gamma
• pembrolizumab

Topics

• Albumins (therapeutic use)
• Antibodies, Monoclonal, Humanized
• B7-H1 Antigen (metabolism)
• Carcinoma, Non-Small-Cell Lung (drug therapy, genetics, metabolism)
• Drug Resistance, Neoplasm
• Female
• Humans
• Interferon-gamma (therapeutic use)
• Lung Neoplasms (drug therapy, genetics, metabolism)
• Male
• Programmed Cell Death 1 Receptor
• Retrospective Studies
• Toll-Like Receptor 9 (metabolism)
• Transcriptome