Programmed death‐ligand 1 gene expression is a prognostic marker in early breast cancer and provides additional prognostic value to 21‐gene and 70‐gene signatures in estrogen receptor‐positive disease

Gene and protein expression of programmed death‐ligand 1 (PD‐L1) are prognostic in early breast cancer (BC), but their prognostic information is inconsistent at least in some biological subgroups. The validated prognostic gene signatures (GS) in BC are mainly based on proliferation and estrogen rece...

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Main Authors: Ioannis Zerdes, Emmanouil G. Sifakis, Alexios Matikas, Sebastian Chrétien, Nicholas P. Tobin, Johan Hartman, George Z. Rassidakis, Jonas Bergh, Theodoros Foukakis
Format: Article
Language:English
Published: Wiley 2020-05-01
Series:Molecular Oncology
Subjects:
Online Access:https://doi.org/10.1002/1878-0261.12654
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author Ioannis Zerdes
Emmanouil G. Sifakis
Alexios Matikas
Sebastian Chrétien
Nicholas P. Tobin
Johan Hartman
George Z. Rassidakis
Jonas Bergh
Theodoros Foukakis
author_facet Ioannis Zerdes
Emmanouil G. Sifakis
Alexios Matikas
Sebastian Chrétien
Nicholas P. Tobin
Johan Hartman
George Z. Rassidakis
Jonas Bergh
Theodoros Foukakis
author_sort Ioannis Zerdes
collection DOAJ
description Gene and protein expression of programmed death‐ligand 1 (PD‐L1) are prognostic in early breast cancer (BC), but their prognostic information is inconsistent at least in some biological subgroups. The validated prognostic gene signatures (GS) in BC are mainly based on proliferation and estrogen receptor (ER)‐related genes. Here, we aimed to explore the prognostic capacity of PD‐L1 expression at the protein vs mRNA levels and to investigate the prognostic information that PD‐L1 can potentially add to routinely used GS. Gene expression data were derived from two early BC cohorts (cohort 1: 562 patients; cohort 2: 1081 patients). Tissue microarrays from cohort 1 were immunohistochemically (IHC) stained for PD‐L1 using the SP263 clone. GS scores (21‐gene, 70‐gene) were calculated, and likelihood‐ratio (LR) tests and concordance indices were used to evaluate the additional prognostic information for each signature. The immune cell composition was also evaluated using the CIBERSORT in silico tool. PD‐L1 gene and protein expressions were independently associated with better prognosis. In ER+/HER2− patients, PD‐L1 gene expression provided significant additional prognostic information beyond that of both 21‐GS [LR‐Δχ2 = 15.289 and LR‐Δχ2 = 8.812, P < 0.01 for distant metastasis‐free interval (DMFI) in cohorts 1 and 2, respectively] and 70‐GS score alone (LR‐Δχ2 = 18.198 and LR‐Δχ2 = 8.467, P < 0.01 for DMFI in cohorts 1 and 2, respectively). PD‐L1 expression was correlated with IHC‐determined CD3+ cells (r = 0.41, P < 0.001) and with CD8+ (r = 0.62, P < 0.001) and CD4+ memory activated (r = 0.66, P < 0.001) but not with memory resting (r = −0.063, P = 0.14) or regulatory (r = −0.12, P < 0.01) T cells in silico. PD‐L1 gene expression represents a promising favorable prognostic marker and can provide additional prognostic value to 21‐ and 70‐gene scores in ER+/HER2− BC.
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spelling doaj.art-35cba073e6ea4fa1bf36cbaeb5a2366b2022-12-21T23:52:17ZengWileyMolecular Oncology1574-78911878-02612020-05-0114595196310.1002/1878-0261.12654Programmed death‐ligand 1 gene expression is a prognostic marker in early breast cancer and provides additional prognostic value to 21‐gene and 70‐gene signatures in estrogen receptor‐positive diseaseIoannis Zerdes0Emmanouil G. Sifakis1Alexios Matikas2Sebastian Chrétien3Nicholas P. Tobin4Johan Hartman5George Z. Rassidakis6Jonas Bergh7Theodoros Foukakis8Department of Oncology‐Pathology Karolinska Institute Stockholm SwedenDepartment of Oncology‐Pathology Karolinska Institute Stockholm SwedenDepartment of Oncology‐Pathology Karolinska Institute Stockholm SwedenDepartment of Oncology‐Pathology Karolinska Institute Stockholm SwedenDepartment of Oncology‐Pathology Karolinska Institute Stockholm SwedenDepartment of Oncology‐Pathology Karolinska Institute Stockholm SwedenDepartment of Oncology‐Pathology Karolinska Institute Stockholm SwedenDepartment of Oncology‐Pathology Karolinska Institute Stockholm SwedenDepartment of Oncology‐Pathology Karolinska Institute Stockholm SwedenGene and protein expression of programmed death‐ligand 1 (PD‐L1) are prognostic in early breast cancer (BC), but their prognostic information is inconsistent at least in some biological subgroups. The validated prognostic gene signatures (GS) in BC are mainly based on proliferation and estrogen receptor (ER)‐related genes. Here, we aimed to explore the prognostic capacity of PD‐L1 expression at the protein vs mRNA levels and to investigate the prognostic information that PD‐L1 can potentially add to routinely used GS. Gene expression data were derived from two early BC cohorts (cohort 1: 562 patients; cohort 2: 1081 patients). Tissue microarrays from cohort 1 were immunohistochemically (IHC) stained for PD‐L1 using the SP263 clone. GS scores (21‐gene, 70‐gene) were calculated, and likelihood‐ratio (LR) tests and concordance indices were used to evaluate the additional prognostic information for each signature. The immune cell composition was also evaluated using the CIBERSORT in silico tool. PD‐L1 gene and protein expressions were independently associated with better prognosis. In ER+/HER2− patients, PD‐L1 gene expression provided significant additional prognostic information beyond that of both 21‐GS [LR‐Δχ2 = 15.289 and LR‐Δχ2 = 8.812, P < 0.01 for distant metastasis‐free interval (DMFI) in cohorts 1 and 2, respectively] and 70‐GS score alone (LR‐Δχ2 = 18.198 and LR‐Δχ2 = 8.467, P < 0.01 for DMFI in cohorts 1 and 2, respectively). PD‐L1 expression was correlated with IHC‐determined CD3+ cells (r = 0.41, P < 0.001) and with CD8+ (r = 0.62, P < 0.001) and CD4+ memory activated (r = 0.66, P < 0.001) but not with memory resting (r = −0.063, P = 0.14) or regulatory (r = −0.12, P < 0.01) T cells in silico. PD‐L1 gene expression represents a promising favorable prognostic marker and can provide additional prognostic value to 21‐ and 70‐gene scores in ER+/HER2− BC.https://doi.org/10.1002/1878-0261.12654breast cancergene expressiongene signaturesPD‐L1prognosis
spellingShingle Ioannis Zerdes
Emmanouil G. Sifakis
Alexios Matikas
Sebastian Chrétien
Nicholas P. Tobin
Johan Hartman
George Z. Rassidakis
Jonas Bergh
Theodoros Foukakis
Programmed death‐ligand 1 gene expression is a prognostic marker in early breast cancer and provides additional prognostic value to 21‐gene and 70‐gene signatures in estrogen receptor‐positive disease
Molecular Oncology
breast cancer
gene expression
gene signatures
PD‐L1
prognosis
title Programmed death‐ligand 1 gene expression is a prognostic marker in early breast cancer and provides additional prognostic value to 21‐gene and 70‐gene signatures in estrogen receptor‐positive disease
title_full Programmed death‐ligand 1 gene expression is a prognostic marker in early breast cancer and provides additional prognostic value to 21‐gene and 70‐gene signatures in estrogen receptor‐positive disease
title_fullStr Programmed death‐ligand 1 gene expression is a prognostic marker in early breast cancer and provides additional prognostic value to 21‐gene and 70‐gene signatures in estrogen receptor‐positive disease
title_full_unstemmed Programmed death‐ligand 1 gene expression is a prognostic marker in early breast cancer and provides additional prognostic value to 21‐gene and 70‐gene signatures in estrogen receptor‐positive disease
title_short Programmed death‐ligand 1 gene expression is a prognostic marker in early breast cancer and provides additional prognostic value to 21‐gene and 70‐gene signatures in estrogen receptor‐positive disease
title_sort programmed death ligand 1 gene expression is a prognostic marker in early breast cancer and provides additional prognostic value to 21 gene and 70 gene signatures in estrogen receptor positive disease
topic breast cancer
gene expression
gene signatures
PD‐L1
prognosis
url https://doi.org/10.1002/1878-0261.12654
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