Variants in Epithelial-Mesenchymal Transition and Immune Checkpoint Genes Are Associated With Immune Cell Profiles and Predict Survival in Non-Small Cell Lung Cancer.


Journal

Archives of pathology & laboratory medicine
ISSN: 1543-2165
Titre abrégé: Arch Pathol Lab Med
Pays: United States
ID NLM: 7607091

Informations de publication

Date de publication:
01 10 2020
Historique:
accepted: 08 01 2020
pubmed: 10 3 2020
medline: 21 10 2020
entrez: 10 3 2020
Statut: ppublish

Résumé

Identification of gene mutations that are indicative of epithelial-mesenchymal transition and a noninflammatory immune phenotype may be important for predicting response to immune checkpoint inhibitors. To evaluate the utility of multiplex immunofluorescence for immune profiling and to determine the relationships among tumor immune checkpoint and epithelial-mesenchymal transition genomic profiles and the clinical outcomes of patients with nonmetastatic non-small cell lung cancer. Tissue microarrays containing 164 primary tumor specimens from patients with stages I to IIIA non-small cell lung carcinoma were examined by multiplex immunofluorescence and image analysis to determine the expression of programmed death ligand-1 (PD-L1) on malignant cells, CD68+ macrophages, and cells expressing the immune markers CD3, CD8, CD57, CD45RO, FOXP3, PD-1, and CD20. Immune phenotype data were tested for correlations with clinicopathologic characteristics, somatic and germline genetic variants, and outcome. A high percentage of PD-L1+ malignant cells was associated with clinicopathologic characteristics, and high density of CD3+PD-1+ T cells was associated with metastasis, suggesting that these phenotypes may be clinically useful to identify patients who will likely benefit from immunotherapy. We also found that ZEB2 mutations were a proxy for immunologic ignorance and immune tolerance microenvironments and may predict response to checkpoint inhibitors. A multivariate Cox regression model predicted a lower risk of death for patients with a high density of CD3+CD45RO+ memory T cells, carriers of allele G of CTLA4 variant rs231775, and those whose tumors do not have ZEB2 mutations. Genetic variants in epithelial-mesenchymal transition and immune checkpoint genes are associated with immune cell profiles and may predict patient outcomes and response to immune checkpoint blockade.

Identifiants

pubmed: 32150457
pii: 442276
doi: 10.5858/arpa.2019-0419-OA
doi:

Substances chimiques

B7-H1 Antigen 0
Biomarkers, Tumor 0
CD274 protein, human 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1234-1244

Informations de copyright

© 2020 College of American Pathologists.

Auteurs

Edwin Roger Parra (ER)

From the Department of Translational Molecular Pathology, The University of Texas MD Anderson Cancer Center, Houston (Parra, Jiang).

Mei Jiang (M)

From the Department of Translational Molecular Pathology, The University of Texas MD Anderson Cancer Center, Houston (Parra, Jiang).

Juliana Machado-Rugolo (J)

The Department of Pathology and Laboratory of Genomics and Histomorphometry (Machado-Rugolo, Yaegashi, Prieto, Farhat, de Sá, Capelozzi).

Lygia Bertalha Yaegashi (LB)

The Department of Pathology and Laboratory of Genomics and Histomorphometry (Machado-Rugolo, Yaegashi, Prieto, Farhat, de Sá, Capelozzi).

Tabatha Prieto (T)

The Department of Pathology and Laboratory of Genomics and Histomorphometry (Machado-Rugolo, Yaegashi, Prieto, Farhat, de Sá, Capelozzi).

Cecília Farhat (C)

The Department of Pathology and Laboratory of Genomics and Histomorphometry (Machado-Rugolo, Yaegashi, Prieto, Farhat, de Sá, Capelozzi).

Vanessa Karen de Sá (VK)

The Department of Pathology and Laboratory of Genomics and Histomorphometry (Machado-Rugolo, Yaegashi, Prieto, Farhat, de Sá, Capelozzi).
The Department of Oncology, Clinicas Hospital, Faculty of Medicine, São Paulo State University, São Paulo, Brazil (de Sá, Nagai).
The Medical Oncology Department and Translational Immune-Oncology Group, A. C. Camargo Cancer Center, Sã Paulo, Brazil (de Sá, de Lima).

Maria Aparecida Nagai (MA)

The Department of Oncology, Clinicas Hospital, Faculty of Medicine, São Paulo State University, São Paulo, Brazil (de Sá, Nagai).

Vladmir Cláudio Cordeiro de Lima (VCC)

The Medical Oncology Department and Translational Immune-Oncology Group, A. C. Camargo Cancer Center, Sã Paulo, Brazil (de Sá, de Lima).

Tereza Takagaki (T)

The Division of Pneumology, Heart Institute (Incor) (Takagaki), Faculty of Medicine, University of São Paulo, São Paulo, Brazil.

Ricardo Terra (R)

The Department of Thoracic Surgery, Institute of Cancer of São Paulo, São Paulo, Brazil (Terra).
The Department of Thoracic Surgery, Heart Institute (Incor), São Paulo, Brazil (Terra).

Alexandre Todorovic Fabro (AT)

The Department of Pathology and Legal Medicine, Ribeirão Preto School of Medicine, University of São Paulo, Ribeirão Preto, Brazil (Fabro).

Vera Luiza Capelozzi (VL)

The Department of Pathology and Laboratory of Genomics and Histomorphometry (Machado-Rugolo, Yaegashi, Prieto, Farhat, de Sá, Capelozzi).

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