The association between the tumor immune microenvironments and clinical outcome in low-grade, early-stage endometrial cancer patients.


Journal

The Journal of pathology
ISSN: 1096-9896
Titre abrégé: J Pathol
Pays: England
ID NLM: 0204634

Informations de publication

Date de publication:
12 2022
Historique:
revised: 04 09 2022
received: 18 06 2022
accepted: 21 09 2022
pubmed: 29 9 2022
medline: 11 11 2022
entrez: 28 9 2022
Statut: ppublish

Résumé

Endometrial tumors show substantial heterogeneity in their immune microenvironment. This heterogeneity could be used to improve the accuracy of current outcome prediction tools. We assessed the immune microenvironment of 235 patients diagnosed with low-grade, early-stage endometrial cancer. Multiplex quantitative immunofluorescence was carried out to measure CD8, CD68, FOXP3, PD-1, and PD-L1 markers, as well as cytokeratin (CK), on tissue microarrays. Clustering results revealed five robust immune response patterns, each associated with specific immune populations, cell phenotypes, and cell spatial clustering. Most samples (69%) belonged to the immune-desert subtype, characterized by low immune cell densities. Tumor-infiltrating lymphocyte (TIL)-rich samples (4%) displayed high CD8

Identifiants

pubmed: 36169332
doi: 10.1002/path.6012
pmc: PMC9828119
doi:

Substances chimiques

B7-H1 Antigen 0
Programmed Cell Death 1 Receptor 0
Forkhead Transcription Factors 0
Biomarkers, Tumor 0

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

426-436

Informations de copyright

© 2022 The Authors. The Journal of Pathology published by John Wiley & Sons Ltd on behalf of The Pathological Society of Great Britain and Ireland.

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Auteurs

Álvaro López-Janeiro (Á)

Department of Pathology, Hospital Universitario La Paz, IdiPAZ, Madrid, Spain.

María Villalba-Esparza (M)

Department of Pathology, Clínica Universidad de Navarra, University of Navarra, Pamplona, Spain.
Center for Biomedical Research in the Cancer Network (Centro de Investigación Biomédica en Red de Cáncer, CIBERONC), Instituto de Salud Carlos III, Madrid, Spain.

María Emilia Brizzi (ME)

Department of Pathology, Hospital Universitario La Paz, IdiPAZ, Madrid, Spain.

Daniel Jiménez-Sánchez (D)

Department of Pathology, Clínica Universidad de Navarra, University of Navarra, Pamplona, Spain.

Ignacio Ruz-Caracuel (I)

Department of Pathology, Hospital Universitario Ramón y Cajal, IRYCIS, Madrid, Spain.

Ece Kadioglu (E)

Lunaphore Technologies SA, Tolochenaz, Switzerland.

Ivan Masetto (I)

Akoya Biosciences, Marlborough, MA, USA.

Virginie Goubert (V)

Akoya Biosciences, Marlborough, MA, USA.

David Garcia-Ros (D)

Department of Pathology, Clínica Universidad de Navarra, University of Navarra, Pamplona, Spain.

Ignacio Melero (I)

Center for Biomedical Research in the Cancer Network (Centro de Investigación Biomédica en Red de Cáncer, CIBERONC), Instituto de Salud Carlos III, Madrid, Spain.
Department of Immunology and Immunotherapy, Clínica Universidad de Navarra, Pamplona, Spain.
Program of Immunology and Immunotherapy, CIMA Universidad de Navarra, Pamplona, Spain.

Alberto Peláez-García (A)

Molecular Pathology and Therapeutic Targets Group, La Paz University Hospital (IdiPAZ), Madrid, Spain.

David Hardisson (D)

Department of Pathology, Hospital Universitario La Paz, IdiPAZ, Madrid, Spain.
Center for Biomedical Research in the Cancer Network (Centro de Investigación Biomédica en Red de Cáncer, CIBERONC), Instituto de Salud Carlos III, Madrid, Spain.
Molecular Pathology and Therapeutic Targets Group, La Paz University Hospital (IdiPAZ), Madrid, Spain.
Faculty of Medicine, Universidad Autónoma de Madrid, Madrid, Spain.

Carlos E de Andrea (CE)

Department of Pathology, Clínica Universidad de Navarra, University of Navarra, Pamplona, Spain.
Center for Biomedical Research in the Cancer Network (Centro de Investigación Biomédica en Red de Cáncer, CIBERONC), Instituto de Salud Carlos III, Madrid, Spain.

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