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Relationship between the immune microenvironment of different locations in a primary tumour and clinical outcomes of oesophageal squamous cell carcinoma

BACKGROUND: Tumour microenvironments can differ according to intratumoural locations. We investigated the immune status at different locations in primary tumours and its clinical significance in oesophageal squamous cell carcinoma (ESCC). METHODS: The number of CD8(+) tumour-infiltrating immune cell...

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Autores principales: Hatogai, Ken, Fujii, Satoshi, Kitano, Shigehisa, Kojima, Takashi, Daiko, Hiroyuki, Yoshino, Takayuki, Ohtsu, Atsushi, Takiguchi, Yuichi, Doi, Toshihiko, Ochiai, Atsushi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7000821/
https://www.ncbi.nlm.nih.gov/pubmed/31761900
http://dx.doi.org/10.1038/s41416-019-0622-3
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author Hatogai, Ken
Fujii, Satoshi
Kitano, Shigehisa
Kojima, Takashi
Daiko, Hiroyuki
Yoshino, Takayuki
Ohtsu, Atsushi
Takiguchi, Yuichi
Doi, Toshihiko
Ochiai, Atsushi
author_facet Hatogai, Ken
Fujii, Satoshi
Kitano, Shigehisa
Kojima, Takashi
Daiko, Hiroyuki
Yoshino, Takayuki
Ohtsu, Atsushi
Takiguchi, Yuichi
Doi, Toshihiko
Ochiai, Atsushi
author_sort Hatogai, Ken
collection PubMed
description BACKGROUND: Tumour microenvironments can differ according to intratumoural locations. We investigated the immune status at different locations in primary tumours and its clinical significance in oesophageal squamous cell carcinoma (ESCC). METHODS: The number of CD8(+) tumour-infiltrating immune cells (TIICs) and PD-1(+) TIICs, and PD-L1 expression on tumour cells (PD-L1(TC)) were immunohistochemically examined in the surface (Surf), centre (Cent) and invasive front (Inv) of tumours surgically resected from 192 patients with ESCC. RESULTS: The PD-L1(+) rate was lower in Inv than in Cent (12.0% vs. 18.2%, P = 0.012), although the numbers of CD8(+) TIICs and PD-1(+) TIICs were comparable among intratumoural locations. High numbers of CD8(+) and PD-1(+) TIICs and positive PD-L1(TC) were related to better overall survival (OS) only in Surf and Cent (CD8: P = 0.012 in Surf, 0.018 in Cent, and 0.165 in Inv; PD-1: P = 0.028 in Surf, 0.021 in Cent, and 0.208 in Inv; and PD-L1: 0.044 in Surf, 0.026 in Cent, and 0.718 in Inv). Positive PD-L1(TC) in Surf and/or Cent but not in Inv demonstrated a strong tendency toward better OS (P = 0.053). CONCLUSIONS: Immune microenvironments according to the intratumoural location have different effects on the survival of patients with ESCC.
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spelling pubmed-70008212020-11-25 Relationship between the immune microenvironment of different locations in a primary tumour and clinical outcomes of oesophageal squamous cell carcinoma Hatogai, Ken Fujii, Satoshi Kitano, Shigehisa Kojima, Takashi Daiko, Hiroyuki Yoshino, Takayuki Ohtsu, Atsushi Takiguchi, Yuichi Doi, Toshihiko Ochiai, Atsushi Br J Cancer Article BACKGROUND: Tumour microenvironments can differ according to intratumoural locations. We investigated the immune status at different locations in primary tumours and its clinical significance in oesophageal squamous cell carcinoma (ESCC). METHODS: The number of CD8(+) tumour-infiltrating immune cells (TIICs) and PD-1(+) TIICs, and PD-L1 expression on tumour cells (PD-L1(TC)) were immunohistochemically examined in the surface (Surf), centre (Cent) and invasive front (Inv) of tumours surgically resected from 192 patients with ESCC. RESULTS: The PD-L1(+) rate was lower in Inv than in Cent (12.0% vs. 18.2%, P = 0.012), although the numbers of CD8(+) TIICs and PD-1(+) TIICs were comparable among intratumoural locations. High numbers of CD8(+) and PD-1(+) TIICs and positive PD-L1(TC) were related to better overall survival (OS) only in Surf and Cent (CD8: P = 0.012 in Surf, 0.018 in Cent, and 0.165 in Inv; PD-1: P = 0.028 in Surf, 0.021 in Cent, and 0.208 in Inv; and PD-L1: 0.044 in Surf, 0.026 in Cent, and 0.718 in Inv). Positive PD-L1(TC) in Surf and/or Cent but not in Inv demonstrated a strong tendency toward better OS (P = 0.053). CONCLUSIONS: Immune microenvironments according to the intratumoural location have different effects on the survival of patients with ESCC. Nature Publishing Group UK 2019-11-25 2020-02-04 /pmc/articles/PMC7000821/ /pubmed/31761900 http://dx.doi.org/10.1038/s41416-019-0622-3 Text en © The Author(s), under exclusive licence to Cancer Research UK 2019 https://creativecommons.org/licenses/by/4.0/Note: This work is published under the standard license to publish agreement. After 12 months the work will become freely available and the license terms will switch to a Creative Commons Attribution 4.0 International (CC BY 4.0).
spellingShingle Article
Hatogai, Ken
Fujii, Satoshi
Kitano, Shigehisa
Kojima, Takashi
Daiko, Hiroyuki
Yoshino, Takayuki
Ohtsu, Atsushi
Takiguchi, Yuichi
Doi, Toshihiko
Ochiai, Atsushi
Relationship between the immune microenvironment of different locations in a primary tumour and clinical outcomes of oesophageal squamous cell carcinoma
title Relationship between the immune microenvironment of different locations in a primary tumour and clinical outcomes of oesophageal squamous cell carcinoma
title_full Relationship between the immune microenvironment of different locations in a primary tumour and clinical outcomes of oesophageal squamous cell carcinoma
title_fullStr Relationship between the immune microenvironment of different locations in a primary tumour and clinical outcomes of oesophageal squamous cell carcinoma
title_full_unstemmed Relationship between the immune microenvironment of different locations in a primary tumour and clinical outcomes of oesophageal squamous cell carcinoma
title_short Relationship between the immune microenvironment of different locations in a primary tumour and clinical outcomes of oesophageal squamous cell carcinoma
title_sort relationship between the immune microenvironment of different locations in a primary tumour and clinical outcomes of oesophageal squamous cell carcinoma
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7000821/
https://www.ncbi.nlm.nih.gov/pubmed/31761900
http://dx.doi.org/10.1038/s41416-019-0622-3
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