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Identification of a high‐risk subtype of intestinal‐type Japanese gastric cancer by quantitative measurement of the luminal tumor proportion

BACKGROUND: We hypothesized that the relative proportion of tumor (PoT) at the luminal surface can predict gastric cancer (GC) patient survival. METHODS: We measured the luminal PoT in resection specimens from 231 GC patients with stage II/III disease who had surgery at the Kanagawa Cancer Center, Y...

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Autores principales: Aoyama, Toru, Hutchins, Gordon, Arai, Tomio, Sakamaki, Kentaro, Miyagi, Yohei, Tsuburaya, Akira, Ogata, Takashi, Oshima, Takashi, Earle, Sophie, Yoshikawa, Takaki, Grabsch, Heike I.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6198215/
https://www.ncbi.nlm.nih.gov/pubmed/30160049
http://dx.doi.org/10.1002/cam4.1744
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author Aoyama, Toru
Hutchins, Gordon
Arai, Tomio
Sakamaki, Kentaro
Miyagi, Yohei
Tsuburaya, Akira
Ogata, Takashi
Oshima, Takashi
Earle, Sophie
Yoshikawa, Takaki
Grabsch, Heike I.
author_facet Aoyama, Toru
Hutchins, Gordon
Arai, Tomio
Sakamaki, Kentaro
Miyagi, Yohei
Tsuburaya, Akira
Ogata, Takashi
Oshima, Takashi
Earle, Sophie
Yoshikawa, Takaki
Grabsch, Heike I.
author_sort Aoyama, Toru
collection PubMed
description BACKGROUND: We hypothesized that the relative proportion of tumor (PoT) at the luminal surface can predict gastric cancer (GC) patient survival. METHODS: We measured the luminal PoT in resection specimens from 231 GC patients with stage II/III disease who had surgery at the Kanagawa Cancer Center, Yokohama, Japan. Tissue microarrays were used to assess the extent of immune cell infiltration by CD45 immunohistochemistry. Results were related to histopathological features and patient overall survival (OS). RESULTS: PoT was significantly lower in diffuse‐type (30%) compared to intestinal‐type GC (41%), P = 0.03. Patients with low PoT intestinal‐type GC survived significantly longer than patients with high PoT intestinal‐type GC (5 years OS: 78% vs 47%, P = 0.0112). Low PoT was an independent favorable prognostic factor in multivariate analysis in intestinal‐type GC. Low PoT was correlated with high content of CD45‐positive immune cells (P = 0.035). There was no relationship between PoT and survival in diffuse‐type GC. CONCLUSIONS: This is the first study to identify a subgroup of patients with stage II/III intestinal‐type GC at high risk of recurrence by measuring PoT at the luminal surface. The relationship between PoT and immune cell content provides an initial insight into potential underlying biological mechanisms.
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spelling pubmed-61982152018-10-31 Identification of a high‐risk subtype of intestinal‐type Japanese gastric cancer by quantitative measurement of the luminal tumor proportion Aoyama, Toru Hutchins, Gordon Arai, Tomio Sakamaki, Kentaro Miyagi, Yohei Tsuburaya, Akira Ogata, Takashi Oshima, Takashi Earle, Sophie Yoshikawa, Takaki Grabsch, Heike I. Cancer Med Clinical Cancer Research BACKGROUND: We hypothesized that the relative proportion of tumor (PoT) at the luminal surface can predict gastric cancer (GC) patient survival. METHODS: We measured the luminal PoT in resection specimens from 231 GC patients with stage II/III disease who had surgery at the Kanagawa Cancer Center, Yokohama, Japan. Tissue microarrays were used to assess the extent of immune cell infiltration by CD45 immunohistochemistry. Results were related to histopathological features and patient overall survival (OS). RESULTS: PoT was significantly lower in diffuse‐type (30%) compared to intestinal‐type GC (41%), P = 0.03. Patients with low PoT intestinal‐type GC survived significantly longer than patients with high PoT intestinal‐type GC (5 years OS: 78% vs 47%, P = 0.0112). Low PoT was an independent favorable prognostic factor in multivariate analysis in intestinal‐type GC. Low PoT was correlated with high content of CD45‐positive immune cells (P = 0.035). There was no relationship between PoT and survival in diffuse‐type GC. CONCLUSIONS: This is the first study to identify a subgroup of patients with stage II/III intestinal‐type GC at high risk of recurrence by measuring PoT at the luminal surface. The relationship between PoT and immune cell content provides an initial insight into potential underlying biological mechanisms. John Wiley and Sons Inc. 2018-08-29 /pmc/articles/PMC6198215/ /pubmed/30160049 http://dx.doi.org/10.1002/cam4.1744 Text en © 2018 The Authors. Cancer Medicine published by John Wiley & Sons Ltd. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Clinical Cancer Research
Aoyama, Toru
Hutchins, Gordon
Arai, Tomio
Sakamaki, Kentaro
Miyagi, Yohei
Tsuburaya, Akira
Ogata, Takashi
Oshima, Takashi
Earle, Sophie
Yoshikawa, Takaki
Grabsch, Heike I.
Identification of a high‐risk subtype of intestinal‐type Japanese gastric cancer by quantitative measurement of the luminal tumor proportion
title Identification of a high‐risk subtype of intestinal‐type Japanese gastric cancer by quantitative measurement of the luminal tumor proportion
title_full Identification of a high‐risk subtype of intestinal‐type Japanese gastric cancer by quantitative measurement of the luminal tumor proportion
title_fullStr Identification of a high‐risk subtype of intestinal‐type Japanese gastric cancer by quantitative measurement of the luminal tumor proportion
title_full_unstemmed Identification of a high‐risk subtype of intestinal‐type Japanese gastric cancer by quantitative measurement of the luminal tumor proportion
title_short Identification of a high‐risk subtype of intestinal‐type Japanese gastric cancer by quantitative measurement of the luminal tumor proportion
title_sort identification of a high‐risk subtype of intestinal‐type japanese gastric cancer by quantitative measurement of the luminal tumor proportion
topic Clinical Cancer Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6198215/
https://www.ncbi.nlm.nih.gov/pubmed/30160049
http://dx.doi.org/10.1002/cam4.1744
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