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Programmed cell death-ligand 1 expression predicts survival in patients with gastric carcinoma with microsatellite instability

Programmed death-ligand 1 (PD-L1) is expressed in a subgroup of gastric cancers that may benefit from immunotherapy. Microsatellite instability-high (MSI-H) is a potential predictive factor for response to immunotherapy targeting the PD-1 or its ligand PD-L1. The relationship between PD-L1 expressio...

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Autores principales: Cho, Junhun, Lee, Jeeyun, Bang, Heejin, Kim, Seung Tae, Park, Se Hoon, An, Ji Yeong, Choi, Min Gew, Lee, Joon Ho, Sohn, Tae Sung, Bae, Jae Moon, Kang, Won Ki, Kim, Sung, Kim, Kyoung-Mee
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5355099/
https://www.ncbi.nlm.nih.gov/pubmed/28076847
http://dx.doi.org/10.18632/oncotarget.14519
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author Cho, Junhun
Lee, Jeeyun
Bang, Heejin
Kim, Seung Tae
Park, Se Hoon
An, Ji Yeong
Choi, Min Gew
Lee, Joon Ho
Sohn, Tae Sung
Bae, Jae Moon
Kang, Won Ki
Kim, Sung
Kim, Kyoung-Mee
author_facet Cho, Junhun
Lee, Jeeyun
Bang, Heejin
Kim, Seung Tae
Park, Se Hoon
An, Ji Yeong
Choi, Min Gew
Lee, Joon Ho
Sohn, Tae Sung
Bae, Jae Moon
Kang, Won Ki
Kim, Sung
Kim, Kyoung-Mee
author_sort Cho, Junhun
collection PubMed
description Programmed death-ligand 1 (PD-L1) is expressed in a subgroup of gastric cancers that may benefit from immunotherapy. Microsatellite instability-high (MSI-H) is a potential predictive factor for response to immunotherapy targeting the PD-1 or its ligand PD-L1. The relationship between PD-L1 expression and MSI-H status remains poorly understood. In this study, we investigated PD-L1 expression in patients with MSI-H gastric cancer. We analyzed PD-L1 expression in 78 MSI-H gastric cancer tissue samples using immunohistochemistry. PD-L1 expression was classified as expression on tumor cells or on immune cells. We observed PD-L1 expression in 48 gastric cancer samples (61.5%), consisting of 7 (9.0%) cases with tumor PD-L1 expression and 47 (60.3%) cases with immune cell PD-L1 expression. Immune cell PD-L1 expression was frequently associated with intestinal type cancer by the Lauren classification (p = 0.015), with a lower risk of lymph node metastasis (p = 0.027) and lower tumor stages (p = 0.029) compared to MSI-H gastric cancers without PD-L1 expression. Moreover, immune cell PD-L1 expression was an independent favorable prognostic factor for overall survival (versus PD-L1 negative; hazard ratio, 3.451; 95% confidence interval, 1.172–12.745; p = 0.025). In MSI-H gastric cancer, PD-L1 expression was observed to be independently associated with a longer survival.
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spelling pubmed-53550992017-04-15 Programmed cell death-ligand 1 expression predicts survival in patients with gastric carcinoma with microsatellite instability Cho, Junhun Lee, Jeeyun Bang, Heejin Kim, Seung Tae Park, Se Hoon An, Ji Yeong Choi, Min Gew Lee, Joon Ho Sohn, Tae Sung Bae, Jae Moon Kang, Won Ki Kim, Sung Kim, Kyoung-Mee Oncotarget Research Paper Programmed death-ligand 1 (PD-L1) is expressed in a subgroup of gastric cancers that may benefit from immunotherapy. Microsatellite instability-high (MSI-H) is a potential predictive factor for response to immunotherapy targeting the PD-1 or its ligand PD-L1. The relationship between PD-L1 expression and MSI-H status remains poorly understood. In this study, we investigated PD-L1 expression in patients with MSI-H gastric cancer. We analyzed PD-L1 expression in 78 MSI-H gastric cancer tissue samples using immunohistochemistry. PD-L1 expression was classified as expression on tumor cells or on immune cells. We observed PD-L1 expression in 48 gastric cancer samples (61.5%), consisting of 7 (9.0%) cases with tumor PD-L1 expression and 47 (60.3%) cases with immune cell PD-L1 expression. Immune cell PD-L1 expression was frequently associated with intestinal type cancer by the Lauren classification (p = 0.015), with a lower risk of lymph node metastasis (p = 0.027) and lower tumor stages (p = 0.029) compared to MSI-H gastric cancers without PD-L1 expression. Moreover, immune cell PD-L1 expression was an independent favorable prognostic factor for overall survival (versus PD-L1 negative; hazard ratio, 3.451; 95% confidence interval, 1.172–12.745; p = 0.025). In MSI-H gastric cancer, PD-L1 expression was observed to be independently associated with a longer survival. Impact Journals LLC 2017-01-05 /pmc/articles/PMC5355099/ /pubmed/28076847 http://dx.doi.org/10.18632/oncotarget.14519 Text en Copyright: © 2017 Cho et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Paper
Cho, Junhun
Lee, Jeeyun
Bang, Heejin
Kim, Seung Tae
Park, Se Hoon
An, Ji Yeong
Choi, Min Gew
Lee, Joon Ho
Sohn, Tae Sung
Bae, Jae Moon
Kang, Won Ki
Kim, Sung
Kim, Kyoung-Mee
Programmed cell death-ligand 1 expression predicts survival in patients with gastric carcinoma with microsatellite instability
title Programmed cell death-ligand 1 expression predicts survival in patients with gastric carcinoma with microsatellite instability
title_full Programmed cell death-ligand 1 expression predicts survival in patients with gastric carcinoma with microsatellite instability
title_fullStr Programmed cell death-ligand 1 expression predicts survival in patients with gastric carcinoma with microsatellite instability
title_full_unstemmed Programmed cell death-ligand 1 expression predicts survival in patients with gastric carcinoma with microsatellite instability
title_short Programmed cell death-ligand 1 expression predicts survival in patients with gastric carcinoma with microsatellite instability
title_sort programmed cell death-ligand 1 expression predicts survival in patients with gastric carcinoma with microsatellite instability
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5355099/
https://www.ncbi.nlm.nih.gov/pubmed/28076847
http://dx.doi.org/10.18632/oncotarget.14519
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