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Tumor‐infiltrating CD8(+) T‐cell density is an independent prognostic marker for oral squamous cell carcinoma
BACKGROUND: The presence of tumor‐infiltrating lymphocytes (TILs) is associated with improved survival in head and neck squamous cell carcinoma. However, the prognostic value of TILs remains unclear in oral squamous cell carcinoma (OSCC). METHODS: We evaluated the associations between tumor‐infiltra...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6346233/ https://www.ncbi.nlm.nih.gov/pubmed/30600646 http://dx.doi.org/10.1002/cam4.1889 |
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author | Shimizu, Shota Hiratsuka, Hiroyoshi Koike, Kazushige Tsuchihashi, Kei Sonoda, Tomoko Ogi, Kazuhiro Miyakawa, Akira Kobayashi, Junichi Kaneko, Takeshi Igarashi, Tomohiro Hasegawa, Tadashi Miyazaki, Akihiro |
author_facet | Shimizu, Shota Hiratsuka, Hiroyoshi Koike, Kazushige Tsuchihashi, Kei Sonoda, Tomoko Ogi, Kazuhiro Miyakawa, Akira Kobayashi, Junichi Kaneko, Takeshi Igarashi, Tomohiro Hasegawa, Tadashi Miyazaki, Akihiro |
author_sort | Shimizu, Shota |
collection | PubMed |
description | BACKGROUND: The presence of tumor‐infiltrating lymphocytes (TILs) is associated with improved survival in head and neck squamous cell carcinoma. However, the prognostic value of TILs remains unclear in oral squamous cell carcinoma (OSCC). METHODS: We evaluated the associations between tumor‐infiltrating CD8(+) T‐cell density and survival in five distinct compartments in 139 OSCC cases. RESULTS: There was a significant association between increased tumor‐infiltrating CD8(+) T cells and their distribution. High parenchymal CD8(+) T‐cell density at the invading tumor edge was associated with improved overall survival (OS) and disease‐specific survival (DSS; P < 0.01 and P < 0.01, respectively). High stromal CD8(+) T‐cell density at the tumor periphery was also associated with improved recurrence‐free survival (RFS; P < 0.01). Cox regression analysis revealed that high stromal CD8(+) T‐cell density at the tumor periphery and high parenchymal CD8(+) T‐cell density at the invading edge were independent prognostic makers (hazard ratio: 0.38 and 0.19, 95% confidence interval, 0.18‐0.80 and 0.05‐0.72, P = 0.01 and 0.01, respectively) for RFS and OS, respectively. CONCLUSIONS: Assessment of CD8(+) T cells at the parenchyma of the invading edge and peripheral stroma provides an indicator of tumor recurrence and prognosis. |
format | Online Article Text |
id | pubmed-6346233 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-63462332019-01-29 Tumor‐infiltrating CD8(+) T‐cell density is an independent prognostic marker for oral squamous cell carcinoma Shimizu, Shota Hiratsuka, Hiroyoshi Koike, Kazushige Tsuchihashi, Kei Sonoda, Tomoko Ogi, Kazuhiro Miyakawa, Akira Kobayashi, Junichi Kaneko, Takeshi Igarashi, Tomohiro Hasegawa, Tadashi Miyazaki, Akihiro Cancer Med Clinical Cancer Research BACKGROUND: The presence of tumor‐infiltrating lymphocytes (TILs) is associated with improved survival in head and neck squamous cell carcinoma. However, the prognostic value of TILs remains unclear in oral squamous cell carcinoma (OSCC). METHODS: We evaluated the associations between tumor‐infiltrating CD8(+) T‐cell density and survival in five distinct compartments in 139 OSCC cases. RESULTS: There was a significant association between increased tumor‐infiltrating CD8(+) T cells and their distribution. High parenchymal CD8(+) T‐cell density at the invading tumor edge was associated with improved overall survival (OS) and disease‐specific survival (DSS; P < 0.01 and P < 0.01, respectively). High stromal CD8(+) T‐cell density at the tumor periphery was also associated with improved recurrence‐free survival (RFS; P < 0.01). Cox regression analysis revealed that high stromal CD8(+) T‐cell density at the tumor periphery and high parenchymal CD8(+) T‐cell density at the invading edge were independent prognostic makers (hazard ratio: 0.38 and 0.19, 95% confidence interval, 0.18‐0.80 and 0.05‐0.72, P = 0.01 and 0.01, respectively) for RFS and OS, respectively. CONCLUSIONS: Assessment of CD8(+) T cells at the parenchyma of the invading edge and peripheral stroma provides an indicator of tumor recurrence and prognosis. John Wiley and Sons Inc. 2019-01-01 /pmc/articles/PMC6346233/ /pubmed/30600646 http://dx.doi.org/10.1002/cam4.1889 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 Shimizu, Shota Hiratsuka, Hiroyoshi Koike, Kazushige Tsuchihashi, Kei Sonoda, Tomoko Ogi, Kazuhiro Miyakawa, Akira Kobayashi, Junichi Kaneko, Takeshi Igarashi, Tomohiro Hasegawa, Tadashi Miyazaki, Akihiro Tumor‐infiltrating CD8(+) T‐cell density is an independent prognostic marker for oral squamous cell carcinoma |
title | Tumor‐infiltrating CD8(+) T‐cell density is an independent prognostic marker for oral squamous cell carcinoma |
title_full | Tumor‐infiltrating CD8(+) T‐cell density is an independent prognostic marker for oral squamous cell carcinoma |
title_fullStr | Tumor‐infiltrating CD8(+) T‐cell density is an independent prognostic marker for oral squamous cell carcinoma |
title_full_unstemmed | Tumor‐infiltrating CD8(+) T‐cell density is an independent prognostic marker for oral squamous cell carcinoma |
title_short | Tumor‐infiltrating CD8(+) T‐cell density is an independent prognostic marker for oral squamous cell carcinoma |
title_sort | tumor‐infiltrating cd8(+) t‐cell density is an independent prognostic marker for oral squamous cell carcinoma |
topic | Clinical Cancer Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6346233/ https://www.ncbi.nlm.nih.gov/pubmed/30600646 http://dx.doi.org/10.1002/cam4.1889 |
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