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Tumour infiltrating lymphocytes correlate with improved survival in patients with esophageal squamous cell carcinoma
We undertook a study of tumour infiltrating lymphocytes (TILs) in a large and relatively homogeneous group of patients with completely resected esophageal squamous cell carcinoma (ESCC). Hematoxylin and eosin–stained sections of 235 ESCC tumours were evaluated for density of TILs in intratumoural (i...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5359661/ https://www.ncbi.nlm.nih.gov/pubmed/28322245 http://dx.doi.org/10.1038/srep44823 |
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author | Jiang, Dongxian Liu, Yalan Wang, Hao Wang, Haixing Song, Qi Sujie, Akesu Huang, Jie Xu, Yifan Zeng, Haiying Tan, Lijie Hou, Yingyong Xu, Chen |
author_facet | Jiang, Dongxian Liu, Yalan Wang, Hao Wang, Haixing Song, Qi Sujie, Akesu Huang, Jie Xu, Yifan Zeng, Haiying Tan, Lijie Hou, Yingyong Xu, Chen |
author_sort | Jiang, Dongxian |
collection | PubMed |
description | We undertook a study of tumour infiltrating lymphocytes (TILs) in a large and relatively homogeneous group of patients with completely resected esophageal squamous cell carcinoma (ESCC). Hematoxylin and eosin–stained sections of 235 ESCC tumours were evaluated for density of TILs in intratumoural (iTIL) and stromal compartments (sTIL). Foxp3+, CD4+, and CD8+ T cells in tumoural and stromal areas were evaluated by immunohistochemistry. Of the 235 tumours, high sTIL (>10%), and iTIL (>10%) were observed in 101 (43.0%) and 98 (41.7%), respectively. The median follow-up period was 36.0 months (95% CI 29.929–42.071). Univariate analysis revealed that sTIL (>10%), iTIL (>20%), vessels involvement, lymph node metastasis, and clinical stage were significantly associated with postoperative outcome. In multivariate analysis, high sTIL (HR: 0.664, P = 0.019 for Disease free survival; HR: 0.608, P = 0.005 for Overall survival) was identified as independent better prognostic factor. Further analysis, sTIL was identified as independently prognostic factor in Stage III-IVa disease, which was not found in Stage I-II disease. Our study demonstrated that sTIL was associated with better ESCC patients’ survival, especially in Stage III-IVa disease. Assessment of sTIL could be useful to discriminate biological behavior for ESCC patients. |
format | Online Article Text |
id | pubmed-5359661 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-53596612017-03-22 Tumour infiltrating lymphocytes correlate with improved survival in patients with esophageal squamous cell carcinoma Jiang, Dongxian Liu, Yalan Wang, Hao Wang, Haixing Song, Qi Sujie, Akesu Huang, Jie Xu, Yifan Zeng, Haiying Tan, Lijie Hou, Yingyong Xu, Chen Sci Rep Article We undertook a study of tumour infiltrating lymphocytes (TILs) in a large and relatively homogeneous group of patients with completely resected esophageal squamous cell carcinoma (ESCC). Hematoxylin and eosin–stained sections of 235 ESCC tumours were evaluated for density of TILs in intratumoural (iTIL) and stromal compartments (sTIL). Foxp3+, CD4+, and CD8+ T cells in tumoural and stromal areas were evaluated by immunohistochemistry. Of the 235 tumours, high sTIL (>10%), and iTIL (>10%) were observed in 101 (43.0%) and 98 (41.7%), respectively. The median follow-up period was 36.0 months (95% CI 29.929–42.071). Univariate analysis revealed that sTIL (>10%), iTIL (>20%), vessels involvement, lymph node metastasis, and clinical stage were significantly associated with postoperative outcome. In multivariate analysis, high sTIL (HR: 0.664, P = 0.019 for Disease free survival; HR: 0.608, P = 0.005 for Overall survival) was identified as independent better prognostic factor. Further analysis, sTIL was identified as independently prognostic factor in Stage III-IVa disease, which was not found in Stage I-II disease. Our study demonstrated that sTIL was associated with better ESCC patients’ survival, especially in Stage III-IVa disease. Assessment of sTIL could be useful to discriminate biological behavior for ESCC patients. Nature Publishing Group 2017-03-21 /pmc/articles/PMC5359661/ /pubmed/28322245 http://dx.doi.org/10.1038/srep44823 Text en Copyright © 2017, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Jiang, Dongxian Liu, Yalan Wang, Hao Wang, Haixing Song, Qi Sujie, Akesu Huang, Jie Xu, Yifan Zeng, Haiying Tan, Lijie Hou, Yingyong Xu, Chen Tumour infiltrating lymphocytes correlate with improved survival in patients with esophageal squamous cell carcinoma |
title | Tumour infiltrating lymphocytes correlate with improved survival in patients with esophageal squamous cell carcinoma |
title_full | Tumour infiltrating lymphocytes correlate with improved survival in patients with esophageal squamous cell carcinoma |
title_fullStr | Tumour infiltrating lymphocytes correlate with improved survival in patients with esophageal squamous cell carcinoma |
title_full_unstemmed | Tumour infiltrating lymphocytes correlate with improved survival in patients with esophageal squamous cell carcinoma |
title_short | Tumour infiltrating lymphocytes correlate with improved survival in patients with esophageal squamous cell carcinoma |
title_sort | tumour infiltrating lymphocytes correlate with improved survival in patients with esophageal squamous cell carcinoma |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5359661/ https://www.ncbi.nlm.nih.gov/pubmed/28322245 http://dx.doi.org/10.1038/srep44823 |
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