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Primary tumor inflammation in gross tumor volume as a prognostic factor for nasopharyngeal carcinoma patients
PURPOSE: The objective of this study is to investigate the prognostic value of primary tumor inflammation (PTI) in nasopharyngeal carcinoma (NPC) in the era of intensity-modulated radiation therapy (IMRT). RESULTS: PTI was observed in 376/1708 (22.0%) patients, and was present in the sphenoid sinus...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4924765/ https://www.ncbi.nlm.nih.gov/pubmed/26934649 http://dx.doi.org/10.18632/oncotarget.7699 |
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author | Peng, Hao Chen, Lei Tang, Ling-Long Zhang, Yuan Li, Wen-Fei Mao, Yan-Ping Zhang, Fan Guo, Rui Liu, Li-Zhi Tian, Li Lin, Ai-Hua Sun, Ying Ma, Jun |
author_facet | Peng, Hao Chen, Lei Tang, Ling-Long Zhang, Yuan Li, Wen-Fei Mao, Yan-Ping Zhang, Fan Guo, Rui Liu, Li-Zhi Tian, Li Lin, Ai-Hua Sun, Ying Ma, Jun |
author_sort | Peng, Hao |
collection | PubMed |
description | PURPOSE: The objective of this study is to investigate the prognostic value of primary tumor inflammation (PTI) in nasopharyngeal carcinoma (NPC) in the era of intensity-modulated radiation therapy (IMRT). RESULTS: PTI was observed in 376/1708 (22.0%) patients, and was present in the sphenoid sinus in 289/376 (76.9%), in the nasal cavity in 27 (7.2%), and in both places in 60 (15.9%). The estimated 4-year local relapse-free survival (LRFS), disease-free survival (DFS), overall survival (OS) and distant metastasis-free survival (DMFS) rates for PTI vs. non-PTI group were 89.2% vs. 96.1% (P < 0.001), 73.4% vs. 85.1% (P < 0.001), 85.0% vs. 92.1% (P < 0.001) and 83.6% vs. 91.4% (P < 0.001), respectively. After adjustment for these known prognostic factors, PTI was confirmed as an independent prognostic factor for LRFS (HR 2.152, 95% CI 1.318–3.516, P = 0.002), DFS (HR 1.581, 95% CI 1.204–2.077, P = 0.001) and DMFS (HR 1.682, 95% CI 1.177–2.402, P = 0.004). CONCLUSIONS: Primary tumor inflammation was identified as a strong prognostic factor for patients with NPC in the era of IMRT and should be considered when devising future treatment strategies aimed at improving survival in NPC patients. MATERIALS AND METHODS: Data on 1708 patients with nonmetastatic, histologically-confirmed NPC treated with IMRT between November 2009 and February 2012 at Sun Yat-Sen University Cancer Center were retrospectively reviewed. Patient survival between PTI and non-PTI groups were compared. |
format | Online Article Text |
id | pubmed-4924765 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-49247652016-07-13 Primary tumor inflammation in gross tumor volume as a prognostic factor for nasopharyngeal carcinoma patients Peng, Hao Chen, Lei Tang, Ling-Long Zhang, Yuan Li, Wen-Fei Mao, Yan-Ping Zhang, Fan Guo, Rui Liu, Li-Zhi Tian, Li Lin, Ai-Hua Sun, Ying Ma, Jun Oncotarget Research Paper PURPOSE: The objective of this study is to investigate the prognostic value of primary tumor inflammation (PTI) in nasopharyngeal carcinoma (NPC) in the era of intensity-modulated radiation therapy (IMRT). RESULTS: PTI was observed in 376/1708 (22.0%) patients, and was present in the sphenoid sinus in 289/376 (76.9%), in the nasal cavity in 27 (7.2%), and in both places in 60 (15.9%). The estimated 4-year local relapse-free survival (LRFS), disease-free survival (DFS), overall survival (OS) and distant metastasis-free survival (DMFS) rates for PTI vs. non-PTI group were 89.2% vs. 96.1% (P < 0.001), 73.4% vs. 85.1% (P < 0.001), 85.0% vs. 92.1% (P < 0.001) and 83.6% vs. 91.4% (P < 0.001), respectively. After adjustment for these known prognostic factors, PTI was confirmed as an independent prognostic factor for LRFS (HR 2.152, 95% CI 1.318–3.516, P = 0.002), DFS (HR 1.581, 95% CI 1.204–2.077, P = 0.001) and DMFS (HR 1.682, 95% CI 1.177–2.402, P = 0.004). CONCLUSIONS: Primary tumor inflammation was identified as a strong prognostic factor for patients with NPC in the era of IMRT and should be considered when devising future treatment strategies aimed at improving survival in NPC patients. MATERIALS AND METHODS: Data on 1708 patients with nonmetastatic, histologically-confirmed NPC treated with IMRT between November 2009 and February 2012 at Sun Yat-Sen University Cancer Center were retrospectively reviewed. Patient survival between PTI and non-PTI groups were compared. Impact Journals LLC 2016-02-25 /pmc/articles/PMC4924765/ /pubmed/26934649 http://dx.doi.org/10.18632/oncotarget.7699 Text en Copyright: © 2016 Peng et al. http://creativecommons.org/licenses/by/2.5/ 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 Peng, Hao Chen, Lei Tang, Ling-Long Zhang, Yuan Li, Wen-Fei Mao, Yan-Ping Zhang, Fan Guo, Rui Liu, Li-Zhi Tian, Li Lin, Ai-Hua Sun, Ying Ma, Jun Primary tumor inflammation in gross tumor volume as a prognostic factor for nasopharyngeal carcinoma patients |
title | Primary tumor inflammation in gross tumor volume as a prognostic factor for nasopharyngeal carcinoma patients |
title_full | Primary tumor inflammation in gross tumor volume as a prognostic factor for nasopharyngeal carcinoma patients |
title_fullStr | Primary tumor inflammation in gross tumor volume as a prognostic factor for nasopharyngeal carcinoma patients |
title_full_unstemmed | Primary tumor inflammation in gross tumor volume as a prognostic factor for nasopharyngeal carcinoma patients |
title_short | Primary tumor inflammation in gross tumor volume as a prognostic factor for nasopharyngeal carcinoma patients |
title_sort | primary tumor inflammation in gross tumor volume as a prognostic factor for nasopharyngeal carcinoma patients |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4924765/ https://www.ncbi.nlm.nih.gov/pubmed/26934649 http://dx.doi.org/10.18632/oncotarget.7699 |
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