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Old age at diagnosis increases risk of tumor progression in nasopharyngeal cancer
Age at diagnosis has been found to be a prognostic factor of outcomes in various cancers. However, the effect of age at diagnosis on nasopharyngeal cancer (NPC) progression has not been explored. We retrospectively evaluated the relationship between age and disease progression in 3,153 NPC patients...
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/PMC5323224/ https://www.ncbi.nlm.nih.gov/pubmed/27463012 http://dx.doi.org/10.18632/oncotarget.10818 |
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author | Xie, Jing-Dun Chen, Fu He, Yao-Xuan Chen, Xiao-Di Zhang, Guo-Ye Li, Zhi-Kun Hong, Jing Xie, Dan Cai, Mu-Yan |
author_facet | Xie, Jing-Dun Chen, Fu He, Yao-Xuan Chen, Xiao-Di Zhang, Guo-Ye Li, Zhi-Kun Hong, Jing Xie, Dan Cai, Mu-Yan |
author_sort | Xie, Jing-Dun |
collection | PubMed |
description | Age at diagnosis has been found to be a prognostic factor of outcomes in various cancers. However, the effect of age at diagnosis on nasopharyngeal cancer (NPC) progression has not been explored. We retrospectively evaluated the relationship between age and disease progression in 3,153 NPC patients who underwent radiotherapy, chemotherapy, or chemoradiotherapy between 2007 and 2009. Patients were randomly assigned to either a testing cohort or a validation cohort by computer-generated random assignment. X-tile plots determined the optimal cut-point of age based on survival status to be ≤61 vs. >61 years. Further correlation analysis showed that age >61 years was significantly correlated with the tumor progression and therapeutic regimen in both testing and validation cohorts (P <0.05). In the present study, we observed that older age (>61 years) was a strong and independent predictor of poor disease-free survival (DFS) and cancer-specific survival (CSS), in both univariate and multivariate analyses. Age was also found to be a significant prognostic predictor as well (P <0.05) when evaluating patients with the same disease stage. ROC analysis confirmed the predictive value of age on NPC-specific survival in both cohorts (P <0.001) and suggested that age may improve the ability to discriminate outcomes in NPCs, especially regarding tumor progression. In conclusion, our study suggests that older age at NPC diagnosis is associated with a higher incidence of tumor progression and cancer-specific mortality. Age is a strong and independent predictor of poor outcomes and may allow for more tailored therapeutic decision-making and individualized patient counseling. |
format | Online Article Text |
id | pubmed-5323224 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-53232242017-03-23 Old age at diagnosis increases risk of tumor progression in nasopharyngeal cancer Xie, Jing-Dun Chen, Fu He, Yao-Xuan Chen, Xiao-Di Zhang, Guo-Ye Li, Zhi-Kun Hong, Jing Xie, Dan Cai, Mu-Yan Oncotarget Clinical Research Paper Age at diagnosis has been found to be a prognostic factor of outcomes in various cancers. However, the effect of age at diagnosis on nasopharyngeal cancer (NPC) progression has not been explored. We retrospectively evaluated the relationship between age and disease progression in 3,153 NPC patients who underwent radiotherapy, chemotherapy, or chemoradiotherapy between 2007 and 2009. Patients were randomly assigned to either a testing cohort or a validation cohort by computer-generated random assignment. X-tile plots determined the optimal cut-point of age based on survival status to be ≤61 vs. >61 years. Further correlation analysis showed that age >61 years was significantly correlated with the tumor progression and therapeutic regimen in both testing and validation cohorts (P <0.05). In the present study, we observed that older age (>61 years) was a strong and independent predictor of poor disease-free survival (DFS) and cancer-specific survival (CSS), in both univariate and multivariate analyses. Age was also found to be a significant prognostic predictor as well (P <0.05) when evaluating patients with the same disease stage. ROC analysis confirmed the predictive value of age on NPC-specific survival in both cohorts (P <0.001) and suggested that age may improve the ability to discriminate outcomes in NPCs, especially regarding tumor progression. In conclusion, our study suggests that older age at NPC diagnosis is associated with a higher incidence of tumor progression and cancer-specific mortality. Age is a strong and independent predictor of poor outcomes and may allow for more tailored therapeutic decision-making and individualized patient counseling. Impact Journals LLC 2016-07-24 /pmc/articles/PMC5323224/ /pubmed/27463012 http://dx.doi.org/10.18632/oncotarget.10818 Text en Copyright: © 2016 Xie 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 | Clinical Research Paper Xie, Jing-Dun Chen, Fu He, Yao-Xuan Chen, Xiao-Di Zhang, Guo-Ye Li, Zhi-Kun Hong, Jing Xie, Dan Cai, Mu-Yan Old age at diagnosis increases risk of tumor progression in nasopharyngeal cancer |
title | Old age at diagnosis increases risk of tumor progression in nasopharyngeal cancer |
title_full | Old age at diagnosis increases risk of tumor progression in nasopharyngeal cancer |
title_fullStr | Old age at diagnosis increases risk of tumor progression in nasopharyngeal cancer |
title_full_unstemmed | Old age at diagnosis increases risk of tumor progression in nasopharyngeal cancer |
title_short | Old age at diagnosis increases risk of tumor progression in nasopharyngeal cancer |
title_sort | old age at diagnosis increases risk of tumor progression in nasopharyngeal cancer |
topic | Clinical Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5323224/ https://www.ncbi.nlm.nih.gov/pubmed/27463012 http://dx.doi.org/10.18632/oncotarget.10818 |
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