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Induction chemotherapy followed by concurrent chemoradiotherapy versus concurrent chemoradiotherapy alone in stage III-IVb nasopharyngeal carcinoma patients with Epstein-Barr virus DNA ≥4000 copies/ml: a matched study
BACKGROUND: The effects of induction chemotherapy (IC) followed by concurrent chemoradiotherapy (CCRT) in high-risk (stage III-IVb with EBV DNA≥4000 copies/ml) nasopharyngeal carcinoma (NPC) patients are unclear. METHODS: A total of 325 high-risk NPC patients treated with IC+CCRT or CCRT alone who w...
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/PMC5045429/ https://www.ncbi.nlm.nih.gov/pubmed/27105538 http://dx.doi.org/10.18632/oncotarget.8828 |
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author | Guo, Shan-Shan Tang, Lin-Quan Chen, Qiu-Yan Zhang, Lu Liu, Li-Ting Guo, Ling Mo, Hao-Yuan Luo, Dong-Hua Huang, Pei-Yu Xiang, Yan-Qun Sun, Rui Chen, Ming-Yuan Wang, Lin Lv, Xing Zhao, Chong Guo, Xiang Cao, Ka-Jia Qian, Chao-Nan Zeng, Mu-Shen Bei, Jin-Xin Hong, Ming-Huang Shao, Jian-Yong Sun, Ying Ma, Jun Mai, Hai-Qiang |
author_facet | Guo, Shan-Shan Tang, Lin-Quan Chen, Qiu-Yan Zhang, Lu Liu, Li-Ting Guo, Ling Mo, Hao-Yuan Luo, Dong-Hua Huang, Pei-Yu Xiang, Yan-Qun Sun, Rui Chen, Ming-Yuan Wang, Lin Lv, Xing Zhao, Chong Guo, Xiang Cao, Ka-Jia Qian, Chao-Nan Zeng, Mu-Shen Bei, Jin-Xin Hong, Ming-Huang Shao, Jian-Yong Sun, Ying Ma, Jun Mai, Hai-Qiang |
author_sort | Guo, Shan-Shan |
collection | PubMed |
description | BACKGROUND: The effects of induction chemotherapy (IC) followed by concurrent chemoradiotherapy (CCRT) in high-risk (stage III-IVb with EBV DNA≥4000 copies/ml) nasopharyngeal carcinoma (NPC) patients are unclear. METHODS: A total of 325 high-risk NPC patients treated with IC+CCRT or CCRT alone who were treated with intensity-modulated radiation therapy (IMRT) between March 2007 and March 2013 were included. For each patient in the IC+CCRT group, a matched pair in the CCRT group was matching for: gender, age, T stage, N stage, clinical stage and WHO (World Health Organization) type. The primary endpoint was overall survival (OS), and the secondary endpoints were progression-free survival (PFS), distant metastasis-free survival (DMFS), and locoregional relapse-free survival (LRFS). RESULTS: There were no significant differences in OS, PFS, DMFS, and LRFS between the IC+CCRT (148 patients) and CCRT (177 patients) groups. After matching, 103 paired patients were analyzed, and there were no differences between the IC+CCRT and CCRT groups regarding clinical outcomes. Based on the subgroup analysis of 156 very-high-risk patients (stage N2-3 with EBV DNA ≥4000 copies/ml), the 5-year OS of the IC+CCRT and CCRT groups was 84.3% and 67.5% (P =0.033), respectively. Based on our multivariate analysis, the treatment group was significantly associated with OS (P=0.034; HR0.451, 95%CI 0.216-0.941). CONCLUSIONS: IC+CCRT did not improve the clinical outcomes of high-risk NPC patients compared to CCRT alone. However, in very-high-risk patients, IC+CCRT treatment led to increased OS compared to patients received CCRT treatment alone. |
format | Online Article Text |
id | pubmed-5045429 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-50454292016-10-13 Induction chemotherapy followed by concurrent chemoradiotherapy versus concurrent chemoradiotherapy alone in stage III-IVb nasopharyngeal carcinoma patients with Epstein-Barr virus DNA ≥4000 copies/ml: a matched study Guo, Shan-Shan Tang, Lin-Quan Chen, Qiu-Yan Zhang, Lu Liu, Li-Ting Guo, Ling Mo, Hao-Yuan Luo, Dong-Hua Huang, Pei-Yu Xiang, Yan-Qun Sun, Rui Chen, Ming-Yuan Wang, Lin Lv, Xing Zhao, Chong Guo, Xiang Cao, Ka-Jia Qian, Chao-Nan Zeng, Mu-Shen Bei, Jin-Xin Hong, Ming-Huang Shao, Jian-Yong Sun, Ying Ma, Jun Mai, Hai-Qiang Oncotarget Research Paper BACKGROUND: The effects of induction chemotherapy (IC) followed by concurrent chemoradiotherapy (CCRT) in high-risk (stage III-IVb with EBV DNA≥4000 copies/ml) nasopharyngeal carcinoma (NPC) patients are unclear. METHODS: A total of 325 high-risk NPC patients treated with IC+CCRT or CCRT alone who were treated with intensity-modulated radiation therapy (IMRT) between March 2007 and March 2013 were included. For each patient in the IC+CCRT group, a matched pair in the CCRT group was matching for: gender, age, T stage, N stage, clinical stage and WHO (World Health Organization) type. The primary endpoint was overall survival (OS), and the secondary endpoints were progression-free survival (PFS), distant metastasis-free survival (DMFS), and locoregional relapse-free survival (LRFS). RESULTS: There were no significant differences in OS, PFS, DMFS, and LRFS between the IC+CCRT (148 patients) and CCRT (177 patients) groups. After matching, 103 paired patients were analyzed, and there were no differences between the IC+CCRT and CCRT groups regarding clinical outcomes. Based on the subgroup analysis of 156 very-high-risk patients (stage N2-3 with EBV DNA ≥4000 copies/ml), the 5-year OS of the IC+CCRT and CCRT groups was 84.3% and 67.5% (P =0.033), respectively. Based on our multivariate analysis, the treatment group was significantly associated with OS (P=0.034; HR0.451, 95%CI 0.216-0.941). CONCLUSIONS: IC+CCRT did not improve the clinical outcomes of high-risk NPC patients compared to CCRT alone. However, in very-high-risk patients, IC+CCRT treatment led to increased OS compared to patients received CCRT treatment alone. Impact Journals LLC 2016-04-18 /pmc/articles/PMC5045429/ /pubmed/27105538 http://dx.doi.org/10.18632/oncotarget.8828 Text en Copyright: © 2016 Guo 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 Guo, Shan-Shan Tang, Lin-Quan Chen, Qiu-Yan Zhang, Lu Liu, Li-Ting Guo, Ling Mo, Hao-Yuan Luo, Dong-Hua Huang, Pei-Yu Xiang, Yan-Qun Sun, Rui Chen, Ming-Yuan Wang, Lin Lv, Xing Zhao, Chong Guo, Xiang Cao, Ka-Jia Qian, Chao-Nan Zeng, Mu-Shen Bei, Jin-Xin Hong, Ming-Huang Shao, Jian-Yong Sun, Ying Ma, Jun Mai, Hai-Qiang Induction chemotherapy followed by concurrent chemoradiotherapy versus concurrent chemoradiotherapy alone in stage III-IVb nasopharyngeal carcinoma patients with Epstein-Barr virus DNA ≥4000 copies/ml: a matched study |
title | Induction chemotherapy followed by concurrent chemoradiotherapy versus concurrent chemoradiotherapy alone in stage III-IVb nasopharyngeal carcinoma patients with Epstein-Barr virus DNA ≥4000 copies/ml: a matched study |
title_full | Induction chemotherapy followed by concurrent chemoradiotherapy versus concurrent chemoradiotherapy alone in stage III-IVb nasopharyngeal carcinoma patients with Epstein-Barr virus DNA ≥4000 copies/ml: a matched study |
title_fullStr | Induction chemotherapy followed by concurrent chemoradiotherapy versus concurrent chemoradiotherapy alone in stage III-IVb nasopharyngeal carcinoma patients with Epstein-Barr virus DNA ≥4000 copies/ml: a matched study |
title_full_unstemmed | Induction chemotherapy followed by concurrent chemoradiotherapy versus concurrent chemoradiotherapy alone in stage III-IVb nasopharyngeal carcinoma patients with Epstein-Barr virus DNA ≥4000 copies/ml: a matched study |
title_short | Induction chemotherapy followed by concurrent chemoradiotherapy versus concurrent chemoradiotherapy alone in stage III-IVb nasopharyngeal carcinoma patients with Epstein-Barr virus DNA ≥4000 copies/ml: a matched study |
title_sort | induction chemotherapy followed by concurrent chemoradiotherapy versus concurrent chemoradiotherapy alone in stage iii-ivb nasopharyngeal carcinoma patients with epstein-barr virus dna ≥4000 copies/ml: a matched study |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5045429/ https://www.ncbi.nlm.nih.gov/pubmed/27105538 http://dx.doi.org/10.18632/oncotarget.8828 |
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