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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2016
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.
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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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