Effects of Epstein-Barr virus viral load and different treatment modality for stage III nasopharyngeal carcinoma

被引:14
作者
Twu, Chih-Wen [1 ]
Wang, Wen-Yi [2 ]
Tsou, Hsiao-Hui [3 ,4 ]
Liu, Yi-Chun [5 ,6 ]
Jiang, Rong-San [7 ]
Liang, Kai-Li [7 ]
Lin, Po-Ju [8 ]
Lin, Tian-Yun [9 ]
Chen, Hsin-Hong [10 ]
Lin, Jin-Ching [5 ,6 ,8 ,10 ]
机构
[1] Changhua Christian Hosp, Dept Otorhinolaryngol, Changhua, Taiwan
[2] Hung Kuang Univ, Dept Nursing, Taichung, Taiwan
[3] Natl Hlth Res Inst, Inst Populat Hlth Sci, Miaoli, Taiwan
[4] China Med Univ, Grad Inst Biostat, Coll Publ Hlth, Taichung, Taiwan
[5] Natl Yang Ming Univ, Inst Clin Med, Sch Med, Taipei, Taiwan
[6] Taichung Vet Gen Hosp, Dept Radiat Oncol, Taichung, Taiwan
[7] Taichung Vet Gen Hosp, Dept Otorhinolaryngol, Taichung, Taiwan
[8] Changhua Christian Hosp, Dept Radiat Oncol, 135 Nanxiao St, Taichung 500, Taiwan
[9] Taipei Vet Gen Hosp, Dept Otorhinolaryngol, Taipei, Taiwan
[10] Changhua Christian Hosp, Div Translat Res, Res Dept, Changhua, Taiwan
来源
HEAD AND NECK-JOURNAL FOR THE SCIENCES AND SPECIALTIES OF THE HEAD AND NECK | 2020年 / 42卷 / 08期
关键词
chemoradiotherapy; Epstein-Barr virus; nasopharyngeal carcinoma; plasma; stage III; PLUS ADJUVANT CHEMOTHERAPY; CONCURRENT CHEMORADIOTHERAPY; RANDOMIZED-TRIAL; PHASE-III; INDUCTION CHEMOTHERAPY; QUANTITATIVE-ANALYSIS; DNA LOAD; RADIOTHERAPY; PLASMA; METAANALYSIS;
D O I
10.1002/hed.26096
中图分类号
R76 [耳鼻咽喉科学];
学科分类号
100213 ;
摘要
Background We investigated treatment results, the effects of different treatment modality, and pretreatment Epstein-Barr virus (EBV) viral load for stage III nasopharyngeal carcinoma (NPC) patients. Methods The initial definitive treatment for 356 stage III NPC patients consisted of concurrent chemoradiotherapy (CCRT) or induction chemotherapy plus radiotherapy (IndCT-RT). The pretreatment EBV DNA level separated patients into a high (n = 106) or low (n = 250) viral load (>= or < 1000 copies/mL) subgroup. Outcome measures include relapse rates and various survivals. Results The 5-year rates of overall survival (OS), progression-free survival (PFS), distant metastasis failure-free survival (DMFFS), and locoregional failure-free survival (LRFFS) were 88.6%, 83.0%, 90.5%, and 90.5%, respectively. Patient characteristics and pretreatment viral load between IndCT-RT and CCRT were no significant differences except for a higher percentage of N2 disease in the IndCT-RT subgroup. Both treatment modality resulted in similar relapse rates (P = .56), OS (P = .20), PFS (P = .53), DMFFS (P = .89), and LRFFS (P = .35). However, patients with a high viral load experienced a higher relapse rate (33.0% vs 12.4%, P < .001) and worse OS (5-year rate, 79.0% vs 92.8%, P < .001), PFS (73.7% vs 88.4%, P < .001), DMFFS (80.2% vs 95.0%, P < .001), and LRFFS (85.6% vs 92.6%, P = .005) than those with a low viral load. Conclusion Long-term treatment results for stage III NPC patients are rather good. IndCT-RT can achieve the same treatment outcome as CCRT. Risk grouping by pretreatment viral load identified a subgroup (30%) of patients associated with a significantly higher relapse rates and worse survivals. These high-risk patients need to strengthen treatment intensity in future trials.
引用
收藏
页码:1765 / 1774
页数:10
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