The value of integrating tumor volume and plasma Epstein-Barr virus DNA load during sequential chemoradiotherapy for prognostic prediction and therapeutic guidance in high-risk locoregionally advanced nasopharyngeal carcinoma

被引:3
作者
Wang, Gaoyuan [1 ]
Dong, Zhe [1 ]
Huang, Chenglong [1 ]
Du, Xiaojing [1 ]
Chen, Lin [1 ]
Li, Kunpeng [1 ]
Guo, Rui [1 ]
Tang, Linglong [1 ]
Ma, Jun [1 ,2 ]
机构
[1] Sun Yat sen Univ, Dept Radiat Oncol, Collaborat Innovat Ctr Canc Med, Canc Ctr,Ctr Precis Med,The State Key Lab Oncol So, Guangzhou, Peoples R China
[2] Sun Yat sen Univ, Dept Radiat Oncol, Collaborat Innovat Ctr Canc, Canc Ctr,Ctr Precis Med,The State Key Lab Oncol So, 651 Dongfeng Rd East, Guangzhou 510060, Peoples R China
基金
中国国家自然科学基金;
关键词
Nasopharyngeal carcinoma; Tumor burden; Epstein -Barr virus infections; Chemoradiotherapy; Adjuvant chemotherapy; INTENSITY-MODULATED RADIOTHERAPY; LYMPH-NODE METASTASIS; ADJUVANT CHEMOTHERAPY;
D O I
10.1016/j.oraloncology.2023.106500
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Objectives: To investigate the value of integrating primary gross tumor volume (GTVp) and gross tumor volume of nodes (GTVn) after induction chemotherapy (IC) and dynamic changes in plasma cell-free Epstein-Barr virus DNA (cfEBV DNA) during sequential chemoradiotherapy (CRT) in high-risk locoregionally advanced nasopharyngeal carcinoma (LA-NPC). Materials and methods: We retrospectively reviewed 988 patients with LA-NPC undergoing IC plus concurrent chemoradiotherapy (CCRT) between 2014 and 2018. The entire cohort was divided into four subgroups according to tumor volume and the cfEBV DNA load. Using a supervised statistical clustering approach, we stratified the subgroups into three clusters. Overall survival (OS), disease-free survival (DFS), distant metastasisfree survival (DMFS) and locoregional relapse-free survival (LRRFS) were calculated using Kaplan-Meier analysis and inter-group differences were compared using the log-rank test. Results: We observed that GTVp & GTVn and cfEBV DNApostIC & cfEBV DNApostCRT were powerful prognostic factors for OS (p = 0.004, p < 0.001, p < 0.001, and p < 0.001, respectively). The survival curves of the three clusters were significantly different. The 5-year OS for the low-risk, intermediate-risk and high-risk clusters were 97.0%, 86.2% and 77.1% (all P values < 0.001), respectively. The risk stratification system showed better predictive performance than the current tumor-node-metastasis (TNM) classification for OS (area under curve [AUC]: 0.653 versus 0.560, p < 0.001), DFS (AUC: 0.639 versus 0.540, p < 0.001), DMFS (AUC: 0.628 versus 0.535, p < 0.001) and LRRFS (AUC: 0.616 versus 0.513, p < 0.001). Conclusion: Both tumor volume and the cfEBV DNA level during sequential CRT are effective prognostic indicators for patients with high-risk LA-NPC. The developed risk stratification system incorporating above factors improved survival prediction and demonstrated potential value in decision-making.
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页数:9
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