Identifying optimal candidates for induction chemotherapy among stage II-IVa nasopharyngeal carcinoma based on pretreatment Epstein-Barr virus DNA and nodal maximal standard uptake values of [18F]-fluorodeoxyglucose positron emission tomography

被引:3
作者
Xie, Hao-Jun [1 ,2 ]
Yu, Yi-Fei [3 ]
Sun, Xue-Song [1 ,2 ]
Jia, Guo-Dong [1 ,2 ]
Luo, Dong-Hua [1 ,2 ]
Sun, Rui [1 ,2 ]
Liu, Li-Ting [1 ,2 ]
Guo, Shan-Shan [1 ,2 ]
Liu, Sai-Lan [1 ,2 ]
Chen, Qiu-Yan [1 ,2 ]
Tang, Lin-Quan [1 ,2 ]
Mai, Hai-Qiang [1 ,2 ]
机构
[1] Sun Yat Sen Univ, Collaborat Innovat Ctr Canc Med, Guangdong Key Lab Nasopharyngeal Carcinoma Diag &, Canc Ctr,State Key Lab Oncol South China, Guangzhou, Peoples R China
[2] Sun Yat Sen Univ, Dept Nasopharyngeal Carcinoma, Canc Ctr, 651 Dongfeng Rd East, Guangzhou 510060, Peoples R China
[3] Sun Yat Sen Univ, Affiliated Hosp 1, Dept Organ Transplant Ctr, Guangzhou, Peoples R China
基金
中国国家自然科学基金;
关键词
Epstein– Barr virus (EBV) DNA; induction chemotherapy; nasopharyngeal carcinoma; survival; SUVmax; DISTANT METASTASIS; SURVIVAL ANALYSIS; RADIOTHERAPY; CHEMORADIOTHERAPY;
D O I
10.1002/cam4.3500
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Objective This study aimed to select optimal candidates benefiting from the addition of induction chemotherapy (IC) to concurrent chemoradiotherapy (CCRT) in stage II-IVa nasopharyngeal carcinoma (NPC) based on Epstein-Barr virus (EBV) DNA and nodal maximal standardized uptake values (SUVmax-N) of [F-18]-fluorodeoxyglucose positron emission tomography. Patients and materials A total of 679 patients diagnosed with stage II-IVa (except N0) NPC were retrospectively included in this study. Overall survival was the primary endpoint. Survival differences between different groups were compared using the log-rank test. The hazard ratio (HR) and 95% confidence interval (CI) were calculated using a multivariable Cox proportional hazards model. Results Both high levels of EBV DNA (>1500 copies/mL) and SUVmax-N (>12.3) indicated worse survival conditions. All patients were divided into low- and high-risk groups based on these two biomarkers. The risk group was an independent prognostic factor in OS, progression-free survival (PFS), and distant metastasis-free survival (DMFS) (all p-values<0.05). The addition of IC to CCRT was associated with survival improvement in OS, PFS, and DMFS in high-risk patients, while no survival difference was found between CCRT and IC+CCRT in low-risk patients. Conclusions Our study can help clinicians select stage II-IVa NPC patients who benefit from IC, which is important in guiding individual treatment.
引用
收藏
页码:8852 / 8863
页数:12
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