The plasma Epstein–Barr virus DNA level guides precision treatment for nasopharyngeal carcinoma in the intensity-modulated radiotherapy era: a large population-based cohort study from an endemic area

医学 鼻咽癌 危险系数 内科学 肿瘤科 比例危险模型 倾向得分匹配 养生 置信区间 放射治疗 队列 化疗 人口 生存分析 环境卫生
作者
Hu L,Xing Lv,Lin Wang,Yi‐Shan Wu,Rui Sun,Yan‐Fang Ye,Liangru Ke,Qin Yang,Ya‐Hui Yu,Wen‐Ze Qiu,Guoying Liu,Xin-Jun Huang,Wang‐Zhong Li,Shu‐Hui Lv,Xiang Guo,Yan‐Qun Xiang,Wei‐Xiong Xia
出处
期刊:Therapeutic Advances in Medical Oncology [SAGE Publishing]
卷期号:10 被引量:19
标识
DOI:10.1177/1758835918782331
摘要

In the intensity-modulated radiotherapy (IMRT) era, the survival benefit of concurrent chemotherapy for locoregionally advanced nasopharyngeal carcinoma (LA-NPC) remains undetermined. This study aimed to evaluate the benefits of IMRT with concurrent chemotherapy compared with IMRT alone for LA-NPC patients with different plasma Epstein-Barr virus (EBV) DNA levels.Patients were identified from a prospectively maintained database in an endemic area between November 2002 and December 2013. Cox proportional hazards models, propensity score matching, and inverse probability weighting models were established for survival analysis. Stratification analysis was performed based on interaction effects analysis. Finally, sensitivity analysis was performed considering unmeasured confounders.A total of 1357 eligible patients were enrolled (median follow up 62.4 months; range 3.5-155.8 months). No significant survival differences were observed between groups in the entire cohort. Notably, a significant interaction effect was observed between treatment regimens and EBV DNA levels. In patients with high EBV DNA levels (>4000 copies/ml), all three models showed that IMRT with concurrent chemotherapy significantly improved overall survival [hazard ratio (HR) 2.521, 95% confidence interval (CI) 1.218-5.216], disease-free survival (HR 2.168, 95% CI 1.349-3.483), and distant metastasis-free survival (HR 2.331, 95% CI 1.194-4.551) compared with IMRT alone. No differences were found in patients with low EBV DNA levels. Sensitivity analysis confirmed the robustness of the results.In the IMRT era, concurrent chemotherapy treatment of LA-NPC patients with high EBV DNA levels is reasonable. However, the optimal regimen for LA-NPC patients with low EBV DNA levels needs further validation in randomized clinical trials.

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