Sun Yat-sen University Cancer Centre, Guangzhou, P. R. China.
State Key Laboratory of Oncology in South China, Guangzhou, P. R. China.
Cancer Med. 2019 Aug;8(9):4214-4225. doi: 10.1002/cam4.2343. Epub 2019 Jun 18.
To ascertain the treatment effect of concurrent chemotherapy (CCT) in stage II-III nasopharyngeal carcinoma (NPC) patients with different Epstein-Barr virus (EBV) DNA level in intensity-modulated radiotherapy (IMRT) era.
A total of 2742 patients diagnosed with stage II-III NPC were involved in this study. Patients received IMRT with/without CCT. Overall survival (OS) was the primary endpoint. Receiver operating characteristics curve was used to determine the cut-off value of pre-DNA based on OS. After propensity score matching, the role of CCT was explored in patients with different EBV DNA level.
In our cohort, the cut-off value of pre EBV DNA was 1460 copies/mL (area under curve [AUC], 0.695-0.769; sensitivity, 0.766; specificity, 0.599). Patients with high EBV DNA level showed poor survival in OS, progression free survival (PFS), locoregional relapse-free survival (LRFS) and distant metastasis-free survival (DMFS). In patients with EBV DNA level >1460 copies/mL, the concurrent chemoradiotherapy (CCRT) group achieved higher 3-year OS compared with IMRT groups. However, the CCRT and IMRT groups showed comparable OS in patients with EBV DNA ≤1460 copies/mL. In multivariate analyses, CCT was a protective factor for OS, PFS, and LRFS in high-risk patients (EBV DNA level >1460 copies/mL), while not an independent prognostic factor among the low-risk patients (EBV DNA level ≤1460 copies/mL).
Pre-EBV DNA could be a useful tool to guide individualized treatment for stage II-III NPC patients. Additional CCT to IMRT improved the survival for patients with high pre-EBV DNA, while those with low pre-EBV DNA could not.
在调强放疗(IMRT)时代,确定不同 EBV DNA 水平的 II-III 期鼻咽癌(NPC)患者同步化疗(CCT)的治疗效果。
本研究共纳入 2742 例诊断为 II-III 期 NPC 的患者。患者接受 IMRT 联合/不联合 CCT。总生存(OS)是主要终点。根据 OS 绘制基于 EBV DNA 的预治疗的受试者工作特征曲线(ROC)以确定截断值。在进行倾向评分匹配后,探讨了 CCT 在不同 EBV DNA 水平患者中的作用。
在我们的队列中,EBV DNA 的预治疗截断值为 1460 拷贝/毫升(AUC,0.695-0.769;敏感性,0.766;特异性,0.599)。高 EBV DNA 水平的患者在 OS、无进展生存(PFS)、局部区域无复发生存(LRFS)和远处转移无复发生存(DMFS)方面的生存较差。在 EBV DNA 水平>1460 拷贝/毫升的患者中,同期放化疗(CCRT)组的 3 年 OS 高于 IMRT 组。然而,在 EBV DNA 水平≤1460 拷贝/毫升的患者中,CCRT 和 IMRT 组的 OS 无差异。多因素分析显示,在高危患者(EBV DNA 水平>1460 拷贝/毫升)中,CCT 是 OS、PFS 和 LRFS 的保护因素,而在低危患者(EBV DNA 水平≤1460 拷贝/毫升)中并非独立的预后因素。
治疗前 EBV DNA 可作为指导 II-III 期 NPC 患者个体化治疗的有用工具。在高 EBV DNA 患者中,IMRT 联合 CCT 可提高生存率,而在低 EBV DNA 患者中则不能。