Sun Yat-sen University Cancer Center, State Key Laboratory of Oncology in South China, Collaborative Innovation Center for Cancer Medicine, Guangdong Key Laboratory of Nasopharyngeal Carcinoma Diagnosis and Therapy, Guangzhou, P. R. China.
Department of Nasopharyngeal Carcinoma, Sun Yat-sen University Cancer Center, Guangzhou, P. R. China.
Cancer Med. 2020 Dec;9(23):8852-8863. doi: 10.1002/cam4.3500. Epub 2020 Oct 9.
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]-fluorodeoxyglucose positron emission tomography.
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.
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.
Our study can help clinicians select stage II-IVa NPC patients who benefit from IC, which is important in guiding individual treatment.
本研究旨在基于 EBV DNA 和 [F]-氟脱氧葡萄糖正电子发射断层扫描(FDG-PET)的淋巴结最大标准化摄取值(SUVmax-N),选择从诱导化疗(IC)加同期放化疗(CCRT)中获益的 II-IVa 期鼻咽癌(NPC)的最佳候选者。
本研究回顾性纳入了 679 名诊断为 II-IVa(N0 除外)期 NPC 的患者。总生存是主要终点。使用对数秩检验比较不同组之间的生存差异。使用多变量 Cox 比例风险模型计算风险比(HR)和 95%置信区间(CI)。
高水平的 EBV DNA(>1500 拷贝/mL)和 SUVmax-N(>12.3)均提示预后较差。根据这两个生物标志物,所有患者均分为低危和高危组。风险组是 OS、无进展生存(PFS)和无远处转移生存(DMFS)的独立预后因素(均 p<0.05)。高危患者中,IC 加 CCRT 与 OS、PFS 和 DMFS 的生存改善相关,而在低危患者中,CCRT 和 IC+CCRT 之间未发现生存差异。
我们的研究可以帮助临床医生选择从 IC 中获益的 II-IVa 期 NPC 患者,这对于指导个体化治疗非常重要。