State Key Laboratory of Oncology in South China, Collaborative Innovation Center for Cancer Medicine.
Department of Nasopharyngeal Carcinoma.
J Natl Compr Canc Netw. 2019 Jun 1;17(6):703-710. doi: 10.6004/jnccn.2018.7270.
The goal of this study was to explore the value of adding neoadjuvant chemotherapy (NACT) or adjuvant chemotherapy (ACT) to concurrent chemoradiotherapy (CCRT) in patients with nasopharyngeal carcinoma (NPC) with different risks of treatment failure.
A total of 2,263 eligible patients with stage III-IVb NPC treated with CCRT ± NACT or ACT were included in this retrospective study. Distant metastasis-free survival (DMFS), overall survival, and progression-free survival were calculated using the Kaplan-Meier method and differences were compared using the log-rank test.
Patients in the low-risk group (stage N0-1 disease and Epstein-Barr virus [EBV] DNA <4,000 copies/mL) who received NACT followed by CCRT achieved significantly better 5-year DMFS than those treated with CCRT alone (96.2% vs 91.3%; P= .008). Multivariate analyses also demonstrated that additional NACT was the only independent prognostic factor for DMFS (hazard ratio, 0.42; 95% CI, 0.22-0.80; P=.009). In both the intermediate-risk group (stage N0-1 disease and EBV DNA ≥4,000 copies/mL and stage N2-3 disease and EBV DNA <4,000 copies/mL) and the high-risk group (stage N2-3 disease and EBV DNA ≥4,000 copies/mL), comparison of NACT or ACT + CCRT versus CCRT alone indicated no significantly better survival for all end points.
The addition of NACT to CCRT could reduce distant failure in patients with low risk of treatment failure.
本研究旨在探讨在不同治疗失败风险的鼻咽癌(NPC)患者中,将新辅助化疗(NACT)或辅助化疗(ACT)添加到同期放化疗(CCRT)中的价值。
本回顾性研究共纳入 2263 例接受 CCRT±NACT 或 ACT 治疗的 III-IVb 期 NPC 患者。采用 Kaplan-Meier 法计算无远处转移生存(DMFS)、总生存和无进展生存,采用对数秩检验比较差异。
低危组(N0-1 期疾病和 EBV DNA<4000 拷贝/mL)患者接受 NACT 后再行 CCRT 治疗,5 年 DMFS 显著优于单纯 CCRT 治疗(96.2%比 91.3%;P=.008)。多因素分析也表明,附加 NACT 是 DMFS 的唯一独立预后因素(风险比,0.42;95%可信区间,0.22-0.80;P=.009)。在中危组(N0-1 期疾病和 EBV DNA≥4000 拷贝/mL 和 N2-3 期疾病和 EBV DNA<4000 拷贝/mL)和高危组(N2-3 期疾病和 EBV DNA≥4000 拷贝/mL)中,NACT 或 ACT+CCRT 与单纯 CCRT 相比,所有终点的生存均无显著改善。
在治疗失败风险较低的患者中,将 NACT 添加到 CCRT 中可以降低远处失败的风险。