Jin Ya-Nan, Yao Ji-Jin, Wang Si-Yang, Zhang Wang-Jian, Zhang Fan, Zhou Guan-Qun, Cheng Zhi-Bin, Mo Hao-Yuan, Sun Ying
State Key Laboratory of Oncology in South, China; Collaborative Innovation Center of Cancer Medicine; Department of Nasopharyngeal Carcinoma, Sun Yat-sen University Cancer Center, 651 Dongfeng East Road, Guangzhou, Guangdong 510060, China.
Department of Radiation Oncology, The Fifth Affiliated Hospital of Sun Yat-sen University, Zhuhai, Guangdong 519001, China.
Transl Oncol. 2017 Aug;10(4):527-534. doi: 10.1016/j.tranon.2017.03.007. Epub 2017 May 29.
To assess the effect of adding neoadjuvant chemotherapy (NACT) to concurrent chemoradiotherapy (CCRT) in patients with locoregionally advanced nasopharyngeal carcinoma (NPC) and undetectable pretreatment Epstein-Barr virus (pEBV) DNA.
We enrolled 639 NPC patients with stage II to IVB and undetectable pEBV DNA to receive CCRT with or without NACT. Radiotherapy was 2.0 to 2.27 Gy per fraction with five daily fractions per week for 6 to 7 weeks to the primary tumor and 62 to 70 Gy to the involved neck area. NACT was cisplatin (80-100 mg/mday 1) and 5-fluorouracil (800-1000 mg/m, 120-hour continuous intravenous infusion) every 3 weeks for two or three cycles. CCRT was cisplatin (80-100 mg/mday 1) every 3 weeks for three cycles.
For all patients, the 5-year overall survival (OS), locoregional relapse-free survival (LRFS), distant metastasis-free survival (DMFS), and progression-free survival (PFS) rates were 91.9%, 92.2%, 95.0%, and 86.4%, respectively. There was no significant difference in OS (5-year OS 90.8% [NACT + CCRT group] vs 92.7% [CCRT alone]; hazard ratio [HR] 1.24; P=.486), LRFS (HR 1.13, 95% confidence interval [CI] 0.59-2.14, P=.715), DMFS (HR 0.78, 95% CI 0.34-1.78, P=.554), or PFS (HR 1.21, 95% CI 0.75-1.95, P=.472).
CCRT with or without NACT produced a good treatment outcome in patients with locoregionally advanced NPC and undetectable pEBV DNA, but NACT before CCRT did not significantly improve survival rates.
评估在局部晚期鼻咽癌(NPC)且治疗前爱泼斯坦-巴尔病毒(pEBV)DNA检测不到的患者中,新辅助化疗(NACT)联合同步放化疗(CCRT)的效果。
我们纳入了639例II至IVB期且pEBV DNA检测不到的NPC患者,接受有或无NACT的CCRT。放疗剂量为每次2.0至2.27 Gy,每周5次,持续6至7周,给予原发肿瘤62至70 Gy,累及颈部区域62至70 Gy。NACT为顺铂(80 - 100 mg/m²,第1天)和5-氟尿嘧啶(800 - 1000 mg/m²,120小时持续静脉输注),每3周进行两个或三个周期。CCRT为顺铂(80 - 100 mg/m²,第1天),每3周进行三个周期。
所有患者的5年总生存率(OS)、局部区域无复发生存率(LRFS)、远处转移无复发生存率(DMFS)和无进展生存率(PFS)分别为91.9%、92.2%、95.0%和86.4%。OS(5年OS:NACT + CCRT组为90.8%,单纯CCRT组为92.7%;风险比[HR] 1.24;P = 0.486)、LRFS(HR 1.13,95%置信区间[CI] 0.59 - 2.14,P = 0.715)、DMFS(HR 0.78,95% CI 0.34 - 1.78,P = 0.554)或PFS(HR 1.21,95% CI 0.75 - 1.95,P = 0.472)均无显著差异。
对于局部晚期NPC且pEBV DNA检测不到的患者,无论有无NACT的CCRT均产生了良好的治疗效果,但CCRT前的NACT并未显著提高生存率。