Yang Shan-Shan, Guo Jian-Gui, Liu Jia-Ni, Liu Zhi-Qiao, Chen En-Ni, Chen Chun-Yan, OuYang Pu-Yun, Han Fei, Xie Fang-Yun
Department of Radiation Oncology, 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, China.
Department of Radiation Oncology, The First People's Hospital of Foshan, Foshan, China.
Front Oncol. 2021 Jan 8;10:591205. doi: 10.3389/fonc.2020.591205. eCollection 2020.
Previous meta-analysis had evaluated the effect of induction chemotherapy in nasopharyngeal carcinoma. But two trials with opposite findings were not included and the long-term result of another trial significantly differed from the preliminary report. This updated meta-analysis was thus warranted.
Literature search was conducted to identify randomized controlled trials focusing on the additional efficacy of induction chemotherapy in nasopharyngeal carcinoma. Trial-level pooled analysis of hazard ratio (HR) for progression free survival and overall survival and risk ratio (RR) for locoregional control rate and distant control rate were performed.
Twelve trials were eligible. The addition of induction chemotherapy significantly prolonged both progression free survival (HR=0.68, 95% confidence interval [CI] 0.60-0.76, p<0.001) and overall survival (HR=0.67, 95% CI 0.54-0.80, p<0.001), with 5-year absolute benefit of 11.31% and 8.95%, respectively. Locoregional (RR=0.80, 95% CI 0.70-0.92, p=0.002) and distant control (RR=0.70, 95% CI 0.62-0.80) rates were significantly improved as well. The incidence of grade 3-4 adverse events during the concurrent chemoradiotherapy was higher in leukopenia (p=0.028), thrombocytopenia (p<0.001), and fatigue (p=0.038) in the induction chemotherapy group.
This meta-analysis supported that induction chemotherapy could benefit patients with nasopharyngeal carcinoma in progression free survival, overall survival, locoregional, and distant control rate.
既往的荟萃分析评估了诱导化疗在鼻咽癌中的作用。但两项结果相反的试验未被纳入,且另一项试验的长期结果与初步报告有显著差异。因此有必要进行此次更新的荟萃分析。
进行文献检索以确定关注诱导化疗在鼻咽癌中额外疗效的随机对照试验。对无进展生存期和总生存期的风险比(HR)以及局部区域控制率和远处控制率的风险比(RR)进行试验水平的汇总分析。
12项试验符合条件。添加诱导化疗显著延长了无进展生存期(HR = 0.68,95%置信区间[CI] 0.60 - 0.76,p < 0.001)和总生存期(HR = 0.67,95% CI 0.54 - 0.80,p < 0.001),5年绝对获益分别为11.31%和8.95%。局部区域(RR = 0.80,95% CI 0.70 - 0.92,p = 0.002)和远处控制(RR = 0.70,95% CI 0.62 - 0.80)率也显著提高。诱导化疗组在同步放化疗期间3 - 4级不良事件的发生率在白细胞减少(p = 0.028)、血小板减少(p < 0.001)和疲劳(p = 0.038)方面更高。
这项荟萃分析支持诱导化疗可使鼻咽癌患者在无进展生存期、总生存期、局部区域和远处控制率方面获益。