Lv Jia-Wei, Chen Yu-Pei, Zhou Guan-Qun, Tang Ling-Long, Mao Yan-Ping, Li Wen-Fei, Guo Rui, Lin Ai-Hua, Ma Jun, Sun Ying
Department of Radiation Oncology, Sun Yat-sen University Cancer Center, State Key Laboratory of Oncology in South China, Collaborative Innovation Center for Cancer Medicine, Guangzhou, People's Republic of China.
Department of Medical Statistics and Epidemiology, School of Public Health, Sun Yat-sen University, Guangzhou, People's Republic of China.
Oncotarget. 2016 Mar 29;7(13):16806-17. doi: 10.18632/oncotarget.7609.
We evaluated the combined prognostic value of cigarette smoking and baseline plasma Epstein-Barr virus deoxyribonucleic acid (EBV DNA) in patients with nasopharyngeal carcinoma (NPC) treated with intensity-modulated radiation therapy (IMRT). Of consecutive patients, 1501 with complete data were eligible for retrospective analysis. Smoking index (SI; cigarette packs per day times smoking duration [years]), was used to evaluate the cumulative effect of smoking. Primary end-point was overall survival (OS); progression-free survival (PFS), distant metastasis-free survival (DMFS) and locoregional relapse-free survival (LRFS) were secondary end-points. Both cigarette smoking and baseline plasma EBV DNA load were associated with poorer survival (P <0.001). Patients were divided into four groups: low EBV DNA and light smoker (LL), low EBV DNA and heavy smoker (LH), high EBV DNA and light smoker (HL), and high EBV DNA and heavy smoker (HH). The respective 5-year survival rates were: OS (93.1%, 87.2%, 82.9%, and 76.3%, P<0.001), PFS (87.0%, 84.0%, 73.9%, and 64.6%, P<0.001), DMFS (94.1%, 92.1%, 82.4%, and72.5%, P<0.001), and LRFS (92.8%, 92.4%, 88.7%, and 84.0%, P=0.012).OS and PFS were significantly different between the LH and HL groups and HL and HH groups, but not LL and LH groups (pairwise comparisons). The combined risk stratification remained an independent prognostic factor for all endpoints (all Ptrend<0.001; multivariate analysis). Both cigarette smoking and baseline plasma EBV DNA were independent prognostic factors for survival outcomes. Combined interpretation of EBV DNA with smoking led to the refinement of the risks stratification for patient subsets, especially with improved risk discrimination in patients with high baseline plasma EBV DNA.
我们评估了吸烟与基线血浆爱泼斯坦-巴尔病毒脱氧核糖核酸(EBV DNA)对接受调强放射治疗(IMRT)的鼻咽癌(NPC)患者的联合预后价值。在连续的患者中,1501例有完整数据的患者符合回顾性分析条件。吸烟指数(SI;每天吸烟包数×吸烟持续时间[年])用于评估吸烟的累积效应。主要终点是总生存期(OS);无进展生存期(PFS)、无远处转移生存期(DMFS)和无局部区域复发生存期(LRFS)为次要终点。吸烟和基线血浆EBV DNA载量均与较差的生存率相关(P<0.001)。患者分为四组:低EBV DNA且轻度吸烟者(LL)、低EBV DNA且重度吸烟者(LH)、高EBV DNA且轻度吸烟者(HL)和高EBV DNA且重度吸烟者(HH)。各自的5年生存率分别为:OS(93.1%、87.2%、82.9%和76.3%,P<0.001)、PFS(87.0%、84.0%、73.9%和64.6%,P<0.001)、DMFS(94.1%、92.1%、82.4%和72.5%,P<0.001)和LRFS(92.8%、92.4%、88.7%和84.0%,P=0.012)。LH组与HL组以及HL组与HH组之间的OS和PFS有显著差异,但LL组与LH组之间无显著差异(两两比较)。联合风险分层仍然是所有终点的独立预后因素(所有Ptrend<0.001;多变量分析)。吸烟和基线血浆EBV DNA都是生存结局的独立预后因素。EBV DNA与吸烟的联合解读导致患者亚组风险分层的细化,特别是在基线血浆EBV DNA高的患者中改善了风险区分。