Department of Radiation Oncology, Washington University School of Medicine, Saint Louis, MO, USA.
Saint Louis University School of Medicine, Saint Louis, MO, USA.
Cancer Med. 2018 Aug;7(8):3592-3603. doi: 10.1002/cam4.1626. Epub 2018 Jul 14.
The role of induction chemotherapy in nasopharyngeal carcinoma (NPC) remains controversial. The primary aim of this study was to use the National Cancer Database to evaluate the patterns of care of induction chemotherapy in NPC and its impact on overall survival (OS). Patients with NPC from 2004 to 2014 were obtained from the NCDB. Patients were considered to have received induction chemotherapy if it was started ≥43 days before the start of RT and concurrent CRT if chemotherapy started within 21 days after the start of RT. Propensity score matching was used to control for selection bias. Cox proportional hazards model was used to determine significant predictors of OS. Logistic regression model was used to determine predictors of the use of induction chemotherapy. Significance was defined as a P value <.05. A total of 4857 patients were identified: 4041 patients (87.2%) received concurrent CRT and 816 patients (16.8%) received induction chemotherapy. The use of induction therapy remained stable between 2004 and 2014. Younger patients and those with higher T- and N-stage had a higher likelihood of being treated with induction chemotherapy. The 5-year OS in patients treated with induction chemotherapy and CRT was 66.3% vs 69.1%, respectively (P = .25). There was no difference in OS when these two groups were analyzed after propensity score matching. No differences in OS existed between these treatment groups in patients with T3-T4N1 or TanyN2-3 disease (P = .76). Propensity score matching also did not reveal any difference in OS in patients with T3-T4N1 or TanyN2-3 disease. The use of induction chemotherapy has remained stable in the last decade. In this study of patients with NPC, induction chemotherapy was not associated with improved OS compared to CRT alone.
诱导化疗在鼻咽癌(NPC)中的作用仍存在争议。本研究的主要目的是使用国家癌症数据库评估 NPC 诱导化疗的治疗模式及其对总生存期(OS)的影响。从 NCDB 中获取 2004 年至 2014 年 NPC 患者。如果诱导化疗开始时间距 RT 开始时间≥43 天,且同期放化疗(CRT)中化疗开始时间距 RT 开始时间≤21 天,则认为患者接受了诱导化疗。采用倾向评分匹配法控制选择偏倚。Cox 比例风险模型用于确定 OS 的显著预测因素。采用逻辑回归模型确定诱导化疗使用的预测因素。P 值<.05 为差异有统计学意义。共纳入 4857 例患者:4041 例(87.2%)接受同期 CRT,816 例(16.8%)接受诱导化疗。2004 年至 2014 年期间,诱导化疗的使用率保持稳定。年轻患者和 T、N 分期较高的患者更有可能接受诱导化疗。接受诱导化疗和 CRT 治疗的患者 5 年 OS 分别为 66.3%和 69.1%(P=.25)。经倾向评分匹配后,两组 OS 无差异。在 T3-T4N1 或任何 T 任何 N2-3 疾病患者中,两组 OS 无差异(P=.76)。T3-T4N1 或任何 T 任何 N2-3 疾病患者的倾向评分匹配后 OS 也无差异。在过去十年中,诱导化疗的使用率保持稳定。在这项 NPC 患者研究中,与单独 CRT 相比,诱导化疗并未改善 OS。