Department of Translational Medicine, Herbert Wertheim College of Medicine, Florida International University, Miami, FL 33199, USA.
Department of Public Health, Faculty of Medicine, University of Helsinki, 00014 Helsinki, Finland.
Int J Environ Res Public Health. 2020 Jul 15;17(14):5119. doi: 10.3390/ijerph17145119.
: Conclusive information regarding the influence of race on survival among neuroblastoma patients is limited. Our objective is to investigate the association between race and cause-specific survival in pediatric patients diagnosed with neuroblastoma in the US between 1973 and 2015. : This was a retrospective cohort study using the Surveillance, Epidemiology, and End Result (SEER) database. Patients aged 17 and younger of black, white, or Asian Pacific Islander (API) race diagnosed with neuroblastoma from 1973-2015 were included (n = 2,119). The outcome variable was time from diagnosis to death. Covariates included age, gender, ethnicity, stage, tumor site, and year of diagnosis. Cox proportional hazard models were used to calculate hazard ratios and 95% confidence intervals. : There were no statistically significant differences in the hazard of survival for blacks (HR 0.93; 95% confidence interval (CI) 0.74-1.16) or API (HR 1.02; 95% CI 0.76-1.37) compared with whites. However, patients diagnosed between 2000-2004 (HR 0.46; 95% CI 0.36-0.59) and 2005-2015 (HR 0.33; 95% CI 0.26-0.41) had decreased hazards of death when compared to patients treated during 1973 to 1999. : No association between race and survival time was found. However, survival improved among all patients treated during 2000-2004 and 2005-2015 compared with those treated before the year 2000, leading to a narrowing of the racial disparity based on survival.
种族对神经母细胞瘤患者生存的影响尚无定论信息。本研究旨在调查美国 1973 年至 2015 年间诊断为神经母细胞瘤的儿科患者的种族与特定原因生存之间的关联。
这是一项回顾性队列研究,使用监测、流行病学和最终结果 (SEER) 数据库。纳入年龄在 17 岁及以下、黑种人、白种人或亚太裔(API)种族、1973-2015 年间诊断为神经母细胞瘤的患者(n=2119)。结局变量为从诊断到死亡的时间。协变量包括年龄、性别、种族、分期、肿瘤部位和诊断年份。采用 Cox 比例风险模型计算风险比和 95%置信区间。
与白人相比,黑人(HR 0.93;95%置信区间(CI)0.74-1.16)或 API(HR 1.02;95% CI 0.76-1.37)的生存风险无统计学差异。然而,与 1973 年至 1999 年接受治疗的患者相比,2000-2004 年(HR 0.46;95% CI 0.36-0.59)和 2005-2015 年(HR 0.33;95% CI 0.26-0.41)诊断的患者死亡风险降低。
未发现种族与生存时间之间存在关联。然而,与 2000 年之前接受治疗的患者相比,所有在 2000-2004 年和 2005-2015 年期间接受治疗的患者的生存都有所改善,这导致了基于生存的种族差异缩小。