Socioeconomic disparities in survival after high‐risk neuroblastoma treatment with modern therapy

Abstract

BackgroundModern therapeutic advances in high‐risk neuroblastoma have improved overall survival (OS), but it is unclear whether these survival gains have been equitable. This study examined the relationship between socioeconomic status (SES) and overall survival (OS) in children with high‐risk neuroblastoma and whether SES‐associated disparities have changed over time.ProcedureIn this population‐based cohort study, children <18 years diagnosed with high‐risk neuroblastoma (diagnosis at age ≥12 months with metastatic disease) from 1991 to 2015 were identified through the National Cancer Institute’s Surveillance, Epidemiology, and End Results database. Associations of county‐level SES variables and OS were tested with univariate Cox proportional hazards regression. For a subcohort diagnosed after 2007, insurance status was examined as an individual‐level SES variable. Multivariable regression analyses with treatment era and interaction terms were performed when SES variables reached near‐significance (p ≤ .1) in univariate and bivariate modeling with treatment era.ResultsAmong 1217 children, 2‐year OS improved from 53.0 ± 3.4% in 1991–1998 to 76.9 ± 2.9% in 2011–2015 (p < .001). In univariate analyses, children in high‐poverty counties (hazard ratio [HR] = 1.74, 95% confidence interval [CI] = 1.17–2.60, p = .007), and those with Medicaid (HR = 1.40, 95% CI = 1.05–1.86, p = .02) experienced an increased hazard of death. No interactions between treatment era and SES variables were statistically significant in multivariable analyses, indicating that differences in the OS between SES groups did not change over time.ConclusionsSurvival disparities among children with high‐risk neuroblastoma have not widened over time, suggesting equitable access to and benefit from therapeutic advances. However, children of low SES experience persistently inferior survival. Interventions to narrow this disparity are paramount.