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ABSTRACT: Background
Neuroblastoma is the most common pediatric extracranial solid tumor. Within conventional risk groups, there is considerable heterogeneity in outcomes, indicating the need for improved risk stratification.Methods
In this study we analyzed the somatic mutational burden of 515 primary, untreated neuroblastoma tumors from three independent cohorts. Mutations in coding regions were determined by whole-exome/genome sequencing of tumor samples compared to matched blood leukocytes. Survival data for 459 patients were available for analysis of 5-year overall survival using the Kaplan-Meier method and log-rank test. All statistical tests were two-sided.Results
Despite a low overall somatic mutational burden (mean = 3, range = 0-56), 107 patients were considered to
SUBMITTER: Hwang WL
PROVIDER: S-EPMC6624164 | biostudies-literature | 2019 Jul
REPOSITORIES: biostudies-literature