Exploring Pediatric Neuroblastoma: A Comprehensive Analysis of Adrenal and Nonadrenal Tumor Characteristics in the United States
Ghaith AlWawi, Mohammad Omar Alrefai, Mohd Zaki Al-Wawi, Asma Qasim, M. Bakri Hammami

TL;DR
This study analyzes survival and characteristics of pediatric neuroblastoma tumors in the U.S., showing adrenal tumors are more aggressive and associated with worse outcomes.
Contribution
The study provides new insights into how tumor location affects survival and characteristics in pediatric neuroblastoma patients.
Findings
Adrenal neuroblastoma is more common in males and younger patients, with higher tumor grade and metastasis at diagnosis.
Nonadrenal neuroblastoma, female sex, surgical resection, and later diagnosis years are linked to better survival outcomes.
Tumor location significantly influences prognosis and treatment approaches in pediatric neuroblastoma.
Abstract
Neuroblastoma (NB) is an aggressive malignant tumor arising from a primitive neural crest origin. While the significance of tumor location in survival outcomes is recognized, it remains inadequately explored. This study provides a comprehensive analysis of the survival and characteristics of pediatric adrenal and nonadrenal NBs in the United States. A retrospective analysis of pediatric primary NB between 1975 and 2016 was conducted using the Surveillance, Epidemiology, and End Results (SEER) database. Univariate and multivariate regression analyses were used to determine prognostic variables. A total of 4,554 patients were included, comprising 52% males ( n = 2,385) and 79.2% Caucasians ( n = 3,569). The median age of the patients was one year (range: 0–19 years). In all, 44.4% ( n = 1,996) of the patients had adrenal NB and 55.6% ( n = 2,496) patients had nonadrenal NB. Adrenal…
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Taxonomy
TopicsNeuroblastoma Research and Treatments · Neuroendocrine Tumor Research Advances · Adrenal and Paraganglionic Tumors
