Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2024 Jan;71(1):e30732.
doi: 10.1002/pbc.30732. Epub 2023 Oct 22.

A comprehensive analysis of neuroblastoma incidence, survival, and racial and ethnic disparities from 2001 to 2019

Affiliations

A comprehensive analysis of neuroblastoma incidence, survival, and racial and ethnic disparities from 2001 to 2019

Kevin Campbell et al. Pediatr Blood Cancer. 2024 Jan.

Abstract

Background: We characterize the incidence and 5-year survival of children and adolescents with neuroblastoma stratified by demographic and clinical factors based on the comprehensive data from United States Cancer Statistics (USCS) and the National Program of Cancer Registries (NPCR).

Methods: We analyzed the incidence of neuroblastoma from USCS (2003-2019) and survival data from NPCR (2001-2018) for patients less than 20 years old. Incidence trends were calculated by average annual percent change (AAPC) using joinpoint regression. Differences in relative survival were estimated comparing non-overlapping confidence intervals (CI).

Results: We identified 11,543 primary neuroblastoma cases in USCS. Age-adjusted incidence was 8.3 per million persons [95% CI: 8.2, 8.5], with an AAPC of 0.4% [95% CI: -0.1, 0.9]. Five-year relative survival from the NPCR dataset (n = 10,676) was 79.7% [95% CI: 78.9, 80.5]. Patients aged less than 1 year had the highest 5-year relative survival (92.5%). Five-year relative survival was higher for non-Hispanic White patients (80.7%) or Hispanic patients (80.8%) compared to non-Hispanic Black patients (72.6%).

Conclusion: Neuroblastoma incidence was stable during 2003-2019. Differences in relative survival exist by sex, age, race/ethnicity, and stage; patients who were male, older, non-Hispanic Black, or with distant disease had worse survival. Future studies could seek to assess the upstream factors driving disparities in survival, and evaluate interventions to address inequities and improve survival across all groups.

Keywords: epidemiology; neuroblastoma; outcomes research.

PubMed Disclaimer

Conflict of interest statement

CONFLICT OF INTEREST STATEMENT

The authors declare they have no conflicts of interest. The findings and conclusions in this report are those of the authors and do not necessarily represent the official position of the Centers for Disease Control and Prevention.

Figures

FIGURE 1
FIGURE 1
Age-adjusted rates per 1,000,000 persons of neuroblastoma/ganglioneuroblastoma diagnosis in the United States from 2003 to 2019.
FIGURE 2
FIGURE 2
Kaplan–Meier 5-year all-cause survival curves of neuroblastoma cases among children and adolescents from the National Program of Cancer Registries (NPCR) database (2001–2018). Data are stratified by (A) age, (B) sex, (C) race and ethnicity, (D) date of diagnosis, (E) stage, (F) histologic type, (G) economic status, and (H) rural–urban status.

References

    1. Siegel DA, King JB, Lupo PJ, et al. Counts, incidence rates, and trends of pediatric cancer in the United States, 2003–2019. J Natl Cance Inst. 2023:djad115. doi:10.1093/jnci/djad115 - DOI - PMC - PubMed
    1. Irwin MS, Naranjo A, Zhang FF, et al. Revised neuroblastoma risk classification system: a report from the Children’s Oncology Group. J Clin Oncol. 2021;39(29):3229–3241. - PMC - PubMed
    1. Sokol E, Desai AV. The evolution of risk classification for neuroblastoma. Children (Basel). 2019;6(2):27. - PMC - PubMed
    1. NIH. Surveillance, epidemiology, and end results (SEER) program SEER*stat database: incidence-SEER 9 regs research data. National Cancer Institute, Surveillance Research Program; 2021.
    1. Cohn SL, Pearson AD, London WB, et al. The International Neuroblastoma Risk Group (INRG) classification system: an INRG Task Force report. J Clin Oncol. 2009;27(2):289–297. - PMC - PubMed