Influence of county-level geographic/ancestral origin on glioma incidence and outcomes in US Hispanics

Author:

Walsh Kyle M123ORCID,Neff Corey14,Bondy Melissa L5,Kruchko Carol4ORCID,Huse Jason T6ORCID,Amos Christopher I7,Barnholtz-Sloan Jill S48ORCID,Ostrom Quinn T1234ORCID

Affiliation:

1. Department of Neurosurgery, Duke University School of Medicine , Durham, North Carolina , USA

2. The Preston Robert Tisch Brain Tumor Center, Duke University School of Medicine , Durham, NC

3. Duke Cancer Institute, Duke University Medical Center , Durham, North Carolina , USA

4. Central Brain Tumor Registry of the United States , Hinsdale, Illinois , USA

5. Department of Epidemiology and Population Health, Stanford University School of Medicine , Stanford, California , USA

6. Department of Translational Molecular Pathology and Department of Pathology, The University of Texas MD Anderson Cancer Center , Houston, Texas , USA

7. Department of Medicine, Section of Epidemiology and Population Sciences, and Institute for Clinical and Translational Research, Dan L. Duncan Comprehensive Cancer Center, Baylor College of Medicine , Houston, Texas , USA

8. Center for Biomedical Informatics & Information Technology and Division of Cancer Epidemiology and Genetics, National Cancer Institute , Bethesda, Maryland , USA

Abstract

Abstract Background Glioma incidence is 25% lower in Hispanics than White non-Hispanics. The US Hispanic population is diverse, and registry-based analyses may mask incidence differences associated with geographic/ancestral origins. Methods County-level glioma incidence data in Hispanics were retrieved from the Central Brain Tumor Registry of the United States. American Community Survey data were used to determine the county-level proportion of the Hispanic population of Mexican/Central American and Caribbean origins. Age-adjusted incidence rate ratios and incidence rate ratios (IRRs) quantified the glioma incidence differences across groups. State-level estimates of admixture in Hispanics were obtained from published 23andMe data. Results Compared to predominantly Caribbean-origin counties, predominantly Mexican/Central American-origin counties had lower age-adjusted risks of glioma (IRR = 0.83; P < 0.0001), glioblastoma (IRR = 0.86; P < 0.0001), diffuse/anaplastic astrocytoma (IRR = 0.78; P < 0.0001), oligodendroglioma (IRR = 0.82; P < 0.0001), ependymoma (IRR = 0.88; P = 0.012), and pilocytic astrocytoma (IRR = 0.76; P < 0.0001). Associations were consistent in children and adults and using more granular geographic regions. Despite having lower glioma incidence, Hispanic glioblastoma patients from predominantly Mexican/Central American-origin counties had poorer survival than Hispanics living in predominantly Caribbean-origin counties. Incidence and survival differences could be partially explained by state-level estimates of European admixture in Hispanics with European admixture associated with higher incidence and improved survival. Conclusions Glioma incidence and outcomes differ in association with the geographic origins of Hispanic communities, with counties of predominantly Mexican/Central American origin at significantly reduced risk and those of Caribbean origin at comparatively greater risk. Although typically classified as a single ethnic group, appreciating the cultural, socioeconomic, and genetic diversity of Hispanics can advance cancer disparities research.

Funder

Centers for Disease Control and Prevention

American Brain Tumor Association

Sontag Foundation

Novocure

Musella Foundation

National Brain Tumor Society

Pediatric Brain Tumor Foundation

Uncle Kory Foundation

Zelda Dorin Tetenbaum Memorial Fund

Publisher

Oxford University Press (OUP)

Subject

Cancer Research,Neurology (clinical),Oncology

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