Racial distribution of molecularly classified brain tumors

Author:

Fang Camila S1ORCID,Wang Wanyi2,Schroff Chanel1,Movahed-Ezazi Misha1ORCID,Vasudevaraja Varshini1ORCID,Serrano Jonathan1ORCID,Sulman Erik P34ORCID,Golfinos John G35ORCID,Orringer Daniel5ORCID,Galbraith Kristyn1ORCID,Feng Yang2,Snuderl Matija31ORCID

Affiliation:

1. Department of Pathology NYU Langone Health and NYU Grossman School of Medicine , New York, New York , USA

2. Department of Biostatistics, NYU School of Global Public Health , New York, New York , USA

3. Brain and Spine Tumor Center, Laura and Isaac Perlmutter Cancer Center, NYU Langone Health , New York, New York , USA

4. Department of Radiation Oncology, NYU Langone Health and NYU Grossman School of Medicine , New York, New York , USA

5. Department of Neurosurgery, NYU Langone Health and NYU Grossman School of Medicine , New York, New York , USA

Abstract

Abstract Background In many cancers, specific subtypes are more prevalent in specific racial backgrounds. However, little is known about the racial distribution of specific molecular types of brain tumors. Public data repositories lack data on many brain tumor subtypes as well as diagnostic annotation using the current World Health Organization classification. A better understanding of the prevalence of brain tumors in different racial backgrounds may provide insight into tumor predisposition and development, and improve prevention. Methods We retrospectively analyzed the racial distribution of 1709 primary brain tumors classified by their methylation profiles using clinically validated whole genome DNA methylation. Self-reported race was obtained from medical records. Our cohort included 82% White, 10% Black, and 8% Asian patients with 74% of patients reporting their race. Results There was a significant difference in the racial distribution of specific types of brain tumors. Blacks were overrepresented in pituitary adenomas (35%, P < .001), with the largest proportion of FSH/LH subtype. Whites were underrepresented at 47% of all pituitary adenoma patients (P < .001). Glioblastoma (GBM) IDH wild-type showed an enrichment of Whites, at 90% (P < .001), and a significantly smaller percentage of Blacks, at 3% (P < .001). Conclusions Molecularly classified brain tumor groups and subgroups show different distributions among the three main racial backgrounds suggesting the contribution of race to brain tumor development.

Funder

Friedberg Charitable Foundation

Gray Family Foundation

Sohn Conference Foundation

Making Headway Foundation

NIH

Publisher

Oxford University Press (OUP)

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