Long-term incidence of glioma in Olmsted County, Minnesota, and disparities in postglioma survival rate: a population-based study.

astrocytoma glioblastoma mortality pediatric socioeconomic

Journal

Neuro-oncology practice
ISSN: 2054-2577
Titre abrégé: Neurooncol Pract
Pays: England
ID NLM: 101640528

Informations de publication

Date de publication:
Jun 2020
Historique:
entrez: 16 6 2020
pubmed: 17 6 2020
medline: 17 6 2020
Statut: ppublish

Résumé

We assessed glioma incidence and disparities in postglioma survival rate in the Olmsted County, Minnesota, population. This population-based study assessed the incidence of pathologically confirmed primary gliomas between January 1, 1995, and December 31, 2014. Age- and sex-adjusted incidence rates per 100 000 person-years were calculated and standardized to the US white 2010 population. We compared incidence trends of glioma during our study period with previously published Olmsted County data from 1950 to 1990. We assessed postglioma survival rates among individuals with different socioeconomic status (SES), which was measured by a validated individual HOUsing-based SES index (HOUSES). We identified 135 incident glioma cases (93% white) with 20 pediatric (50% female) and 115 adult cases (44% female). Overall incidence rate during our study period, 5.51 per 100 000 person-years (95% CI: 4.56-6.46), showed no significant changes and was similar to that seen in 1950 to 1990, 5.5 per 100 000 person-years. The incidence of pediatric (age < 20 years) glioma was 2.49 (95% CI: 1.40-3.58), whereas adult glioma incidence was 6.47 (95% CI: 5.26-7.67). Among those with grade II to IV gliomas, individuals with lower SES (< median HOUSES) had significantly lower 5-year survival rates compared to those with higher SES, adjusted hazard ratio 1.61 (95% CI: 1.01-2.85). In a well-defined North American population, long-term glioma incidence appears stable since 1950. Significant socioeconomic disparities exist for postglioma survival.

Sections du résumé

BACKGROUND BACKGROUND
We assessed glioma incidence and disparities in postglioma survival rate in the Olmsted County, Minnesota, population.
METHODS METHODS
This population-based study assessed the incidence of pathologically confirmed primary gliomas between January 1, 1995, and December 31, 2014. Age- and sex-adjusted incidence rates per 100 000 person-years were calculated and standardized to the US white 2010 population. We compared incidence trends of glioma during our study period with previously published Olmsted County data from 1950 to 1990. We assessed postglioma survival rates among individuals with different socioeconomic status (SES), which was measured by a validated individual HOUsing-based SES index (HOUSES).
RESULTS RESULTS
We identified 135 incident glioma cases (93% white) with 20 pediatric (50% female) and 115 adult cases (44% female). Overall incidence rate during our study period, 5.51 per 100 000 person-years (95% CI: 4.56-6.46), showed no significant changes and was similar to that seen in 1950 to 1990, 5.5 per 100 000 person-years. The incidence of pediatric (age < 20 years) glioma was 2.49 (95% CI: 1.40-3.58), whereas adult glioma incidence was 6.47 (95% CI: 5.26-7.67). Among those with grade II to IV gliomas, individuals with lower SES (< median HOUSES) had significantly lower 5-year survival rates compared to those with higher SES, adjusted hazard ratio 1.61 (95% CI: 1.01-2.85).
CONCLUSION CONCLUSIONS
In a well-defined North American population, long-term glioma incidence appears stable since 1950. Significant socioeconomic disparities exist for postglioma survival.

Identifiants

pubmed: 32537178
doi: 10.1093/nop/npz065
pii: npz065
pmc: PMC7274190
doi:

Types de publication

Journal Article

Langues

eng

Pagination

288-298

Subventions

Organisme : NIA NIH HHS
ID : R01 AG034676
Pays : United States
Organisme : NHLBI NIH HHS
ID : R01 HL126667
Pays : United States

Informations de copyright

© The Author(s) 2019. Published by Oxford University Press on behalf of the Society for Neuro-Oncology and the European Association of Neuro-Oncology. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.

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Auteurs

Conor S Ryan (CS)

Department of Neurology, Mayo Clinic, Rochester, MN.

Young J Juhn (YJ)

Department of Pediatrics, Mayo Clinic, Rochester, MN.

Harsheen Kaur (H)

Department of Pediatrics, Mayo Clinic, Rochester, MN.

Chung-Il Wi (CI)

Department of Pediatrics, Mayo Clinic, Rochester, MN.

Euijung Ryu (E)

Department of Health Sciences Research, Mayo Clinic, Rochester, MN.

Katherine S King (KS)

Department of Health Sciences Research, Mayo Clinic, Rochester, MN.

Daniel H Lachance (DH)

Department of Neurology, Mayo Clinic, Rochester, MN.

Classifications MeSH