Histopathologic and molecular profile of gliomas diagnosed in Lagos, Nigeria

Author:

Odukoya Lateef A1ORCID,Ida Cristiane M1ORCID,Eckel-Passow Jeanette E2,Kollmeyer Thomas M1,Vaubel Rachael1,Lachance Daniel H3,Fonkem Ekokobe4,Badmos Kabir B5,Bankole Olufemi B6,Llewellyn Henry7,Kitange Gasper J8,Aldape Kenneth9ORCID,Daramola Adetola O5,Anunobi Charles C5,Jenkins Robert B1

Affiliation:

1. Department of Laboratory Medicine & Pathology, Mayo Clinic , Rochester, Minnesota   USA

2. Department of Quantitative Health Sciences, Mayo Clinic , Rochester, Minnesota   USA

3. Department of Neurology, Mayo Clinic , Rochester, Minnesota   USA

4. Department of Neurology, Medical College of Wisconsin , Milwaukee, Wisconsin   USA

5. Department of Anatomic and Molecular Pathology, Lagos University Teaching Hospital , Lagos , Nigeria

6. Department of Surgery (Neurosurgery Unit), Lagos University Teaching Hospital , Lagos   Nigeria

7. Department of Global Health & Social Medicine School of Global Affairs King’s College , London

8. The Hormel Institute, University of Minnesota , Austin, Minnesota   USA

9. Laboratory of Pathology National Institutes of Health , Bethesda, Maryland , USA

Abstract

Abstract Background The optimal diagnosis and management of patients with brain tumors currently uses the 2021 WHO integrated diagnosis of histomorphologic and molecular features. However, neuro-oncology practice in resource-limited settings usually relies solely on histomorphology. This study aimed to classify glioma cases diagnosed in the Department of Anatomic and Molecular Pathology, Lagos University Teaching Hospital, using the 2021 WHO CNS tumor classification. Methods Fifty-six brain tumors from 55 patients diagnosed with glioma between 2013 and 2021 were reevaluated for morphologic diagnosis. Molecular features were determined from formalin-fixed paraffin-embedded (FFPE) tissue using immunohistochemistry (IHC) for IDH1-R132H, ATRX, BRAF-V600E, p53, Ki67, and H3-K27M, OncoScan chromosomal microarray for copy number, targeted next generation sequencing for mutation and fusion and methylation array profiling. Results Of 55 central nervous system tumors, 3 were excluded from histomorphologic reevaluation for not being of glial or neuroepithelial origin. Of the remaining 52 patients, the median age was 20.5 years (range: 1 to 60 years), 38(73%) were males and 14(27%) were females. Seventy-one percent of the gliomas evaluated provided adequate DNA from archival FFPE tissue blocks. After applying the 2021 WHO diagnostic criteria the initial morphologic diagnosis changed for 35% (18/52) of cases. Diagnoses of 5 (9.6%) gliomas were upgraded, and 7 (14%) were downgraded. Conclusions This study shows that the incorporation of molecular testing can considerably improve brain tumor diagnoses in Nigeria. Furthermore, this study highlights the diagnostic challenges in resource-limited settings and what is at stake in the global disparities of brain tumor diagnosis.

Funder

National Cancer Institute

National Brain Tumor Society

Publisher

Oxford University Press (OUP)

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