Adult brain tumors in Sub-Saharan Africa: A scoping review

Author:

Kanmounye Ulrick Sidney1ORCID,Karekezi Claire2ORCID,Nyalundja Arsene Daniel13ORCID,Awad Ahmed K14,Laeke Tsegazeab5ORCID,Balogun James A6ORCID

Affiliation:

1. Research Department, Association of Future African Neurosurgeons , Yaounde , Cameroon

2. Neurosurgery Unit, Department of Surgery, Rwanda Military Hospital , Kigali , Rwanda

3. Center for Tropical Diseases and Global Health (CTDGH), Faculty of Medicine, Université Catholique de Bukavu , Bukavu , Democratic Republic of Congo

4. Faculty of Medicine, Ain Shams University , Cairo , Egypt

5. Neurosurgery Unit, Surgery Department, Addis Ababa University, College of Health Sciences , Addis Ababa , Ethiopia

6. Division of Neurosurgery, Department of Surgery, College of Medicine, University of Ibadan , Ibadan , Nigeria

Abstract

Abstract Background Sub-Saharan African (SSA) neuro-oncologists report high workloads and challenges in delivering evidence-based care; however, these reports contrast with modeled estimates of adult neuro-oncology disease burden in the region. This scoping review aimed to better understand the reasons for this discrepancy by mapping out the SSA adult brain tumor landscape based on published literature. Methods Systematic searches were conducted in OVID Medline, Global Index Medicus, African Journals Online, Google Scholar, and faculty of medicine libraries from database inception to May 31, 2021. The results were summarized quantitatively and narratively. English and French peer-reviewed articles were included (title, abstract, and full text). Results Of the 819 records identified, 119 articles by 24 SSA countries (42.9%) were included in the final review. Odeku published the first article in 1967, and nine of the ten most prolific years were in the 21st century. The greatest contributing region was Western Africa (n = 58, 48.7%) led by Nigeria (n = 37, 31.1%). Central Africa had fewer articles published later than the other SSA regions (P = .61). Most studies were nonrandomized (n = 75, 63.0%) and meningiomas (n = 50, 42.0%) were the most common brain tumors reported. Less than 30 studies reported on adjuvant treatment or patient outcomes. Conclusions Most publications were hospital-based, and there was significant heterogeneity in the quality of evidence and reporting. This study highlights the need for rapid and sustainable investments and brain tumor research capacity in SSA.

Publisher

Oxford University Press (OUP)

Subject

Cancer Research,Neurology (clinical),Oncology

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