Pediatric brain tumors in sub-Saharan Africa: a systematic review and meta-analysis

Author:

Nyalundja Arsene Daniel12,Kanmounye Ulrick Sidney2,Karekezi Claire34,Laeke Tsegazeab5,Thango Nqobile67,Balogun James A.8

Affiliation:

1. Center for Tropical Diseases and Global Health (CTDGH), Catholic University of Bukavu, South Kivu, Democratic Republic of Congo;

2. Research Department, Association of Future African Neurosurgeons, Yaoundé, Cameroon;

3. Department of Surgery, Rwanda Military Hospital, Kigali, Rwanda;

4. Department of Surgery, University of Rwanda, Kigali, Rwanda;

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

6. Department of Surgery, University of Cape Town, South Africa;

7. Neuroscience Institute, University of Cape Town, South Africa; and

8. Department of Surgery, College of Medicine, University of Ibadan, Nigeria

Abstract

OBJECTIVE Brain tumors are a global problem, leading to higher cancer-related morbidity and mortality rates in children. Despite the progressive though slow advances in neuro-oncology care, research, and diagnostics in sub-Saharan Africa (SSA), the epidemiological landscape of pediatric brain tumors (PBTs) remains underestimated. This study aimed to systematically analyze the distribution of PBT types in SSA. METHODS Ovid Medline, Global Index Medicus, African Journals Online, Google Scholar, and faculty of medicine libraries were searched for literature on PBTs in SSA published before October 29, 2022. A proportional meta-analysis was performed. RESULTS Forty-nine studies, involving 2360 children, met the inclusion criteria for review; only 20 (40.82%) were included in the quantitative analysis. South Africa and Nigeria were the countries with the most abundant data. Glioma not otherwise specified (NOS) was the common PBT in the 4 SSA regions combined. However, medulloblastoma was more commonly reported in Southern SSA (p = 0.01) than in other regions. The prevalence and the overall pooled proportion of the 3 common PBTs was estimated at 46.27% and 0.41 (95% CI 0.32–0.50, 95% prediction interval [PI] 0.11–0.79), 25.34% and 0.18 (95% CI 0.14–0.21, 95% PI 0.06–0.40), and 12.67% and 0.12 (95% CI 0.09–0.15, 95% PI 0.04–0.29) for glioma NOS, medulloblastoma, and craniopharyngioma, respectively. Sample size moderated the estimated proportion of glioma NOS (p = 0.02). The highest proportion of craniopharyngiomas was in Western SSA, and medulloblastoma and glioma NOS in Central SSA. CONCLUSIONS These findings provide insight into the trends of PBT types and the proportion of the top 3 most common tumors across SSA. Although statistical conclusions are difficult due to the inconsistency in the data, the study identifies critical areas for policy development and collaborations that can facilitate improved outcomes in PBTs in SSA. More accurate epidemiological studies of these tumors are needed to better understand the burden of the disease and the geographic variation in their distribution, and to raise awareness in their subsequent management.

Publisher

Journal of Neurosurgery Publishing Group (JNSPG)

Reference58 articles.

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5. Trends in childhood cancer incidence in sub-Saharan Africa: results from 25 years of cancer registration in Harare (Zimbabwe) and Kyadondo (Uganda);Stoeter O,2021

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