Pediatric low-grade glioma in Africa: a baseline study before the implementation of Global Initiative for Childhood Cancer strategies.
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Date
2025Author
van Heerden, Jaques
Esterhuizen, Tonya Marianna
Jbebli, Elhem
Fedhila, Faten
Rhayem, Samar
Chabchoub, Imène
Togo, Boubacar
Van Zyl, Anel
Neethling, Beverley
Thomas, Karla
Charlton, Robyn
Ngcana, Thandeka
Naidu, Gita
du Plessis, Jan
Nyeko, Richard
Balagadde-Kambugu, Joyce
Hessissen, Laila
Zeyad, Abdel Aziz
Gamal, Aya
Amany, Mohamed Ali
Hamdy, Rana
Asfour, Hosam Y.
Elayadi, Moatasem
Geel, Jennifer
Parkes, Jeannette
Davidson, Alan
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Show full item recordAbstract
Introduction: Pediatric low-grade glioma (LGG) is a World Health Organization
(WHO) Global Initiative for Childhood Cancer (GICC) index tumor constituting
up to a third of pediatric central nervous system (CNS) tumors. The
baseline characteristics, survival, and management resources for pediatric LGG in Africa are unknown. We aimed to evaluate the pediatric neuro-
oncology multidisciplinary team resources, epidemiology, and survival outcomes
of pediatric LGG in Africa to document baseline information prior to
GICC implementation.
Methods: The study consisted of two parts: a survey completed by
African pediatric oncology units (POU) to evaluate the local resources and a
retrospective evaluation of data to determine the 5-year overall survival (OS)
for patients under 18 years diagnosed with LGG between 2008 and 2018. Data
were described in frequencies and percentages. Survival was expressed with
Kaplan–Meier curves.
Results: Five-hundred and eighty-eight patients were included from fifteen
POUs in six countries: South Africa (45.9%), Egypt (30.8%), Morocco (12.6%),
Mali (4.4%), Tunisia (3.6%) and Uganda (2.7%). The median age was 4.4 years
(interquartile range 2.4–7.3 years). The most common primary tumor site was
the brainstem (n = 125, 21.3%), the most common histology was pilocytic
astrocytoma (n = 270, 47.5%), the majority of tumors (n = 292, 93%) were
localized, and 40 (6.8%) patients had neurofibromatosis. Complete resection was
obtained in 99 (16.8%) cases, incomplete resection in 179 (30.4%), and no surgery
or biopsy only was performed in 310 (52.7%) cases. One hundred and forty-
seven (25.3%) of the 580 patients with a documented radiotherapy status, were
irradiated, and 320 (54.4%) received chemotherapy. Only 259 (15.3%) patients
received chemotherapy of which the most common chemotherapy regimen was
vincristine-carboplatin (n = 220, 84.9%). The 5-year OS was 90.5% ± 1.6%. The 5-
year OS in Tunisia was 95.1% ± 1.1%, 92.4% ± 2.1% in Egypt, 89.0% ± 3.2% in South
Africa, 70.7% ± 6.7% in Morocco and 66.7% ± 15.7% in Uganda (p < 0.001). Four
of the 41 (9.8%) responding countries reported having pediatric neuro-oncology
subspecialists, and four (9.8%) had national pediatric LGG protocols. In Africa
there is one radiotherapy center per 2,235,125 children and one neurosurgeon
per 304,685 children, with ∼70% of these resources accessible in four countries.
Discussion: Due to several resource challenges and developing treatment
centers, only fifteen pediatric oncology units from six countries participated.
We documented a baseline 5-year OS of 94.9% for LGG in African children.
To obtain an accurate estimation of pediatric LGG survival in Africa, increasing
participation from a wider range of countries, especially poorly resourced
settings, is necessary.
KEYWORDS
Africa, low-grade glioma, children, outcomes, systems, GICC
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