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Published on: November 11, 2021
Epidemiology of paediatric central nervous system tumours in Queensland, Australia
Thomas Williams1, Mohammad Naushahi2, Anne Bernard3
1Department of Neurosurgery, Queensland Children's Hospital, Brisbane, Australia; School of Clinical Medicine, University of Queensland, Brisbane, Australia.
Insights
This study analyzed childhood central nervous system (CNS) tumors in Australia, finding pilocytic astrocytoma most common. Shorter symptom intervals were observed in younger children.
Area of Science:
- Pediatric Oncology
- Epidemiology
- Neuro-oncology
Background:
- Limited epidemiologic data exists for pediatric central nervous system (CNS) tumors in Australia.
- Queensland Children's Hospital (QCH) is a key referral center for pediatric CNS tumor cases.
Purpose of the Study:
- To examine the epidemiology of childhood CNS tumors in Australia.
- To determine incidence, common tumor types, locations, and symptom intervals.
Main Methods:
- Retrospective analysis of 221 newly diagnosed pediatric CNS tumors (2015-2019).
- Data collected on patient demographics, histopathology, tumor grade, site, and geography.
- Exclusion of recurrent tumors.
Main Results:
- Incidence ranged from 2.65 to 3.85 cases per 100,000 children.
- Pilocytic astrocytoma was the most frequent tumor, followed by medulloblastoma and Langerhans cell histiocytosis.
- The posterior fossa was the most common tumor location; younger children had shorter symptom intervals.
Conclusions:
- This study provides crucial Australian-specific data on pediatric CNS tumor epidemiology.
- Findings highlight a shorter symptom interval in younger children compared to older ones.
- Pilocytic astrocytoma and posterior fossa tumors are significant in this population.
Abstract:
Within Australia, there is little epidemiologic information regarding paediatric central nervous system (CNS) tumours. This study examined the epidemiology of childhood CNS tumours at Queensland Children's Hospital (QCH), the major paediatric referral centre for Queensland and northern New South Wales. We assessed the data from 221 newly diagnosed childhood CNS tumours across a five-year period from 2015 to 2019. Recurrent tumours were excluded. Data was collected on patient age, gender, histopathological diagnosis, tumour grade, anatomical site, and residential geographical location. The incidence within this period ranged from 2.65 to 3.85 cases per 100,000 children. The median symptom interval was 30 days (IQR 14-122) with presenting features similar to previous studies. The symptom interval was shorter for children zero to three years compared to children four years or older. The most frequent tumour was pilocytic astrocytoma, followed by medulloblastoma and Langerhans cell histiocytosis. The posterior fossa was the most frequent anatomical location for tumours. Our study demonstrated a shorter symptom interval in comparison to previous literature. The study was able to determine the incidence and presenting features within an Australian population.
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