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The European Society of Paediatric Oncology Ependymoma-II program Core-Plus model: Development and initial
S Thomas1, D Reynolds1, M C H J Morrall2
1Department of Paediatric Neuropsychology, Nottingham Children's Hospital, Queen's Medical Centre, Nottingham, NG7 2UH, UK; Child Brain Tumour Research Centre, School of Medicine, University of Nottingham, Queen's Medical Centre, Nottingham, NG7 2UH, UK.
Insights
Childhood brain tumor treatment success now includes quality of survival. A new Core-Plus model standardizes cognitive follow-up for ependymoma survivors, aiding future international research.
Area of Science:
- Pediatric Oncology
- Neuro-oncology
- Clinical Trial Design
Background:
- Childhood brain tumors, particularly ependymomas, require treatment evaluation beyond survival rates.
- Quality of survival is a critical metric for assessing pediatric brain tumor therapies.
- Ependymomas are the third most common pediatric brain tumors, posing significant clinical challenges.
Purpose of the Study:
- To establish an internationally accepted cognitive follow-up test battery for childhood ependymoma survivors.
- To adapt treatment protocols, including lowering the age for focal irradiation in posterior fossa ependymoma.
- To address concerns regarding adverse cognitive outcomes in young children undergoing radiotherapy.
Main Methods:
- Development of the 'Core-Plus' model, a two-tier assessment approach for cognitive follow-up.
- Consensus building among 18 European countries over 10 years through the European Society of Paediatric Oncology Ependymoma II program.
- Incorporation of longitudinal cognitive assessment as an essential trial outcome.
Main Results:
- Achieved European consensus on an internationally accepted test battery for childhood ependymoma survivor follow-up.
- The Core-Plus model offers a flexible approach, balancing core assessments with comprehensive options.
- Identified challenges and learnings from the initial stages of the trial.
Conclusions:
- The Core-Plus model provides a standardized solution for cognitive follow-up in international childhood brain tumor trials.
- This model can be applied to other conditions associated with cognitive morbidity.
- The study emphasizes the importance of quality of survival and cognitive outcomes in pediatric neuro-oncology.
Abstract:
It is increasingly accepted that survival alone is an inadequate measure of the success of childhood brain tumour treatments. Consequently, there is growing emphasis on capturing quality of survival. Ependymomas are the third most frequently occurring brain tumours in childhood and present significant clinical challenges. European Society of Paediatric Oncology Ependymoma II is a comprehensive international program aiming to evaluate outcomes under different treatment regimens and improve diagnostic accuracy. Importantly, there has been agreement to lower the age at which children with posterior fossa ependymoma undergo focal irradiation from three years to either eighteen months or one year of age. Hitherto radiotherapy in Europe had been reserved for children over three years due to concerns over adverse cognitive outcomes following irradiation of the developing brain. There is therefore a duty of care to include longitudinal cognitive follow-up and this has been agreed as an essential trial outcome. Discussions between representatives of 18 participating European countries over 10 years have yielded European consensus for an internationally accepted test battery for follow-up of childhood ependymoma survivors. The 'Core-Plus' model incorporates a two-tier approach to assessment by specifying core tests to establish a minimum dataset where resources are limited, whilst maintaining scope for comprehensive assessment where feasible. The challenges leading to the development of the Core-Plus model are presented alongside learning from the initial stages of the trial. We propose that this model could provide a solution for future international trials addressing both childhood brain tumours and other conditions associated with cognitive morbidity.
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