Childhood Brain Tumours Flashcards

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1
Q

There has been steady improvement in overall survival of children with cancer but not CNS tumours - what is the survival rate?

A

Only 50%

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2
Q

What are the challenges involved in childhood brain tumours?

A
  • Optimisation and individualisation of current therapies
  • Maximise efficacy
  • Minimise side effects
  • Development of new therapeutic approaches
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3
Q

The complexity of CNS tumours involves interaction of what factors?

A
  • Age of onset
  • Location/surgical accessibility
  • Histological type and grade
  • Post surgical stage
  • Biology
  • Impact of treatment
  • Drug resistance
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4
Q

What are some of the issues associated with CNS tumours?

A
  • Brain tumours are relatively rare therefore there is poor understanding of disease biology
  • No accurate disease stratification results in broadly based treatment strategies and high mortality/morbidity
  • Low priority for molecular research results in lack of molecular targets for new treatment approaches
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5
Q

How do we improve outcomes through biology in childhood brain tumours?

A
  1. Markers for patient management leading to validation/clinical trials leading to patient stratification leading to individualised therapy based on biological data
  2. Targets for therapeutic intervention leading to mechanistic studies evaluating the biological role leading to drug development, clinical trials and new rationally developed therapies
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6
Q

What are some of the key genetic hypotheses that have been proven for childhood CNS tumours?

A
  • Genetic markers can predict outcome (e.g. TrkC in medulloblastoma)
  • tumours arising in different anatomical locations are genetically distinct entities
  • tumours arising in different age groups have distinct genetic aberrations
  • tumours of different histological grade have distinct genetic fingerprints
  • development of large datasets linked to clinical parameters will enable discovery of novel therapeutic targets
  • Tumourigenesis arises from disordered neural development and involves distinct tumour specific pathways
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