LGG-40. EX VIVO TISSUE METABOLITE PROFILES PREDICT PROGRESSION-FREE SURVIVAL IN PAEDIATRIC CEREBELLAR PILOCYTIC ASTROCYTOMAS. Issue 2 (22nd June 2018)
- Record Type:
- Journal Article
- Title:
- LGG-40. EX VIVO TISSUE METABOLITE PROFILES PREDICT PROGRESSION-FREE SURVIVAL IN PAEDIATRIC CEREBELLAR PILOCYTIC ASTROCYTOMAS. Issue 2 (22nd June 2018)
- Main Title:
- LGG-40. EX VIVO TISSUE METABOLITE PROFILES PREDICT PROGRESSION-FREE SURVIVAL IN PAEDIATRIC CEREBELLAR PILOCYTIC ASTROCYTOMAS
- Authors:
- Bennett, Christopher
Kohe, Sarah
Gill, Simrandip
Ghosh, Neelakshi
Manias, Karen
Oates, Adam
English, Martin
Adamski, Jenny
Tennant, Daniel
Peet, Andrew - Abstract:
- Abstract: Pilocytic astrocytomas are the most common brain tumours arising in children, accounting for ~18% of primary brain tumours. 42% are cerebellar in origin and, whilst they have an excellent 10-year overall survival rate of >90%, progression-free survival for these tumours is variable. Identifying tumours more likely to progress will help determine those requiring more aggressive treatment. Metabolite profiles were obtained from 23 cerebellar pilocytic astrocytomas using High Resolution Magic Angle Spinning NMR (HR-MAS). Cox regression tested the ability of individual metabolites to predict progression-free survival. Progression was defined as the time point at which the local multi-disciplinary team decided to further treat the tumour. Low normalised tissue glutamine concentration was found to be associated with a worse progression-free survival (HR=4.58; P<0.05). Glutamine was found to significantly negatively correlate with glutamate (R 2 =-0.48; P<0.05), suggesting a metabolic link between the metabolites and a mechanism for low glutamine in high-risk tumours. Greater post-surgical residual was associated with poorer progression-free survival (log-rank P<0.05) in this cohort; however, there was no significant correlation between the size of residual tumour and glutamine. This study has shown that metabolite concentrations obtained from tissue samples are associated with progression-free survival of cerebellar pilocytic astrocytoma patients. Low glutamine hasAbstract: Pilocytic astrocytomas are the most common brain tumours arising in children, accounting for ~18% of primary brain tumours. 42% are cerebellar in origin and, whilst they have an excellent 10-year overall survival rate of >90%, progression-free survival for these tumours is variable. Identifying tumours more likely to progress will help determine those requiring more aggressive treatment. Metabolite profiles were obtained from 23 cerebellar pilocytic astrocytomas using High Resolution Magic Angle Spinning NMR (HR-MAS). Cox regression tested the ability of individual metabolites to predict progression-free survival. Progression was defined as the time point at which the local multi-disciplinary team decided to further treat the tumour. Low normalised tissue glutamine concentration was found to be associated with a worse progression-free survival (HR=4.58; P<0.05). Glutamine was found to significantly negatively correlate with glutamate (R 2 =-0.48; P<0.05), suggesting a metabolic link between the metabolites and a mechanism for low glutamine in high-risk tumours. Greater post-surgical residual was associated with poorer progression-free survival (log-rank P<0.05) in this cohort; however, there was no significant correlation between the size of residual tumour and glutamine. This study has shown that metabolite concentrations obtained from tissue samples are associated with progression-free survival of cerebellar pilocytic astrocytoma patients. Low glutamine has previously been associated with worse overall survival in children's brain tumours. Knowledge of a high risk of progression may have altered the clinical management of one patient in our cohort with disease progression. HR-MAS acquires data in minutes and could detect high-risk tumours intraoperatively. … (more)
- Is Part Of:
- Neuro-oncology. Volume 20:Issue 2(2018)supplement 2
- Journal:
- Neuro-oncology
- Issue:
- Volume 20:Issue 2(2018)supplement 2
- Issue Display:
- Volume 20, Issue 2 (2018)
- Year:
- 2018
- Volume:
- 20
- Issue:
- 2
- Issue Sort Value:
- 2018-0020-0002-0000
- Page Start:
- i113
- Page End:
- i113
- Publication Date:
- 2018-06-22
- Subjects:
- Brain Neoplasms -- Periodicals
Brain -- Tumors -- Periodicals
Brain -- Cancer -- Periodicals
Nervous system -- Cancer -- Periodicals
616.99481 - Journal URLs:
- http://neuro-oncology.dukejournals.org/ ↗
http://neuro-oncology.oxfordjournals.org/ ↗
http://www.oxfordjournals.org/content?genre=journal&issn=1522-8517 ↗
http://ukcatalogue.oup.com/ ↗ - DOI:
- 10.1093/neuonc/noy059.381 ↗
- Languages:
- English
- ISSNs:
- 1522-8517
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 6081.288000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 12321.xml