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LGG-09. A Nationwide Service Evaluation of Safety, Radiologic and Visual Outcome Refining Bevacizumab-based Treatments in Children with Progressive Low-Grade Glioma
INTRODUCTION: Bevacizumab/Irinotecan is currently 3rd-line treatment in the UK for progressive Paediatric Low-Grade Glioma (PLGG) based on limited evidence. A nationwide service evaluation was conducted to review its safety and efficacy amongst a larger cohort. METHODS: Data from children with PLGG...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9164923/ http://dx.doi.org/10.1093/neuonc/noac079.325 |
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author | Green, Katherine Panagopoulou, Paraskevi D’Arco, Felice O'Hare, Patricia Bowman, Richard Walters, Bronwen Dahl, Christine Jorgensen, Mette Patel, Pritesh Slater, Olga Ahmed, Rehana Bailey, Simon Carceller, Fernando Collins, Rhiannon Corley, Elizabeth English, Martin Hayden, James Howells, Lisa Kamal, Ahmed Kilday, John Paul Lowis, Stephen Lumb, Blanche Micic, Thomas Mitra, Dip Pace, Erika Picton, Susan Pizer, Barry Shafiq, Ayad Uzunova, Lena Wilson, Shaun Wayman, Harriet Hargrave, Darren Opocher, Enrico |
author_facet | Green, Katherine Panagopoulou, Paraskevi D’Arco, Felice O'Hare, Patricia Bowman, Richard Walters, Bronwen Dahl, Christine Jorgensen, Mette Patel, Pritesh Slater, Olga Ahmed, Rehana Bailey, Simon Carceller, Fernando Collins, Rhiannon Corley, Elizabeth English, Martin Hayden, James Howells, Lisa Kamal, Ahmed Kilday, John Paul Lowis, Stephen Lumb, Blanche Micic, Thomas Mitra, Dip Pace, Erika Picton, Susan Pizer, Barry Shafiq, Ayad Uzunova, Lena Wilson, Shaun Wayman, Harriet Hargrave, Darren Opocher, Enrico |
author_sort | Green, Katherine |
collection | PubMed |
description | INTRODUCTION: Bevacizumab/Irinotecan is currently 3rd-line treatment in the UK for progressive Paediatric Low-Grade Glioma (PLGG) based on limited evidence. A nationwide service evaluation was conducted to review its safety and efficacy amongst a larger cohort. METHODS: Data from children with PLGG receiving Bevacizumab-based Treatments (BBT) from 11 UK Centres (2009-2020) were reviewed. Radiological and visual outcomes were based on standardized measurements. Clinical-radiological correlation was investigated. Time to progression from BBT stop, progression free-survival (PFS) curves and multivariate analysis of prognostic factors (p 0.05) were performed. RESULTS: 88 children with PLGG (88% OPG, 24% NF1) had BBT for radiological (43%), visual (20%) or combined (27%) progression, after 40 months (median) from diagnosis. Amongst OPG cases, visual acuity (VA) per eye (better/worse) before BBT was logMAR 0.0-0.3 (23/7) 0.3 - 1.0 (27/20), > 1.0 (14/18) and LP/NLP (8/27), with 19/8 children respectively blind (LP/NLP) in one or both eyes. Bevacizumab 10 mg/kg every 14 days (median 24 doses) was given as 3rd line+ with Irinotecan (85%) or alongside 1st/2nd line chemo (15%) leading to remarkable radiological (88%) and visual (74%) responses (stable or improved) within 3-6 months, with limited toxicity. 12% progressed on treatment, and 8% died unrelated to BBT. After initial response 65% progressed at a median of 8 months (4 - 23) after BBT, resulting in 3-year-all-causes-PFS of 16% and 3-yr-visual-PFS of 45% from start of BBT. Visual concordance with MRI was poor (36%) but increases (47%) when better-eye determines visual outcome. Lack of NF1 and diencephalic syndrome (DS) at presentation were independent negative prognostic factors for PFS. CONCLUSIONS: A remarkable but transient effect of BBT has been confirmed. Visual > radiological responses can be sustained after BBT. Variations in current BBT strategies justifies further research, including the potential upfront use alongside conventional first-line chemotherapy as sight-saving strategy. |
format | Online Article Text |
id | pubmed-9164923 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-91649232022-06-05 LGG-09. A Nationwide Service Evaluation of Safety, Radiologic and Visual Outcome Refining Bevacizumab-based Treatments in Children with Progressive Low-Grade Glioma Green, Katherine Panagopoulou, Paraskevi D’Arco, Felice O'Hare, Patricia Bowman, Richard Walters, Bronwen Dahl, Christine Jorgensen, Mette Patel, Pritesh Slater, Olga Ahmed, Rehana Bailey, Simon Carceller, Fernando Collins, Rhiannon Corley, Elizabeth English, Martin Hayden, James Howells, Lisa Kamal, Ahmed Kilday, John Paul Lowis, Stephen Lumb, Blanche Micic, Thomas Mitra, Dip Pace, Erika Picton, Susan Pizer, Barry Shafiq, Ayad Uzunova, Lena Wilson, Shaun Wayman, Harriet Hargrave, Darren Opocher, Enrico Neuro Oncol Low Grade Glioma INTRODUCTION: Bevacizumab/Irinotecan is currently 3rd-line treatment in the UK for progressive Paediatric Low-Grade Glioma (PLGG) based on limited evidence. A nationwide service evaluation was conducted to review its safety and efficacy amongst a larger cohort. METHODS: Data from children with PLGG receiving Bevacizumab-based Treatments (BBT) from 11 UK Centres (2009-2020) were reviewed. Radiological and visual outcomes were based on standardized measurements. Clinical-radiological correlation was investigated. Time to progression from BBT stop, progression free-survival (PFS) curves and multivariate analysis of prognostic factors (p 0.05) were performed. RESULTS: 88 children with PLGG (88% OPG, 24% NF1) had BBT for radiological (43%), visual (20%) or combined (27%) progression, after 40 months (median) from diagnosis. Amongst OPG cases, visual acuity (VA) per eye (better/worse) before BBT was logMAR 0.0-0.3 (23/7) 0.3 - 1.0 (27/20), > 1.0 (14/18) and LP/NLP (8/27), with 19/8 children respectively blind (LP/NLP) in one or both eyes. Bevacizumab 10 mg/kg every 14 days (median 24 doses) was given as 3rd line+ with Irinotecan (85%) or alongside 1st/2nd line chemo (15%) leading to remarkable radiological (88%) and visual (74%) responses (stable or improved) within 3-6 months, with limited toxicity. 12% progressed on treatment, and 8% died unrelated to BBT. After initial response 65% progressed at a median of 8 months (4 - 23) after BBT, resulting in 3-year-all-causes-PFS of 16% and 3-yr-visual-PFS of 45% from start of BBT. Visual concordance with MRI was poor (36%) but increases (47%) when better-eye determines visual outcome. Lack of NF1 and diencephalic syndrome (DS) at presentation were independent negative prognostic factors for PFS. CONCLUSIONS: A remarkable but transient effect of BBT has been confirmed. Visual > radiological responses can be sustained after BBT. Variations in current BBT strategies justifies further research, including the potential upfront use alongside conventional first-line chemotherapy as sight-saving strategy. Oxford University Press 2022-06-03 /pmc/articles/PMC9164923/ http://dx.doi.org/10.1093/neuonc/noac079.325 Text en © The Author(s) 2022. Published by Oxford University Press on behalf of the Society for Neuro-Oncology. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (https://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Low Grade Glioma Green, Katherine Panagopoulou, Paraskevi D’Arco, Felice O'Hare, Patricia Bowman, Richard Walters, Bronwen Dahl, Christine Jorgensen, Mette Patel, Pritesh Slater, Olga Ahmed, Rehana Bailey, Simon Carceller, Fernando Collins, Rhiannon Corley, Elizabeth English, Martin Hayden, James Howells, Lisa Kamal, Ahmed Kilday, John Paul Lowis, Stephen Lumb, Blanche Micic, Thomas Mitra, Dip Pace, Erika Picton, Susan Pizer, Barry Shafiq, Ayad Uzunova, Lena Wilson, Shaun Wayman, Harriet Hargrave, Darren Opocher, Enrico LGG-09. A Nationwide Service Evaluation of Safety, Radiologic and Visual Outcome Refining Bevacizumab-based Treatments in Children with Progressive Low-Grade Glioma |
title | LGG-09. A Nationwide Service Evaluation of Safety, Radiologic and Visual Outcome Refining Bevacizumab-based Treatments in Children with Progressive Low-Grade Glioma |
title_full | LGG-09. A Nationwide Service Evaluation of Safety, Radiologic and Visual Outcome Refining Bevacizumab-based Treatments in Children with Progressive Low-Grade Glioma |
title_fullStr | LGG-09. A Nationwide Service Evaluation of Safety, Radiologic and Visual Outcome Refining Bevacizumab-based Treatments in Children with Progressive Low-Grade Glioma |
title_full_unstemmed | LGG-09. A Nationwide Service Evaluation of Safety, Radiologic and Visual Outcome Refining Bevacizumab-based Treatments in Children with Progressive Low-Grade Glioma |
title_short | LGG-09. A Nationwide Service Evaluation of Safety, Radiologic and Visual Outcome Refining Bevacizumab-based Treatments in Children with Progressive Low-Grade Glioma |
title_sort | lgg-09. a nationwide service evaluation of safety, radiologic and visual outcome refining bevacizumab-based treatments in children with progressive low-grade glioma |
topic | Low Grade Glioma |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9164923/ http://dx.doi.org/10.1093/neuonc/noac079.325 |
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