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HGG-17. Novel Fusion in Congenital Brainstem Diffuse High-Grade Glioma
BACKGROUND: Infant-type hemispheric glioma, previously termed infantile glioblastoma multiforme, is a rare infantile neoplasm with improved survival and distinct molecular features when compared to other pediatric and adult-type high-grade glioma. Infant-type high-grade gliomas are typically located...
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/PMC9165180/ http://dx.doi.org/10.1093/neuonc/noac079.232 |
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author | Norris, Gregory Donson, Andrew Milgrom, Sarah Gaskell, Alisa Willard, Nicholas Foreman, Nicholas Gilani, Ahmed Dahl, Nathan |
author_facet | Norris, Gregory Donson, Andrew Milgrom, Sarah Gaskell, Alisa Willard, Nicholas Foreman, Nicholas Gilani, Ahmed Dahl, Nathan |
author_sort | Norris, Gregory |
collection | PubMed |
description | BACKGROUND: Infant-type hemispheric glioma, previously termed infantile glioblastoma multiforme, is a rare infantile neoplasm with improved survival and distinct molecular features when compared to other pediatric and adult-type high-grade glioma. Infant-type high-grade gliomas are typically located in the cerebral hemispheres and are characterized by ALK, ROS1, MET, and NTRK fusions. Typical brainstem gliomas (diffuse midline glioma, H3 K27-altered or diffuse intrinsic pontine glioma) are comparatively rare in this age group. As a result, the biology of brainstem congenital high-grade gliomas is poorly described. RESULTS: A 3 month old female who initially presented with failure to thrive had an apneic event and was found to have an infiltrative mass in the medulla with expansion into the pons and cervical spine on magnetic resonance imaging. She underwent surgical biopsy with pathology revealing diffuse high-grade glioma, WHO grade 4. Next generation sequencing showed no alterations to H3F3A, IDH, or fusions involving BRAF, ALK, ROS1, MET, or NTRK. Whole-transcriptome sequencing revealed a novel fusion of PDGFRB:APOBEC3C. She received chemotherapy with 2 cycles of carboplatin/etoposide and 2 cycles of carboplatin/etoposide/imatinib before having disease progression. She then underwent palliative radiation (35 Gy in 10 fractions) with near complete regression of her disease. Surprisingly, our patient has not had any progression of disease or new lesions now two years from her last therapy. CONCLUSION: Congenital high-grade glioma is a rare, unique entity that greatly differs from its adult and childhood counterparts. Here, we discuss a previously-unreported fusion of PDGFB:APOBEC3C in a patient with congenital brainstem diffuse high-grade glioma with a favorable clinical course. This highlights the importance of routine molecular characterization, both to better understand the complex biology of this rare disease and to guide prognosis and clinical decision making for individual patients and families. |
format | Online Article Text |
id | pubmed-9165180 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-91651802022-06-05 HGG-17. Novel Fusion in Congenital Brainstem Diffuse High-Grade Glioma Norris, Gregory Donson, Andrew Milgrom, Sarah Gaskell, Alisa Willard, Nicholas Foreman, Nicholas Gilani, Ahmed Dahl, Nathan Neuro Oncol High Grade Glioma BACKGROUND: Infant-type hemispheric glioma, previously termed infantile glioblastoma multiforme, is a rare infantile neoplasm with improved survival and distinct molecular features when compared to other pediatric and adult-type high-grade glioma. Infant-type high-grade gliomas are typically located in the cerebral hemispheres and are characterized by ALK, ROS1, MET, and NTRK fusions. Typical brainstem gliomas (diffuse midline glioma, H3 K27-altered or diffuse intrinsic pontine glioma) are comparatively rare in this age group. As a result, the biology of brainstem congenital high-grade gliomas is poorly described. RESULTS: A 3 month old female who initially presented with failure to thrive had an apneic event and was found to have an infiltrative mass in the medulla with expansion into the pons and cervical spine on magnetic resonance imaging. She underwent surgical biopsy with pathology revealing diffuse high-grade glioma, WHO grade 4. Next generation sequencing showed no alterations to H3F3A, IDH, or fusions involving BRAF, ALK, ROS1, MET, or NTRK. Whole-transcriptome sequencing revealed a novel fusion of PDGFRB:APOBEC3C. She received chemotherapy with 2 cycles of carboplatin/etoposide and 2 cycles of carboplatin/etoposide/imatinib before having disease progression. She then underwent palliative radiation (35 Gy in 10 fractions) with near complete regression of her disease. Surprisingly, our patient has not had any progression of disease or new lesions now two years from her last therapy. CONCLUSION: Congenital high-grade glioma is a rare, unique entity that greatly differs from its adult and childhood counterparts. Here, we discuss a previously-unreported fusion of PDGFB:APOBEC3C in a patient with congenital brainstem diffuse high-grade glioma with a favorable clinical course. This highlights the importance of routine molecular characterization, both to better understand the complex biology of this rare disease and to guide prognosis and clinical decision making for individual patients and families. Oxford University Press 2022-06-03 /pmc/articles/PMC9165180/ http://dx.doi.org/10.1093/neuonc/noac079.232 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 | High Grade Glioma Norris, Gregory Donson, Andrew Milgrom, Sarah Gaskell, Alisa Willard, Nicholas Foreman, Nicholas Gilani, Ahmed Dahl, Nathan HGG-17. Novel Fusion in Congenital Brainstem Diffuse High-Grade Glioma |
title | HGG-17. Novel Fusion in Congenital Brainstem Diffuse High-Grade Glioma |
title_full | HGG-17. Novel Fusion in Congenital Brainstem Diffuse High-Grade Glioma |
title_fullStr | HGG-17. Novel Fusion in Congenital Brainstem Diffuse High-Grade Glioma |
title_full_unstemmed | HGG-17. Novel Fusion in Congenital Brainstem Diffuse High-Grade Glioma |
title_short | HGG-17. Novel Fusion in Congenital Brainstem Diffuse High-Grade Glioma |
title_sort | hgg-17. novel fusion in congenital brainstem diffuse high-grade glioma |
topic | High Grade Glioma |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9165180/ http://dx.doi.org/10.1093/neuonc/noac079.232 |
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