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MEDB-74. Serial assessment of measurable residual disease in medulloblastoma liquid biopsies
Nearly one-third of children with medulloblastoma, a malignant embryonal tumor of the cerebellum, succumb to their disease. Conventional response monitoring by imaging and cerebrospinal fluid (CSF) cytology remains challenging and a marker for measurable residual disease (MRD) is lacking. Here, we s...
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/PMC9164954/ http://dx.doi.org/10.1093/neuonc/noac079.448 |
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author | Northcott, Paul Smith, Kyle Kumar, Rahul Paul, Leena Bihannic, Laure Lin, Tong Maass, Kendra Pajtler, Kristian Chintagumpala, Murali Su, Jack Bouffet, Eric Fisher, Michael Gururangan, Sridharan Cohn, Richard Hassall, Tim Hansford, Jordan Klimo, Paul Boop, Frederick Stewart, Clinton Harreld, Julie Merchant, Thomas Tatevossian, Ruth Neale, Geoffrey Lear, Matthew Klco, Jeffery Orr, Brent Ellison, David Gilbertson, Richard Onar-Thomas, Arzu Gajjar, Amar Robinson, Giles |
author_facet | Northcott, Paul Smith, Kyle Kumar, Rahul Paul, Leena Bihannic, Laure Lin, Tong Maass, Kendra Pajtler, Kristian Chintagumpala, Murali Su, Jack Bouffet, Eric Fisher, Michael Gururangan, Sridharan Cohn, Richard Hassall, Tim Hansford, Jordan Klimo, Paul Boop, Frederick Stewart, Clinton Harreld, Julie Merchant, Thomas Tatevossian, Ruth Neale, Geoffrey Lear, Matthew Klco, Jeffery Orr, Brent Ellison, David Gilbertson, Richard Onar-Thomas, Arzu Gajjar, Amar Robinson, Giles |
author_sort | Northcott, Paul |
collection | PubMed |
description | Nearly one-third of children with medulloblastoma, a malignant embryonal tumor of the cerebellum, succumb to their disease. Conventional response monitoring by imaging and cerebrospinal fluid (CSF) cytology remains challenging and a marker for measurable residual disease (MRD) is lacking. Here, we show the clinical utility of CSF-derived cell-free DNA (cfDNA) as a biomarker of MRD in serial samples collected from children with medulloblastoma (123 patients, 476 samples) enrolled on a prospective trial. Using low-coverage whole-genome sequencing, tumor-associated copy-number variations (CNVs) in CSF-derived cfDNA are investigated as an MRD surrogate. MRD is detected at baseline in 85% and 54% of patients with metastatic and localized disease, respectively. The number of MRD-positive patients decline with therapy, yet those with persistent MRD have significantly higher risk of progression. Importantly, MRD detection precedes radiographic progression in half who relapse. Our findings advocate for the prospective assessment of CSF-derived liquid biopsies in future trials for medulloblastoma. |
format | Online Article Text |
id | pubmed-9164954 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-91649542022-06-05 MEDB-74. Serial assessment of measurable residual disease in medulloblastoma liquid biopsies Northcott, Paul Smith, Kyle Kumar, Rahul Paul, Leena Bihannic, Laure Lin, Tong Maass, Kendra Pajtler, Kristian Chintagumpala, Murali Su, Jack Bouffet, Eric Fisher, Michael Gururangan, Sridharan Cohn, Richard Hassall, Tim Hansford, Jordan Klimo, Paul Boop, Frederick Stewart, Clinton Harreld, Julie Merchant, Thomas Tatevossian, Ruth Neale, Geoffrey Lear, Matthew Klco, Jeffery Orr, Brent Ellison, David Gilbertson, Richard Onar-Thomas, Arzu Gajjar, Amar Robinson, Giles Neuro Oncol Medulloblastoma Nearly one-third of children with medulloblastoma, a malignant embryonal tumor of the cerebellum, succumb to their disease. Conventional response monitoring by imaging and cerebrospinal fluid (CSF) cytology remains challenging and a marker for measurable residual disease (MRD) is lacking. Here, we show the clinical utility of CSF-derived cell-free DNA (cfDNA) as a biomarker of MRD in serial samples collected from children with medulloblastoma (123 patients, 476 samples) enrolled on a prospective trial. Using low-coverage whole-genome sequencing, tumor-associated copy-number variations (CNVs) in CSF-derived cfDNA are investigated as an MRD surrogate. MRD is detected at baseline in 85% and 54% of patients with metastatic and localized disease, respectively. The number of MRD-positive patients decline with therapy, yet those with persistent MRD have significantly higher risk of progression. Importantly, MRD detection precedes radiographic progression in half who relapse. Our findings advocate for the prospective assessment of CSF-derived liquid biopsies in future trials for medulloblastoma. Oxford University Press 2022-06-03 /pmc/articles/PMC9164954/ http://dx.doi.org/10.1093/neuonc/noac079.448 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 | Medulloblastoma Northcott, Paul Smith, Kyle Kumar, Rahul Paul, Leena Bihannic, Laure Lin, Tong Maass, Kendra Pajtler, Kristian Chintagumpala, Murali Su, Jack Bouffet, Eric Fisher, Michael Gururangan, Sridharan Cohn, Richard Hassall, Tim Hansford, Jordan Klimo, Paul Boop, Frederick Stewart, Clinton Harreld, Julie Merchant, Thomas Tatevossian, Ruth Neale, Geoffrey Lear, Matthew Klco, Jeffery Orr, Brent Ellison, David Gilbertson, Richard Onar-Thomas, Arzu Gajjar, Amar Robinson, Giles MEDB-74. Serial assessment of measurable residual disease in medulloblastoma liquid biopsies |
title | MEDB-74. Serial assessment of measurable residual disease in medulloblastoma liquid biopsies |
title_full | MEDB-74. Serial assessment of measurable residual disease in medulloblastoma liquid biopsies |
title_fullStr | MEDB-74. Serial assessment of measurable residual disease in medulloblastoma liquid biopsies |
title_full_unstemmed | MEDB-74. Serial assessment of measurable residual disease in medulloblastoma liquid biopsies |
title_short | MEDB-74. Serial assessment of measurable residual disease in medulloblastoma liquid biopsies |
title_sort | medb-74. serial assessment of measurable residual disease in medulloblastoma liquid biopsies |
topic | Medulloblastoma |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9164954/ http://dx.doi.org/10.1093/neuonc/noac079.448 |
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