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DIPG-25. Patterns of cerebrospinal fluid diversion and survival in children with diffuse intrinsic pontine glioma: a report from the International Diffuse Intrinsic Pontine Glioma Registry
BACKGROUND: There are no standard practice guidelines for cerebrospinal (CSF) diversion for diffuse intrinsic pontine glioma (DIPG), nor clear understanding of potential for palliation and life-prolongation. We evaluated CSF diversion characteristics in children with DIPG to determine incidence, ind...
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/PMC9164972/ http://dx.doi.org/10.1093/neuonc/noac079.082 |
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author | Cooney, Tabitha DeWire-Schottmiller, Mariko Lane, Adam Saab, Raya Bandopadhayay, Pratiti Dorris, Kathleen Packer, Roger Kilburn, Lindsay Minturn, Jane Dodgshun, Andrew Parkin, Sara Goldman, Stewart Sandler, Eric Greiner, Robert Gottardo, Nicholas Dholaria, Hetal Coven, Scott Hassall, Tim Hansford, Jordan Samson, Yvan Leary, Sarah Bartels, Ute Fonseca, Adriana Bouffet, Eric Tinkle, Christopher Monje, Michelle Fisher, Paul Ziegler, David Chintagumpala, Murali Wagner, Lars Koschmann, Carl Leach, James Jones, Blaise Benito, Elisa Carrasquedo Bond, Hailey Chaney, Brooklyn Black, Katie Asher, Anthony Fouladi, Maryam Hoffman, Lindsey Warren, Katherine |
author_facet | Cooney, Tabitha DeWire-Schottmiller, Mariko Lane, Adam Saab, Raya Bandopadhayay, Pratiti Dorris, Kathleen Packer, Roger Kilburn, Lindsay Minturn, Jane Dodgshun, Andrew Parkin, Sara Goldman, Stewart Sandler, Eric Greiner, Robert Gottardo, Nicholas Dholaria, Hetal Coven, Scott Hassall, Tim Hansford, Jordan Samson, Yvan Leary, Sarah Bartels, Ute Fonseca, Adriana Bouffet, Eric Tinkle, Christopher Monje, Michelle Fisher, Paul Ziegler, David Chintagumpala, Murali Wagner, Lars Koschmann, Carl Leach, James Jones, Blaise Benito, Elisa Carrasquedo Bond, Hailey Chaney, Brooklyn Black, Katie Asher, Anthony Fouladi, Maryam Hoffman, Lindsey Warren, Katherine |
author_sort | Cooney, Tabitha |
collection | PubMed |
description | BACKGROUND: There are no standard practice guidelines for cerebrospinal (CSF) diversion for diffuse intrinsic pontine glioma (DIPG), nor clear understanding of potential for palliation and life-prolongation. We evaluated CSF diversion characteristics in children with DIPG to determine incidence, indications, symptom effects, and survival. METHODS: Data were extracted from subjects registered in the International DIPG registry (IDIPGR). Univariable analyses was performed using the Fisher’s exact test or Wilcoxon rank sum test. Survival was estimated using the Kaplan-Meier method. RESULTS: Evaluable patients (n=542) met criteria for DIPG diagnosis by central radiologic review; of those, 126 (23%) had permanent CSF diversion. Median time from diagnosis to diversion was 0.5 months (IQR 0.1-4.5 months). Those with permanent diversion were significantly younger (median 5.4 years vs 7.0 years, p<0.001) and had higher incidence of hydrocephalus at diagnosis (65.3% vs 11.9%, p<0.001). Permanent CSF diversion did not significantly impact overall survival (OS) (p=0.4), even amongst the 124 patients with hydrocephalus at presentation (p=0.20). Those with permanent diversion prior to radiation therapy demonstrated longer median OS than those in whom diversion was placed after radiation (14.3 vs 9.6 months, p=0.001). Patients reported significantly less headache and vomiting at last follow up after permanent CSF diversion compared to pre-diversion (p<0.0001 and p=0.001, respectively), however steroid use was also significantly higher at last follow-up after CSF diversion (p<0.001). CONCLUSIONS: Amongst an international cohort, DIPG patients who had permanent CSF diversion were significantly younger and had higher rates of hydrocephalus at initial presentation than those without permanent diversion. Symptoms of increased intracranial pressure improved in those with CSF diversion, although a direct effect may be confounded by increased steroid use. Permanent CSF diversion did not prolong overall survival in this large cohort of patients, even amongst those who presented with hydrocephalus. |
format | Online Article Text |
id | pubmed-9164972 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-91649722022-06-05 DIPG-25. Patterns of cerebrospinal fluid diversion and survival in children with diffuse intrinsic pontine glioma: a report from the International Diffuse Intrinsic Pontine Glioma Registry Cooney, Tabitha DeWire-Schottmiller, Mariko Lane, Adam Saab, Raya Bandopadhayay, Pratiti Dorris, Kathleen Packer, Roger Kilburn, Lindsay Minturn, Jane Dodgshun, Andrew Parkin, Sara Goldman, Stewart Sandler, Eric Greiner, Robert Gottardo, Nicholas Dholaria, Hetal Coven, Scott Hassall, Tim Hansford, Jordan Samson, Yvan Leary, Sarah Bartels, Ute Fonseca, Adriana Bouffet, Eric Tinkle, Christopher Monje, Michelle Fisher, Paul Ziegler, David Chintagumpala, Murali Wagner, Lars Koschmann, Carl Leach, James Jones, Blaise Benito, Elisa Carrasquedo Bond, Hailey Chaney, Brooklyn Black, Katie Asher, Anthony Fouladi, Maryam Hoffman, Lindsey Warren, Katherine Neuro Oncol Diffuse Midline Glioma/DIPG BACKGROUND: There are no standard practice guidelines for cerebrospinal (CSF) diversion for diffuse intrinsic pontine glioma (DIPG), nor clear understanding of potential for palliation and life-prolongation. We evaluated CSF diversion characteristics in children with DIPG to determine incidence, indications, symptom effects, and survival. METHODS: Data were extracted from subjects registered in the International DIPG registry (IDIPGR). Univariable analyses was performed using the Fisher’s exact test or Wilcoxon rank sum test. Survival was estimated using the Kaplan-Meier method. RESULTS: Evaluable patients (n=542) met criteria for DIPG diagnosis by central radiologic review; of those, 126 (23%) had permanent CSF diversion. Median time from diagnosis to diversion was 0.5 months (IQR 0.1-4.5 months). Those with permanent diversion were significantly younger (median 5.4 years vs 7.0 years, p<0.001) and had higher incidence of hydrocephalus at diagnosis (65.3% vs 11.9%, p<0.001). Permanent CSF diversion did not significantly impact overall survival (OS) (p=0.4), even amongst the 124 patients with hydrocephalus at presentation (p=0.20). Those with permanent diversion prior to radiation therapy demonstrated longer median OS than those in whom diversion was placed after radiation (14.3 vs 9.6 months, p=0.001). Patients reported significantly less headache and vomiting at last follow up after permanent CSF diversion compared to pre-diversion (p<0.0001 and p=0.001, respectively), however steroid use was also significantly higher at last follow-up after CSF diversion (p<0.001). CONCLUSIONS: Amongst an international cohort, DIPG patients who had permanent CSF diversion were significantly younger and had higher rates of hydrocephalus at initial presentation than those without permanent diversion. Symptoms of increased intracranial pressure improved in those with CSF diversion, although a direct effect may be confounded by increased steroid use. Permanent CSF diversion did not prolong overall survival in this large cohort of patients, even amongst those who presented with hydrocephalus. Oxford University Press 2022-06-03 /pmc/articles/PMC9164972/ http://dx.doi.org/10.1093/neuonc/noac079.082 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 | Diffuse Midline Glioma/DIPG Cooney, Tabitha DeWire-Schottmiller, Mariko Lane, Adam Saab, Raya Bandopadhayay, Pratiti Dorris, Kathleen Packer, Roger Kilburn, Lindsay Minturn, Jane Dodgshun, Andrew Parkin, Sara Goldman, Stewart Sandler, Eric Greiner, Robert Gottardo, Nicholas Dholaria, Hetal Coven, Scott Hassall, Tim Hansford, Jordan Samson, Yvan Leary, Sarah Bartels, Ute Fonseca, Adriana Bouffet, Eric Tinkle, Christopher Monje, Michelle Fisher, Paul Ziegler, David Chintagumpala, Murali Wagner, Lars Koschmann, Carl Leach, James Jones, Blaise Benito, Elisa Carrasquedo Bond, Hailey Chaney, Brooklyn Black, Katie Asher, Anthony Fouladi, Maryam Hoffman, Lindsey Warren, Katherine DIPG-25. Patterns of cerebrospinal fluid diversion and survival in children with diffuse intrinsic pontine glioma: a report from the International Diffuse Intrinsic Pontine Glioma Registry |
title | DIPG-25. Patterns of cerebrospinal fluid diversion and survival in children with diffuse intrinsic pontine glioma: a report from the International Diffuse Intrinsic Pontine Glioma Registry |
title_full | DIPG-25. Patterns of cerebrospinal fluid diversion and survival in children with diffuse intrinsic pontine glioma: a report from the International Diffuse Intrinsic Pontine Glioma Registry |
title_fullStr | DIPG-25. Patterns of cerebrospinal fluid diversion and survival in children with diffuse intrinsic pontine glioma: a report from the International Diffuse Intrinsic Pontine Glioma Registry |
title_full_unstemmed | DIPG-25. Patterns of cerebrospinal fluid diversion and survival in children with diffuse intrinsic pontine glioma: a report from the International Diffuse Intrinsic Pontine Glioma Registry |
title_short | DIPG-25. Patterns of cerebrospinal fluid diversion and survival in children with diffuse intrinsic pontine glioma: a report from the International Diffuse Intrinsic Pontine Glioma Registry |
title_sort | dipg-25. patterns of cerebrospinal fluid diversion and survival in children with diffuse intrinsic pontine glioma: a report from the international diffuse intrinsic pontine glioma registry |
topic | Diffuse Midline Glioma/DIPG |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9164972/ http://dx.doi.org/10.1093/neuonc/noac079.082 |
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