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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2022
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.
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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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