Cargando…

LGG-24. Neurocognitive impairment and functional independence in adult survivors of childhood glioma: A report from the Childhood Cancer Survivor Study (CCSS)

PURPOSE: Survivors of pediatric glioma are at risk of developing physical and neurocognitive sequelae secondary to their tumor and its treatment. The contribution of these conditions to attainment of functional independence has not previously been examined. METHODS: 1,284 adult survivors of pediatri...

Descripción completa

Detalles Bibliográficos
Autores principales: Papini, Chiara, Xing, Mengqi, Salehabadi, Sedigheh Mirzaei, Olsson, Ingrid Tonning, Lange, Katharine, de Blank, Peter, Salloum, Ralph, Srivastava, Deo Kumar, Leisenring, Wendy M, Howell, Rebecca M, Oeffinger, Kevin, Robison, Leslie L, Armstrong, Gregory T, Krull, Kevin R, Brinkman, Tara M
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9164926/
http://dx.doi.org/10.1093/neuonc/noac079.338
_version_ 1784720261765922816
author Papini, Chiara
Xing, Mengqi
Salehabadi, Sedigheh Mirzaei
Olsson, Ingrid Tonning
Lange, Katharine
de Blank, Peter
Salloum, Ralph
Srivastava, Deo Kumar
Leisenring, Wendy M
Howell, Rebecca M
Oeffinger, Kevin
Robison, Leslie L
Armstrong, Gregory T
Krull, Kevin R
Brinkman, Tara M
author_facet Papini, Chiara
Xing, Mengqi
Salehabadi, Sedigheh Mirzaei
Olsson, Ingrid Tonning
Lange, Katharine
de Blank, Peter
Salloum, Ralph
Srivastava, Deo Kumar
Leisenring, Wendy M
Howell, Rebecca M
Oeffinger, Kevin
Robison, Leslie L
Armstrong, Gregory T
Krull, Kevin R
Brinkman, Tara M
author_sort Papini, Chiara
collection PubMed
description PURPOSE: Survivors of pediatric glioma are at risk of developing physical and neurocognitive sequelae secondary to their tumor and its treatment. The contribution of these conditions to attainment of functional independence has not previously been examined. METHODS: 1,284 adult survivors of pediatric glioma (48% male, median [range] 30 [18-51] years at assessment, 22 [15-34] years since diagnosis) completed the CCSS Neurocognitive Questionnaire with impairment defined as scores > 90th %ile of sibling norms. Treatment exposures were categorized as surgery only, chemotherapy (± surgery), or cranial radiation (± chemotherapy/surgery). Self-reported chronic health conditions (CHCs) were graded by organ system using NCI’s CTCAE v4.3. Latent class analysis utilized six factors (employment, marital status, independent living, driver’s license, assistance with routine needs, assistance with personal care needs) to identify classes of functional independence. Multivariable modified Poisson regression evaluated relative risk (RR) of neurocognitive impairment between the classes, adjusting for sex, race, age at assessment, and age at diagnosis. Path analysis explored the impact of treatment exposures on functional independence, mediated by Grade 2-4 CHCs and neurocognitive impairment. RESULTS: Three latent classes of functional independence were identified: independent (58%), moderately independent (20%), and non-independent (22%). Compared to the independent class, non-independent survivors were at elevated risk for impaired task efficiency (RR=3.86, 95% CI, 2.97-5.01), memory (RR=2.39, 95% CI, 1.91-2.98), organization (RR=2.04, 95% CI, 1.64-2.54), and emotional regulation (RR=1.67, 95% CI, 1.30-2.15). Path analysis revealed significant direct paths from cranial radiation (β=0.14), impaired task efficiency (β=0.42), and sensorimotor (β=0.22) and endocrine conditions (β=0.24) to non-independence. Cranial radiation also was indirectly associated with non-independence through impaired task efficiency (β=0.06), and sensorimotor (β=0.06) and endocrine conditions (β=0.10). CONCLUSIONS: Neurocognitive impairment and chronic health conditions partially mediate the association between treatment exposures and attainment of independence in adulthood, identifying potential intervention targets to promote independence in long-term survivors.
format Online
Article
Text
id pubmed-9164926
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher Oxford University Press
record_format MEDLINE/PubMed
spelling pubmed-91649262022-06-05 LGG-24. Neurocognitive impairment and functional independence in adult survivors of childhood glioma: A report from the Childhood Cancer Survivor Study (CCSS) Papini, Chiara Xing, Mengqi Salehabadi, Sedigheh Mirzaei Olsson, Ingrid Tonning Lange, Katharine de Blank, Peter Salloum, Ralph Srivastava, Deo Kumar Leisenring, Wendy M Howell, Rebecca M Oeffinger, Kevin Robison, Leslie L Armstrong, Gregory T Krull, Kevin R Brinkman, Tara M Neuro Oncol Low Grade Glioma PURPOSE: Survivors of pediatric glioma are at risk of developing physical and neurocognitive sequelae secondary to their tumor and its treatment. The contribution of these conditions to attainment of functional independence has not previously been examined. METHODS: 1,284 adult survivors of pediatric glioma (48% male, median [range] 30 [18-51] years at assessment, 22 [15-34] years since diagnosis) completed the CCSS Neurocognitive Questionnaire with impairment defined as scores > 90th %ile of sibling norms. Treatment exposures were categorized as surgery only, chemotherapy (± surgery), or cranial radiation (± chemotherapy/surgery). Self-reported chronic health conditions (CHCs) were graded by organ system using NCI’s CTCAE v4.3. Latent class analysis utilized six factors (employment, marital status, independent living, driver’s license, assistance with routine needs, assistance with personal care needs) to identify classes of functional independence. Multivariable modified Poisson regression evaluated relative risk (RR) of neurocognitive impairment between the classes, adjusting for sex, race, age at assessment, and age at diagnosis. Path analysis explored the impact of treatment exposures on functional independence, mediated by Grade 2-4 CHCs and neurocognitive impairment. RESULTS: Three latent classes of functional independence were identified: independent (58%), moderately independent (20%), and non-independent (22%). Compared to the independent class, non-independent survivors were at elevated risk for impaired task efficiency (RR=3.86, 95% CI, 2.97-5.01), memory (RR=2.39, 95% CI, 1.91-2.98), organization (RR=2.04, 95% CI, 1.64-2.54), and emotional regulation (RR=1.67, 95% CI, 1.30-2.15). Path analysis revealed significant direct paths from cranial radiation (β=0.14), impaired task efficiency (β=0.42), and sensorimotor (β=0.22) and endocrine conditions (β=0.24) to non-independence. Cranial radiation also was indirectly associated with non-independence through impaired task efficiency (β=0.06), and sensorimotor (β=0.06) and endocrine conditions (β=0.10). CONCLUSIONS: Neurocognitive impairment and chronic health conditions partially mediate the association between treatment exposures and attainment of independence in adulthood, identifying potential intervention targets to promote independence in long-term survivors. Oxford University Press 2022-06-03 /pmc/articles/PMC9164926/ http://dx.doi.org/10.1093/neuonc/noac079.338 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
Papini, Chiara
Xing, Mengqi
Salehabadi, Sedigheh Mirzaei
Olsson, Ingrid Tonning
Lange, Katharine
de Blank, Peter
Salloum, Ralph
Srivastava, Deo Kumar
Leisenring, Wendy M
Howell, Rebecca M
Oeffinger, Kevin
Robison, Leslie L
Armstrong, Gregory T
Krull, Kevin R
Brinkman, Tara M
LGG-24. Neurocognitive impairment and functional independence in adult survivors of childhood glioma: A report from the Childhood Cancer Survivor Study (CCSS)
title LGG-24. Neurocognitive impairment and functional independence in adult survivors of childhood glioma: A report from the Childhood Cancer Survivor Study (CCSS)
title_full LGG-24. Neurocognitive impairment and functional independence in adult survivors of childhood glioma: A report from the Childhood Cancer Survivor Study (CCSS)
title_fullStr LGG-24. Neurocognitive impairment and functional independence in adult survivors of childhood glioma: A report from the Childhood Cancer Survivor Study (CCSS)
title_full_unstemmed LGG-24. Neurocognitive impairment and functional independence in adult survivors of childhood glioma: A report from the Childhood Cancer Survivor Study (CCSS)
title_short LGG-24. Neurocognitive impairment and functional independence in adult survivors of childhood glioma: A report from the Childhood Cancer Survivor Study (CCSS)
title_sort lgg-24. neurocognitive impairment and functional independence in adult survivors of childhood glioma: a report from the childhood cancer survivor study (ccss)
topic Low Grade Glioma
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9164926/
http://dx.doi.org/10.1093/neuonc/noac079.338
work_keys_str_mv AT papinichiara lgg24neurocognitiveimpairmentandfunctionalindependenceinadultsurvivorsofchildhoodgliomaareportfromthechildhoodcancersurvivorstudyccss
AT xingmengqi lgg24neurocognitiveimpairmentandfunctionalindependenceinadultsurvivorsofchildhoodgliomaareportfromthechildhoodcancersurvivorstudyccss
AT salehabadisedighehmirzaei lgg24neurocognitiveimpairmentandfunctionalindependenceinadultsurvivorsofchildhoodgliomaareportfromthechildhoodcancersurvivorstudyccss
AT olssoningridtonning lgg24neurocognitiveimpairmentandfunctionalindependenceinadultsurvivorsofchildhoodgliomaareportfromthechildhoodcancersurvivorstudyccss
AT langekatharine lgg24neurocognitiveimpairmentandfunctionalindependenceinadultsurvivorsofchildhoodgliomaareportfromthechildhoodcancersurvivorstudyccss
AT deblankpeter lgg24neurocognitiveimpairmentandfunctionalindependenceinadultsurvivorsofchildhoodgliomaareportfromthechildhoodcancersurvivorstudyccss
AT salloumralph lgg24neurocognitiveimpairmentandfunctionalindependenceinadultsurvivorsofchildhoodgliomaareportfromthechildhoodcancersurvivorstudyccss
AT srivastavadeokumar lgg24neurocognitiveimpairmentandfunctionalindependenceinadultsurvivorsofchildhoodgliomaareportfromthechildhoodcancersurvivorstudyccss
AT leisenringwendym lgg24neurocognitiveimpairmentandfunctionalindependenceinadultsurvivorsofchildhoodgliomaareportfromthechildhoodcancersurvivorstudyccss
AT howellrebeccam lgg24neurocognitiveimpairmentandfunctionalindependenceinadultsurvivorsofchildhoodgliomaareportfromthechildhoodcancersurvivorstudyccss
AT oeffingerkevin lgg24neurocognitiveimpairmentandfunctionalindependenceinadultsurvivorsofchildhoodgliomaareportfromthechildhoodcancersurvivorstudyccss
AT robisonlesliel lgg24neurocognitiveimpairmentandfunctionalindependenceinadultsurvivorsofchildhoodgliomaareportfromthechildhoodcancersurvivorstudyccss
AT armstronggregoryt lgg24neurocognitiveimpairmentandfunctionalindependenceinadultsurvivorsofchildhoodgliomaareportfromthechildhoodcancersurvivorstudyccss
AT krullkevinr lgg24neurocognitiveimpairmentandfunctionalindependenceinadultsurvivorsofchildhoodgliomaareportfromthechildhoodcancersurvivorstudyccss
AT brinkmantaram lgg24neurocognitiveimpairmentandfunctionalindependenceinadultsurvivorsofchildhoodgliomaareportfromthechildhoodcancersurvivorstudyccss