Cargando…
Mortality in Children with Optic Pathway Glioma Treated with Up-Front BB-SFOP Chemotherapy
BACKGROUND: In terms of overall survival (OS), limited data are available for the very long-term outcomes of children treated for optic pathway glioma (OPG) with up-front chemotherapy. Therefore, we undertook this study with the aim of clarifying long-term OS and causes of death in these patients. M...
Autores principales: | , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2015
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4476571/ https://www.ncbi.nlm.nih.gov/pubmed/26098902 http://dx.doi.org/10.1371/journal.pone.0127676 |
_version_ | 1782377613389463552 |
---|---|
author | Rakotonjanahary, Josué De Carli, Emilie Delion, Matthieu Kalifa, Chantal Grill, Jacques Doz, François Leblond, Pierre Bertozzi, Anne-Isabelle Rialland, Xavier |
author_facet | Rakotonjanahary, Josué De Carli, Emilie Delion, Matthieu Kalifa, Chantal Grill, Jacques Doz, François Leblond, Pierre Bertozzi, Anne-Isabelle Rialland, Xavier |
author_sort | Rakotonjanahary, Josué |
collection | PubMed |
description | BACKGROUND: In terms of overall survival (OS), limited data are available for the very long-term outcomes of children treated for optic pathway glioma (OPG) with up-front chemotherapy. Therefore, we undertook this study with the aim of clarifying long-term OS and causes of death in these patients. METHODS: We initiated and analyzed a historical cohort study of 180 children with OPG treated in France with BB-SFOP chemotherapy between 1990 and 2004. The survival distributions were estimated using Kaplan-Meier method. The effect of potential risk factors on the risk of death was described using Cox regression analysis. RESULTS: The OS was 95% [95% CI: 90.6-97.3] 5 years after diagnosis and significantly decreased over time without ever stabilizing: 91.6% at 10 years [95% CI: 86.5-94.8], 80.7% at 15 years [95% CI: 72.7-86.8] and 75.5% [95% CI: 65.6-83] at 18 years. Tumor progression was the most common cause of death (65%). Age and intracranial hypertension at diagnosis were significantly associated with a worse prognosis. Risk of death was increased by 3.1[95% CI: 1.5-6.2] (p=0.002) for patients less than 1 year old at diagnosis and by 5.2[95% CI: 1.5-17.6] (p=0.007) for patients with initial intracranial hypertension. Boys without diencephalic syndrome had a better prognosis (HR: 0.3 [95% CI: 0.1-0.8], p=0.007). CONCLUSIONS: This study shows that i) in children with OPG, OS is not as favorable as previously described and ii) patients can be classified into 2 groups depending on risk factors (age, intracranial hypertension, sex and diencephalic syndrome) with an OS rate of 50.4% at 18 years [95% CI: 31.4-66.6] in children with the worst prognosis. These findings could justify, depending on the initial risk, a different therapeutic approach to this tumor with more aggressive treatment (especially chemotherapy) in patients with high risk factors. |
format | Online Article Text |
id | pubmed-4476571 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-44765712015-06-25 Mortality in Children with Optic Pathway Glioma Treated with Up-Front BB-SFOP Chemotherapy Rakotonjanahary, Josué De Carli, Emilie Delion, Matthieu Kalifa, Chantal Grill, Jacques Doz, François Leblond, Pierre Bertozzi, Anne-Isabelle Rialland, Xavier PLoS One Research Article BACKGROUND: In terms of overall survival (OS), limited data are available for the very long-term outcomes of children treated for optic pathway glioma (OPG) with up-front chemotherapy. Therefore, we undertook this study with the aim of clarifying long-term OS and causes of death in these patients. METHODS: We initiated and analyzed a historical cohort study of 180 children with OPG treated in France with BB-SFOP chemotherapy between 1990 and 2004. The survival distributions were estimated using Kaplan-Meier method. The effect of potential risk factors on the risk of death was described using Cox regression analysis. RESULTS: The OS was 95% [95% CI: 90.6-97.3] 5 years after diagnosis and significantly decreased over time without ever stabilizing: 91.6% at 10 years [95% CI: 86.5-94.8], 80.7% at 15 years [95% CI: 72.7-86.8] and 75.5% [95% CI: 65.6-83] at 18 years. Tumor progression was the most common cause of death (65%). Age and intracranial hypertension at diagnosis were significantly associated with a worse prognosis. Risk of death was increased by 3.1[95% CI: 1.5-6.2] (p=0.002) for patients less than 1 year old at diagnosis and by 5.2[95% CI: 1.5-17.6] (p=0.007) for patients with initial intracranial hypertension. Boys without diencephalic syndrome had a better prognosis (HR: 0.3 [95% CI: 0.1-0.8], p=0.007). CONCLUSIONS: This study shows that i) in children with OPG, OS is not as favorable as previously described and ii) patients can be classified into 2 groups depending on risk factors (age, intracranial hypertension, sex and diencephalic syndrome) with an OS rate of 50.4% at 18 years [95% CI: 31.4-66.6] in children with the worst prognosis. These findings could justify, depending on the initial risk, a different therapeutic approach to this tumor with more aggressive treatment (especially chemotherapy) in patients with high risk factors. Public Library of Science 2015-06-22 /pmc/articles/PMC4476571/ /pubmed/26098902 http://dx.doi.org/10.1371/journal.pone.0127676 Text en © 2015 Rakotonjanahary et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Rakotonjanahary, Josué De Carli, Emilie Delion, Matthieu Kalifa, Chantal Grill, Jacques Doz, François Leblond, Pierre Bertozzi, Anne-Isabelle Rialland, Xavier Mortality in Children with Optic Pathway Glioma Treated with Up-Front BB-SFOP Chemotherapy |
title | Mortality in Children with Optic Pathway Glioma Treated with Up-Front BB-SFOP Chemotherapy |
title_full | Mortality in Children with Optic Pathway Glioma Treated with Up-Front BB-SFOP Chemotherapy |
title_fullStr | Mortality in Children with Optic Pathway Glioma Treated with Up-Front BB-SFOP Chemotherapy |
title_full_unstemmed | Mortality in Children with Optic Pathway Glioma Treated with Up-Front BB-SFOP Chemotherapy |
title_short | Mortality in Children with Optic Pathway Glioma Treated with Up-Front BB-SFOP Chemotherapy |
title_sort | mortality in children with optic pathway glioma treated with up-front bb-sfop chemotherapy |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4476571/ https://www.ncbi.nlm.nih.gov/pubmed/26098902 http://dx.doi.org/10.1371/journal.pone.0127676 |
work_keys_str_mv | AT rakotonjanaharyjosue mortalityinchildrenwithopticpathwaygliomatreatedwithupfrontbbsfopchemotherapy AT decarliemilie mortalityinchildrenwithopticpathwaygliomatreatedwithupfrontbbsfopchemotherapy AT delionmatthieu mortalityinchildrenwithopticpathwaygliomatreatedwithupfrontbbsfopchemotherapy AT kalifachantal mortalityinchildrenwithopticpathwaygliomatreatedwithupfrontbbsfopchemotherapy AT grilljacques mortalityinchildrenwithopticpathwaygliomatreatedwithupfrontbbsfopchemotherapy AT dozfrancois mortalityinchildrenwithopticpathwaygliomatreatedwithupfrontbbsfopchemotherapy AT leblondpierre mortalityinchildrenwithopticpathwaygliomatreatedwithupfrontbbsfopchemotherapy AT bertozzianneisabelle mortalityinchildrenwithopticpathwaygliomatreatedwithupfrontbbsfopchemotherapy AT riallandxavier mortalityinchildrenwithopticpathwaygliomatreatedwithupfrontbbsfopchemotherapy AT mortalityinchildrenwithopticpathwaygliomatreatedwithupfrontbbsfopchemotherapy |