Age- and Intravenous Methotrexate-Associated Leukoencephalopathy and Its Neurological Impact in Pediatric Patients with Lymphoblastic Leukemia

Methotrexate (MTX) is associated with leukoencephalopathy (LE) in children treated for lymphoblastic leukemia/lymphoma (ALL/LBL). However, large-scale studies with systematic MR acquisition and quantitative volumetric lesion information remain limited. Hence, the prevalence of lesion burdens and the...

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Main Authors: Ilona Rijmenams, Daan Moechars, Anne Uyttebroeck, Ahmed Radwan, Jeroen Blommaert, Sabine Deprez, Stefan Sunaert, Heidi Segers, Céline R. Gillebert, Jurgen Lemiere, Charlotte Sleurs
Format: Article
Language:English
Published: MDPI AG 2021-04-01
Series:Cancers
Subjects:
Online Access:https://www.mdpi.com/2072-6694/13/8/1939
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spelling doaj-79b4ebb3933f4f81b0d1cd7088d510192021-04-16T23:06:41ZengMDPI AGCancers2072-66942021-04-01131939193910.3390/cancers13081939Age- and Intravenous Methotrexate-Associated Leukoencephalopathy and Its Neurological Impact in Pediatric Patients with Lymphoblastic LeukemiaIlona Rijmenams0Daan Moechars1Anne Uyttebroeck2Ahmed Radwan3Jeroen Blommaert4Sabine Deprez5Stefan Sunaert6Heidi Segers7Céline R. Gillebert8Jurgen Lemiere9Charlotte Sleurs10Department of Brain and Cognition, KU Leuven, 3000 Leuven, BelgiumDepartment of Brain and Cognition, KU Leuven, 3000 Leuven, BelgiumDepartment of Pediatric Oncology, KU Leuven, 3000 Leuven, BelgiumLeuven Cancer Institute, KU Leuven, 3000 Leuven, BelgiumLeuven Cancer Institute, KU Leuven, 3000 Leuven, BelgiumLeuven Cancer Institute, KU Leuven, 3000 Leuven, BelgiumLeuven Cancer Institute, KU Leuven, 3000 Leuven, BelgiumDepartment of Pediatric Oncology, KU Leuven, 3000 Leuven, BelgiumDepartment of Brain and Cognition, KU Leuven, 3000 Leuven, BelgiumDepartment of Pediatric Hemato-Oncology, University Hospital Leuven, 3000 Leuven, BelgiumDepartment of Pediatric Oncology, KU Leuven, 3000 Leuven, BelgiumMethotrexate (MTX) is associated with leukoencephalopathy (LE) in children treated for lymphoblastic leukemia/lymphoma (ALL/LBL). However, large-scale studies with systematic MR acquisition and quantitative volumetric lesion information remain limited. Hence, the prevalence of lesion burdens and the potential risk factors of LE in this population are still inconclusive. FLAIR-MRI scans were acquired at the end of treatment in children who were treated for ALL/LBL, which were quantitatively analyzed for LE. Voxels were assigned to the lesion segmentation if indicated by two raters. Logistic and linear regression models were used to test whether lesion presence and size were predicted by risk factors such as age at diagnosis, gender, intrathecal (IT-) or intravenous (IV-)MTX dose, CNS invasion, and acute neurological events. Patients with a pre-existing neurological condition or low-quality MR scan were excluded from the analyses. Of the 129 patients, ten (8%) suffered from CNS invasion. Chemotherapy-associated neurological events were observed in 13 patients (10%) during therapy, and 68 patients (53%) showed LE post-treatment. LE was more frequent in cases of lower age and higher cumulative IV-MTX doses, while the extent of LE and neurological symptoms were associated only with IV-MTX doses. Neurological events were not significantly associated with LE, even though symptomatic patients demonstrated a higher ratio of LE (<i>n</i> = 9/13) than asymptomatic patients (<i>n</i> = 59/116). This study suggests leukoencephalopathy frequently occurs in both symptomatic and asymptomatic leukemia patients. Younger children and patients treated with higher cumulative IV-MTX doses might need more regular screening for early detection and follow-up of associated sequelae.https://www.mdpi.com/2072-6694/13/8/1939childhood hematologychemotherapyneurotoxicityleukoencephalopathyrisk classification
collection DOAJ
language English
format Article
sources DOAJ
author Ilona Rijmenams
Daan Moechars
Anne Uyttebroeck
Ahmed Radwan
Jeroen Blommaert
Sabine Deprez
Stefan Sunaert
Heidi Segers
Céline R. Gillebert
Jurgen Lemiere
Charlotte Sleurs
spellingShingle Ilona Rijmenams
Daan Moechars
Anne Uyttebroeck
Ahmed Radwan
Jeroen Blommaert
Sabine Deprez
Stefan Sunaert
Heidi Segers
Céline R. Gillebert
Jurgen Lemiere
Charlotte Sleurs
Age- and Intravenous Methotrexate-Associated Leukoencephalopathy and Its Neurological Impact in Pediatric Patients with Lymphoblastic Leukemia
Cancers
childhood hematology
chemotherapy
neurotoxicity
leukoencephalopathy
risk classification
author_facet Ilona Rijmenams
Daan Moechars
Anne Uyttebroeck
Ahmed Radwan
Jeroen Blommaert
Sabine Deprez
Stefan Sunaert
Heidi Segers
Céline R. Gillebert
Jurgen Lemiere
Charlotte Sleurs
author_sort Ilona Rijmenams
title Age- and Intravenous Methotrexate-Associated Leukoencephalopathy and Its Neurological Impact in Pediatric Patients with Lymphoblastic Leukemia
title_short Age- and Intravenous Methotrexate-Associated Leukoencephalopathy and Its Neurological Impact in Pediatric Patients with Lymphoblastic Leukemia
title_full Age- and Intravenous Methotrexate-Associated Leukoencephalopathy and Its Neurological Impact in Pediatric Patients with Lymphoblastic Leukemia
title_fullStr Age- and Intravenous Methotrexate-Associated Leukoencephalopathy and Its Neurological Impact in Pediatric Patients with Lymphoblastic Leukemia
title_full_unstemmed Age- and Intravenous Methotrexate-Associated Leukoencephalopathy and Its Neurological Impact in Pediatric Patients with Lymphoblastic Leukemia
title_sort age- and intravenous methotrexate-associated leukoencephalopathy and its neurological impact in pediatric patients with lymphoblastic leukemia
publisher MDPI AG
series Cancers
issn 2072-6694
publishDate 2021-04-01
description Methotrexate (MTX) is associated with leukoencephalopathy (LE) in children treated for lymphoblastic leukemia/lymphoma (ALL/LBL). However, large-scale studies with systematic MR acquisition and quantitative volumetric lesion information remain limited. Hence, the prevalence of lesion burdens and the potential risk factors of LE in this population are still inconclusive. FLAIR-MRI scans were acquired at the end of treatment in children who were treated for ALL/LBL, which were quantitatively analyzed for LE. Voxels were assigned to the lesion segmentation if indicated by two raters. Logistic and linear regression models were used to test whether lesion presence and size were predicted by risk factors such as age at diagnosis, gender, intrathecal (IT-) or intravenous (IV-)MTX dose, CNS invasion, and acute neurological events. Patients with a pre-existing neurological condition or low-quality MR scan were excluded from the analyses. Of the 129 patients, ten (8%) suffered from CNS invasion. Chemotherapy-associated neurological events were observed in 13 patients (10%) during therapy, and 68 patients (53%) showed LE post-treatment. LE was more frequent in cases of lower age and higher cumulative IV-MTX doses, while the extent of LE and neurological symptoms were associated only with IV-MTX doses. Neurological events were not significantly associated with LE, even though symptomatic patients demonstrated a higher ratio of LE (<i>n</i> = 9/13) than asymptomatic patients (<i>n</i> = 59/116). This study suggests leukoencephalopathy frequently occurs in both symptomatic and asymptomatic leukemia patients. Younger children and patients treated with higher cumulative IV-MTX doses might need more regular screening for early detection and follow-up of associated sequelae.
topic childhood hematology
chemotherapy
neurotoxicity
leukoencephalopathy
risk classification
url https://www.mdpi.com/2072-6694/13/8/1939
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