Key result
Methotrexate use in pediatric cancer linked to leukoencephalopathy and cognitive decline, driven by age and dose.
Why the study?
Methotrexate is widely used for pediatric acute lymphoblastic leukemia but causes neurotoxic effects such as leukoencephalopathy that can profoundly impact quality of life and neurocognitive development.
What are the clinical and imaging characteristics of methotrexate-related leukoencephalopathy in pediatric cancer patients?
What are the clinical and imaging characteristics of methotrexate-related leukoencephalopathy in pediatric cancer patients?
Methotrexate-induced leukoencephalopathy is a significant clinical challenge in pediatric cancer survivors, with age and cumulative dose being primary determinants of vulnerability.
Raises awareness for neurotoxicity monitoring in MTX-treated pediatric ALL; leaves open need for prospective incidence and prevention data.
Methotrexate (MTX) is widely used in the treatment of acute lymphoblastic leukemia (ALL) in children but is associated with neurotoxic effects, including leukoencephalopathy (LE). These effects can profoundly affect quality of life and neurocognitive development. We conducted a literature review across multiple databases between 2014 and 2024. The study population included children and adolescents with cancer (under 22 years old) treated with MTX, focusing on LE. Case reports, case series, and reviews were excluded. We analyzed factors such as age, dose, and route of administration (intrathecal or intravenous), correlating clinical and imaging data with neurocognitive outcomes. We included 12 of the 262 identified studies. Most studies involved survivors of childhood cancer diagnosed with ALL (n = 11). LE presented heterogeneously, with clinical manifestations such as seizures, focal neurological deficits, and subtle cognitive declines, particularly in working memory and processing speed. A substantial portion of the lesions persisted even after treatment completion, emphasizing the link between white matter microstructural changes and MTX use. Results indicated that the combination of age and cumulative dose acted as the primary determinant of vulnerability. MTX-induced LE is a significant clinical challenge. Early detection and longitudinal monitoring are crucial to minimize neurocognitive impacts in pediatric survivors. Future research should focus on strategies to mitigate neurotoxicity and optimize quality of life for ALL survivors.
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Ribeiro et al. (2026) conducted a review in Pediatric cancer (primarily acute lymphoblastic leukemia) (n=12). Methotrexate was evaluated on Leukoencephalopathy and neurocognitive outcomes. Methotrexate use in pediatric cancer patients is associated with leukoencephalopathy and cognitive declines, with vulnerability primarily determined by age and cumulative dose.
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