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J Pediatr Hematol Oncol ; 43(2): e296-e300, 2021 03 01.
Article in English | MEDLINE | ID: mdl-32398599

ABSTRACT

Imatinib, a tyrosine kinase inhibitor has improved survival in pediatric patients with Philadelphia chromosome-positive B-cell acute lymphoblastic leukemia. There are no formal drug interactions listed between methotrexate and tyrosine kinase inhibitors. Four pediatric patients with Philadelphia chromosome-positive B-cell acute lymphoblastic leukemia had delayed methotrexate clearance during their first cycle of high-dose methotrexate while receiving imatinib, resulting in acute kidney injury. For subsequent high-dose methotrexate cycles, imatinib was withheld resulting in decreased acute kidney injury, shorter time to methotrexate clearance, less toxicity, and shorter hospitalizations. For pediatric patients with acute lymphoblastic leukemia receiving imatinib, we recommend escalated supportive care measures including increased hyperhydration and leucovoruin frequency. For patients with toxicities secondary to delayed clearance or need for glucarpidase, we recommend holding imatinib with subsequent high-dose methotrexate courses.


Subject(s)
Acute Kidney Injury/pathology , Antineoplastic Combined Chemotherapy Protocols/adverse effects , Leukemia, B-Cell/drug therapy , Philadelphia Chromosome , Precursor Cell Lymphoblastic Leukemia-Lymphoma/drug therapy , Acute Kidney Injury/chemically induced , Acute Kidney Injury/metabolism , Adolescent , Adult , Antineoplastic Combined Chemotherapy Protocols/metabolism , Child , Child, Preschool , Female , Follow-Up Studies , Humans , Imatinib Mesylate/administration & dosage , Leukemia, B-Cell/genetics , Leukemia, B-Cell/pathology , Male , Methotrexate/administration & dosage , Precursor Cell Lymphoblastic Leukemia-Lymphoma/genetics , Precursor Cell Lymphoblastic Leukemia-Lymphoma/pathology , Prognosis , Young Adult
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