Fixed-dose glucarpidase use for high-dose methotrexate toxicity: A case series in Acute Lymphoblastic Leukemia

Introduction Glucarpidase 50 units per kilogram (units/kg) intravenously is indicated for high-dose methotrexate (HDMTX) toxicity, however lower doses are often used. Case series Three patients with Acute Lymphoblastic Leukemia were administered HDMTX 5g/m 2 intravenously over 24 h, developed toxicity, and required glucarpidase. Retrospective data collection included methotrexate (MTX) and creatinine levels and toxicity management. An acute kidney injury developed for all patients with serum creatinine increasing from 79 micromol/L to 172 micromol/L for patient A, 76 micromol/L to 130 micromol/L for patient B, and 67 micromol/L to 117 micromol/L for patient C. Forty-two hour MTX levels returned as 11, 13, 8.6 micromol/L (target is <1 micromol/L) and serum creatinine peaked at 250, 164, and 125 micromol/L for patients A, B, and C, respectively. Management and outcome Calcium folinate, fluids, sodium bicarbonate, and diuretics were administered as indicated. All patients received glucarpidase 2000 units within 56 h of HDMTX commencing. MTX levels took an average of 12 days to fall to <0.1 micromol/L. Regain of normal renal function post-glucarpidase took 25 and 8 days for patients A and C respectively; patient B was lost to follow up. Discussion With evidence of efficacious glucarpidase dosing lower than 50 units/kg, including in this case series (2000 units), combined with its pharmacokinetic properties, 1000 units should be considered for adult patients less than 200 kilograms with a supratherapeutic MTX level of 200 micromol/L or less, from 24 h or 36 h (depending on the protocol used) to 60 h post-HDMTX commencement. This necessitates one 1000 units vial, reducing cost and potentially improving access.

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Journal
Journal of Oncology Pharmacy Practice
Published
2026-10-07
DOI
https://doi.org/10.1177/10781552261492219
Primary Topic
Acute Lymphoblastic Leukemia research
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article
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article

Fixed-dose glucarpidase use for high-dose methotrexate toxicity: A case series in Acute Lymphoblastic Leukemia

Fiona Swain, Marissa Ryan, Centaine L. Snoswell, Michael Whordley et al.
Journal of Oncology Pharmacy Practice
Acute Lymphoblastic Leukemia research
article

Fixed-dose glucarpidase use for high-dose methotrexate toxicity: A case series in Acute Lymphoblastic Leukemia

Fiona Swain, Marissa Ryan, Centaine L. Snoswell, Michael Whordley, Gail Rowan, Christopher Morris
article en

Abstract

Introduction Glucarpidase 50 units per kilogram (units/kg) intravenously is indicated for high-dose methotrexate (HDMTX) toxicity, however lower doses are often used. Case series Three patients with Acute Lymphoblastic Leukemia were administered HDMTX 5g/m 2 intravenously over 24 h, developed toxicity, and required glucarpidase. Retrospective data collection included methotrexate (MTX) and creatinine levels and toxicity management. An acute kidney injury developed for all patients with serum creatinine increasing from 79 micromol/L to 172 micromol/L for patient A, 76 micromol/L to 130 micromol/L for patient B, and 67 micromol/L to 117 micromol/L for patient C. Forty-two hour MTX levels returned as 11, 13, 8.6 micromol/L (target is <1 micromol/L) and serum creatinine peaked at 250, 164, and 125 micromol/L for patients A, B, and C, respectively. Management and outcome Calcium folinate, fluids, sodium bicarbonate, and diuretics were administered as indicated. All patients received glucarpidase 2000 units within 56 h of HDMTX commencing. MTX levels took an average of 12 days to fall to <0.1 micromol/L. Regain of normal renal function post-glucarpidase took 25 and 8 days for patients A and C respectively; patient B was lost to follow up. Discussion With evidence of efficacious glucarpidase dosing lower than 50 units/kg, including in this case series (2000 units), combined with its pharmacokinetic properties, 1000 units should be considered for adult patients less than 200 kilograms with a supratherapeutic MTX level of 200 micromol/L or less, from 24 h or 36 h (depending on the protocol used) to 60 h post-HDMTX commencement. This necessitates one 1000 units vial, reducing cost and potentially improving access.

Journal of Oncology Pharmacy Practice
Translational Research Institute (AU), The University of Queensland (AU), Peter MacCallum Cancer Centre (AU), Princess Alexandra Hospital (AU)
Openalex Percentile: Top 9%
Acute Lymphoblastic Leukemia research
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