Lauren R Schaff, Mina Lobbous, Dean Carlow, Ryan Schofield, Igor T Gavrilovic, Alexandra M Miller, Jacqueline B Stone, Anna F Piotrowski, Ugur Sener, Anna Skakodub, Edward P Acosta, Kevin J Ryan, Ingo K Mellinghoff, Lisa M DeAngelis, Louis B Nabors, Christian Grommes
Journal: BMC cancer 2022;22(1):60
PMID: 35027038
BACKGROUND
High-dose methotrexate (HD-MTX) has broad use in the treatment of central nervous system (CNS) malignancies but confers significant toxicity without inpatient hydration and monitoring. Glucarpidase is a bacterial recombinant enzyme dosed at 50 units (u)/kg, resulting in rapid systemic MTX clearance. The aim of this study was to demonstrate feasibility of low-dose glucarpidase to facilitate MTX clearance in patients with CNS lymphoma (CNSL).
METHODS
Eight CNSL patients received HD-MTX 3 or 6 g/m and glucarpidase 2000 or 1000u 24 h later. Treatments repeated every 2 weeks up to 8 cycles.
RESULTS
Fifty-five treatments were administered. Glucarpidase 2000u yielded > 95% reduction in plasma MTX within 15 min following 33/34 doses (97.1%) and glucarpidase 1000u yielded > 95% reduction following 15/20 doses (75%). Anti-glucarpidase antibodies developed in 4 patients and were associated with MTX rebound. In CSF, glucarpidase was not detected and MTX levels remained cytotoxic after 1 (3299.5 nmol/L, n = 8) and 6 h (1254.7 nmol/L, n = 7). Treatment was safe and well-tolerated. Radiographic responses in 6 of 8 patients (75%) were as expected following MTX-based therapy.
CONCLUSIONS
This study demonstrates feasibility of planned-use low-dose glucarpidase for MTX clearance and supports the hypothesis that glucarpidase does not impact MTX efficacy in the CNS.
CLINICAL TRIAL REGISTRATION
NCT03684980 (Registration date 26/09/2018).
© 2022. The Author(s).
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