BMC Cancer (Jan 2022)

Routine use of low-dose glucarpidase following high-dose methotrexate in adult patients with CNS lymphoma: an open-label, multi-center phase I study

  • 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

DOI
https://doi.org/10.1186/s12885-021-09164-x
Journal volume & issue
Vol. 22, no. 1
pp. 1 – 10

Abstract

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Abstract 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/m2 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).

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