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Use of Glucarpidase for Methotrexate-Induced Nephrotoxicity During the Treatment of Primary Central Nervous System Lymphoma.

Cureus 2026 Vol.18(1) p. e100718

Fujiwara Y, Takaono A, Kitagawa A, Okamoto M

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High-dose methotrexate (HD-MTX)-based combination chemotherapy remains the mainstay of treatment for primary central nervous system lymphoma (PCNSL).

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APA Fujiwara Y, Takaono A, et al. (2026). Use of Glucarpidase for Methotrexate-Induced Nephrotoxicity During the Treatment of Primary Central Nervous System Lymphoma.. Cureus, 18(1), e100718. https://doi.org/10.7759/cureus.100718
MLA Fujiwara Y, et al.. "Use of Glucarpidase for Methotrexate-Induced Nephrotoxicity During the Treatment of Primary Central Nervous System Lymphoma.." Cureus, vol. 18, no. 1, 2026, pp. e100718.
PMID 41640893

Abstract

High-dose methotrexate (HD-MTX)-based combination chemotherapy remains the mainstay of treatment for primary central nervous system lymphoma (PCNSL). However, MTX-induced nephrotoxicity can occur even with adequate preventive and supportive measures. We report a case of MTX-induced acute kidney injury (AKI) that developed during treatment for PCNSL. During the second course of chemotherapy, serum creatinine increased from 0.74 mg/dL at baseline to 2.15 mg/dL on day 3, accompanied by a peak plasma MTX concentration of 3.89 μmol/L. Following administration of glucarpidase, plasma MTX levels declined to 0.08 μmol/L by day 12, and renal function subsequently improved, with serum creatinine decreasing to 1.47 mg/dL by day 19. This biochemical improvement allowed continuation of MTX-based chemotherapy, and the patient ultimately achieved complete remission after seven courses of treatment. This case highlights the role of glucarpidase in facilitating treatment continuity in the setting of MTX-induced nephrotoxicity and underscores the importance of prompt and appropriate supportive care in the management of PCNSL.

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