Prevention and Treatment of Acute Kidney Injury Associated with High-Dose Methotrexate.

IF 3 Q1 UROLOGY & NEPHROLOGY Kidney360 Pub Date : 2025-03-01 Epub Date: 2025-01-31 DOI:10.34067/KID.0000000725
Stanislas Faguer, Chloé Medrano, Suzanne Tavitian, Lucie Oberic
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Abstract

AKI is a rare but life-threatening complication of the administration of methotrexate (MTX) at high doses (≥1 g/m 2 ) for the treatment of solid or hematological malignancies. MTX overexposure can lead to MTX-AKI and subsequent higher risk of extrakidney toxicities, morbidity, and mortality. MTX-AKI can also lead to secondary CKD requiring a reduced dose or contraindication for subsequent MTX infusions, thus worsening the cancer-related prognosis. Treatment of MTX-AKI is mainly preventive, combining alkaline hyperhydration, withdrawal of all nephrotoxic agents and drugs that modulate the metabolism of MTX, metabolic salvage using leucovorin (folinic acid), and close monitoring of serum MTX and creatinine concentrations. Glucarpidase (carboxypeptidase-G2), a recombinant bacterial enzyme that hydrolyzes MTX into two noncytotoxic metabolites, should be considered for patients with MTX overexposure to prevent and lessen AKI and other potential toxicities. This article provides a comprehensive review of MTX metabolism, mechanisms and prevention of MTX-AKI, and its management.

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大剂量甲氨蝶呤所致急性肾损伤的防治。
急性肾损伤(AKI)是高剂量(≥1g /m2)甲氨蝶呤(MTX)治疗实体或血液恶性肿瘤时罕见但危及生命的并发症。甲氨蝶呤过度暴露可导致甲氨蝶呤aki,以及随后更高的肾外毒性、发病率和死亡率风险。MTX- aki还可导致继发性慢性肾脏疾病,需要减少剂量或禁止后续MTX输注,从而恶化癌症相关预后。MTX- aki的治疗主要是预防性的,包括碱性多水化,停用所有肾毒性药物和调节MTX代谢的药物,使用亚叶酸进行代谢恢复,密切监测血清MTX和肌酐浓度。葡萄糖苷酶(羧肽酶- g2)是一种重组细菌酶,可将MTX水解成两种无细胞毒性的代谢物,对于MTX过度暴露的患者,应考虑使用葡萄糖苷酶来预防和减轻AKI和其他潜在的毒性。本文就MTX代谢、MTX- aki的机制、预防及其管理等方面进行综述。
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来源期刊
Kidney360
Kidney360 UROLOGY & NEPHROLOGY-
CiteScore
3.90
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0.00%
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