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用于治疗危及生命的甲氨蝶呤过量的羧肽酶G2。

Glucarpidase for the treatment of life-threatening methotrexate overdose.

作者信息

Tuffaha H W, Al Omar S

机构信息

Department of Pharmacy, King Hussein Cancer Center, Amman, Jordan.

出版信息

Drugs Today (Barc). 2012 Nov;48(11):705-11. doi: 10.1358/dot.2012.48.11.1871575.

Abstract

High-dose methotrexate (HDMTX) is widely and safely used in oncology, with adequate measures including vigorous hydration, urine alkalinization and leucovorin rescue. Despite these precautions, some patients still develop HDMTX-induced nephrotoxicity, which leads to delayed methotrexate (MTX) clearance and sustained elevated plasma MTX levels, which can significantly increase MTX toxicity. Glucarpidase (carboxypeptidase G2, Voraxase®) is a recombinant bacterial enzyme that rapidly hydrolyzes MTX to inactive metabolites, providing an alternate non-renal pathway for MTX elimination in patients with renal dysfunction during HDMTX treatment. Glucarpidase has recently been approved for the treatment of toxic plasma MTX concentrations in patients with delayed MTX clearance due to impaired renal function. Preclinical and clinical studies demonstrated good safety and efficacy in rapidly reducing elevated MTX levels. Further comparative studies are awaited to confirm the benefit of glucarpidase in terms of toxicity and survival.

摘要

大剂量甲氨蝶呤(HDMTX)在肿瘤学领域被广泛且安全地使用,同时采取了包括积极补液、尿液碱化和亚叶酸解救等适当措施。尽管有这些预防措施,但仍有一些患者会发生HDMTX诱导的肾毒性,这会导致甲氨蝶呤(MTX)清除延迟和血浆MTX水平持续升高,进而显著增加MTX毒性。羧肽酶G2(卡泊酸酶,商品名Voraxase®)是一种重组细菌酶,可迅速将MTX水解为无活性的代谢产物,为HDMTX治疗期间肾功能不全患者的MTX消除提供了一条非肾脏的替代途径。卡泊酸酶最近已被批准用于治疗因肾功能受损导致MTX清除延迟的患者的血浆MTX中毒浓度。临床前和临床研究表明,其在迅速降低升高的MTX水平方面具有良好的安全性和有效性。有待进一步的比较研究来证实卡泊酸酶在毒性和生存率方面的益处。

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