Division of Research in Patient Services, Cincinnati Children's Hospital Medical Center, Department of Pediatrics, College of Medicine, University of Cincinnati, Cincinnati, Ohio, USA
Division of Clinical Pharmacology, Cincinnati Children's Hospital Medical Center, Department of Pediatrics, College of Medicine, University of Cincinnati, Cincinnati, Ohio, USA.
Oncologist. 2018 Jan;23(1):52-61. doi: 10.1634/theoncologist.2017-0243. Epub 2017 Oct 27.
Acute kidney injury due to high-dose methotrexate (HDMTX) is a serious, life-threatening toxicity that can occur in pediatric and adult patients. Glucarpidase is a treatment approved by the Food and Drug Administration for high methotrexate concentrations in the context of kidney dysfunction, but the guidelines for when to use it are unclear. An expert panel was convened to provide specific, expert consensus guidelines for the use of glucarpidase in patients who develop HDMTX-induced nephrotoxicity and delayed methotrexate excretion. The guideline provides recommendations to identify the population of patients who would benefit from glucarpidase rescue by more precisely defining the absolute methotrexate concentrations associated with risk for severe or life-threatening toxicity at several time points after the start of an HDMTX infusion. For an HDMTX infusion ≤24 hours, if the 36-hour concentration is above 30 µM, 42-hour concentration is above 10 µM, or 48-hour concentration is above 5 µM and the serum creatinine is significantly elevated relative to the baseline measurement (indicative of HDMTX-induced acute kidney injury), glucarpidase may be indicated. After a 36- to 42-hour HDMTX infusion, glucarpidase may be indicated when the 48-hour methotrexate concentration is above 5 µM. Administration of glucarpidase should optimally occur within 48-60 hours from the start of the HDMTX infusion, because life-threatening toxicities may not be preventable beyond this time point.
Glucarpidase is a rarely used medication that is less effective when given after more than 60 hours of exposure to high-dose methotrexate, so predicting early which patients will need it is imperative. There are no currently available consensus guidelines for the use of this medication. The indication on the label does not give specific methotrexate concentrations above which it should be used. An international group of experts was convened to develop a consensus guideline that was specific and evidence-based to identify the population of patients who would benefit from glucarpidase.
高剂量甲氨蝶呤(HDMTX)引起的急性肾损伤是一种严重的、危及生命的毒性,可发生在儿科和成人患者中。葡醛内酯已获得美国食品和药物管理局批准,可用于肾功能障碍时高甲氨蝶呤浓度的治疗,但使用该药物的指南尚不清楚。一个专家小组被召集来提供具体的、专家共识指南,用于在发生 HDMTX 诱导的肾毒性和延迟甲氨蝶呤排泄的患者中使用葡醛内酯。该指南通过更准确地定义与开始 HDMTX 输注后几个时间点发生严重或危及生命的毒性风险相关的绝对甲氨蝶呤浓度,为识别可能受益于葡醛内酯解救的患者人群提供建议。对于 HDMTX 输注≤24 小时的患者,如果 36 小时浓度高于 30µM,42 小时浓度高于 10µM,或 48 小时浓度高于 5µM,且血清肌酐相对于基线测量值显著升高(表明 HDMTX 诱导的急性肾损伤),则可能需要使用葡醛内酯。在 36 至 42 小时 HDMTX 输注后,如果 48 小时甲氨蝶呤浓度高于 5µM,则可能需要使用葡醛内酯。葡醛内酯的给药应在 HDMTX 输注开始后 48-60 小时内最佳进行,因为在此时间点之后可能无法预防危及生命的毒性。
葡醛内酯是一种很少使用的药物,如果在接触高剂量甲氨蝶呤超过 60 小时后给予,其效果会降低,因此预测哪些患者需要它至关重要。目前尚无关于使用这种药物的共识指南。标签上的适应症没有给出具体的甲氨蝶呤浓度,超过该浓度就应该使用。一个国际专家组被召集来制定一个具体的、基于证据的共识指南,以确定哪些患者将受益于葡醛内酯。