Greenmyer Jacob R, Burd Larry, Kobrinsky Nathan L
J Pediatr Pharmacol Ther. 2021;26(3):300-305. doi: 10.5863/1551-6776-26.3.300. Epub 2021 Mar 31.
Early identification of methotrexate-induced acute kidney injury (AKI) and delayed elimination of methotrexate are critical to limiting toxicity of the drug. The current monitoring strategy consists of serial serum methotrexate concentrations at 24, 36, 42, and 48 hours. Appropriate serum concentration monitoring and intervention does not always prevent AKI. Therefore, ongoing study of biomarkers and improved methods of screening for methotrexate-induced AKI is critical to reduce toxicity. This case series reports urine methotrexate values of 4 patients undergoing treatment with high-dose methotrexate. Urine methotrexate concentration was measured 46 to 48 hours after methotrexate infusion. Urine methotrexate concentration was compared with the duration of drug clearance from the serum. Only 1 patient (case 3) developed AKI. Serum concentration of methotrexate were < 0.3 μmol/L at 42, 48, and 48 hours in patients 1, 2, and 4, respectively, and at 168 hours in patient 3 (p < 0.01). Urine methotrexate concentrations were 2.77, 6.45, and 7.8 (μmol/L), in patients 1, 2, and 4, respectively, and 113.69 (μmol/L) in patient 3 (p < 0.001). This case series provides preliminary data that urine methotrexate concentration at hours 46 to 48 may reflect AKI. Future studies should investigate the ability of serial urine methotrexate concentrations to predict delayed drug clearance and the development of AKI.
早期识别甲氨蝶呤诱导的急性肾损伤(AKI)以及延缓甲氨蝶呤的清除对于限制该药物的毒性至关重要。当前的监测策略包括在24、36、42和48小时测定血清甲氨蝶呤浓度。适当的血清浓度监测和干预并不总能预防AKI。因此,持续研究生物标志物以及改进甲氨蝶呤诱导的AKI筛查方法对于降低毒性至关重要。本病例系列报告了4例接受高剂量甲氨蝶呤治疗患者的尿甲氨蝶呤值。在甲氨蝶呤输注后46至48小时测量尿甲氨蝶呤浓度。将尿甲氨蝶呤浓度与药物从血清中清除的持续时间进行比较。仅1例患者(病例3)发生了AKI。患者1、2和4在42、48和48小时时血清甲氨蝶呤浓度分别<0.3μmol/L,患者3在168小时时血清甲氨蝶呤浓度<0.3μmol/L(p<0.01)。患者1、2和4的尿甲氨蝶呤浓度分别为2.77、6.45和7.8(μmol/L),患者3的尿甲氨蝶呤浓度为113.69(μmol/L)(p<0.001)。本病例系列提供了初步数据,表明在46至48小时时尿甲氨蝶呤浓度可能反映AKI。未来的研究应调查连续尿甲氨蝶呤浓度预测药物清除延迟和AKI发生的能力。