Neoplasma. 2014;61(1):77-82.
Methotrexate (MTX) is an effective treatment for childhood acute lymphoblastic leukemia (ALL) or Non-Hodgkin lymphoma (NHL); however, toxicity can arise with high doses MTX (HDMTX), especially in patients with delayed MTX elimination. Routine monitoring of plasma MTX concentrations is clinically important, but unfortunately is not always feasible. The aim of this study was to examine the relationship between MTX elimination and renal function to identify parameters that may be useful for predicting delayed MTX elimination in Chinese children with ALL and NHL. A total of 105 children with ALL and NHL were included in the study. Each patient received HDMTX (3 or 5 g/m2) over 24 hours. Plasma MTX concentrations were measured at 24, 48, and 96 hours. Delayed elimination was indicated by plasma MTX concentrations ≥1.0 at 48 hours or ≥0.1 μmol/L at 96 hours. Creatinine clearance rate (CCr) and serum Cr concentrations were measured at 0, 24, and 48 hours. There were 39 patients (37.1%) with delayed MTX elimination. For patients with delayed MTX elimination, the 24 hour plasma MTX concentration was negatively correlated with the 24 hour CCr (P=0.019). The 48 hour plasma MTX concentration was positively correlated with 24 and 48 hour serum Cr concentrations (P=0.001 and P<0.001, respectively), and negatively correlated with the 24 and 48 CCr (both P<0.001). Both MTX concentrations and elimination time decreased with increasing CCr (P<0.05 and P<0.001, respectively). Receiver operating characteristic curves revealed that the best predictors of delayed MTX elimination were 24 hour CCr 36 mmol/L (sensitivity: 64.7%; specificity: 77.4%) (both P < 0.001). CCr and serum Cr concentration may be useful for monitoring plasma MTX concentrations in children receiving HDMTX for ALL and NHL and for predicting delayed MTX elimination.
甲氨蝶呤(MTX)是治疗儿童急性淋巴细胞白血病(ALL)或非霍奇金淋巴瘤(NHL)的有效药物;然而,大剂量甲氨蝶呤(HDMTX)会引起毒性,特别是在 MTX 消除延迟的患者中。临床中,监测血浆 MTX 浓度非常重要,但遗憾的是并不总是可行。本研究旨在探讨 MTX 消除与肾功能之间的关系,以确定可能有助于预测中国 ALL 和 NHL 患儿 MTX 消除延迟的参数。共纳入 105 例 ALL 和 NHL 患儿。每位患者接受 3 或 5 g/m2 的 HDMTX,24 小时内输注完毕。分别在 24、48 和 96 小时测定血浆 MTX 浓度。48 小时时血浆 MTX 浓度≥1.0μmol/L 或 96 小时时血浆 MTX 浓度≥0.1μmol/L 提示 MTX 消除延迟。在 0、24 和 48 小时时测定肌酐清除率(CCr)和血清 Cr 浓度。有 39 例(37.1%)患儿发生 MTX 消除延迟。对于 MTX 消除延迟的患儿,24 小时血浆 MTX 浓度与 24 小时 CCr 呈负相关(P=0.019)。48 小时血浆 MTX 浓度与 24 小时和 48 小时血清 Cr 浓度呈正相关(P=0.001 和 P<0.001),与 24 小时和 48 小时 CCr 呈负相关(均 P<0.001)。MTX 浓度和消除时间均随 CCr 增加而降低(P<0.05 和 P<0.001)。受试者工作特征曲线显示,预测 MTX 消除延迟的最佳指标是 24 小时 CCr 36mmol/L(灵敏度:64.7%;特异性:77.4%)(均 P<0.001)。CCr 和血清 Cr 浓度可能有助于监测接受 ALL 和 NHL 患儿 HDMTX 治疗时的血浆 MTX 浓度,并预测 MTX 消除延迟。