Ikeda H, Kihira K, Kuwata N, Arai S, Kimura Y, Miyake K, Kitaura T, Fujimura K, Kuramoto A, Fukuchi H
Department of Pharmaceutical Services, Hiroshima University Hospital, Japan.
Hiroshima J Med Sci. 1996 Jun;45(2):57-62.
The purpose of this study was to identify the patients with decreased methotrexate (MTX) clearance as early as possible after the start of high-dose methotrexate (HD-MTX) infusion. Fifty-six patients (age: 18 approximately 83 years) received a HD-MTX infusion (dosage: 1.9 approximately 3.8 g/m2) for 6 h. These patients were retrospectively divided into a low-clearance group and a high-clearance group based on the serum MTX concentration at 48 h (1 microM). Six out of the 56 patients showed decreased MTX clearance. The MTX concentrations in the low-clearance group were significantly higher than those in the high-clearance group even in earlier sampling times than at 48 h. The average MTX concentrations were 330 microM at 6 h, 72 microM at 12 h, and 16 microM at 24 h in the low-clearance group, and those in the high-clearance group were 210 microM, 18 microM, and 1.0 microM, respectively. The estimated elimination half-lives (t1/2) at 6 approximately 12 h and 12 approximately 24 h after the start of the infusion were also significantly longer in the low-clearance group (2.8 vs. 1.7 h and 5.0 vs. 2.8 h, respectively). Therefore, we proposed convenient criteria based on the mean + 1 S.D. of the high-clearance group: the concentration > 270 microM at 6 h and > 32 microM at 12 h; the t1/2 value > 2.1 h at 6-12 h. All 6 patients were recognized as belonging to the low-clearance group at an early stage after HD-MTX infusion by using our proposed criteria. These results indicate that patients with decreased MTX clearance could be identified within the first 12 h after the start of HD-MTX infusion. The factors influencing the prolonged elimination of MTX were also investigated. A significant decrease in renal function on day 2 was observed in the low-clearance group. The MTX level at 12 h and the estimated t1/2 values were significantly correlated with BUN, Scr and Clcr on the 2nd day after HD-MTX therapy, suggesting that an alteration in renal function occurs within 12 h of the HD-MTX infusion. The prolonged elimination of MTX could be attributable to this decrease in renal function.
本研究的目的是在大剂量甲氨蝶呤(HD-MTX)输注开始后尽早识别甲氨蝶呤(MTX)清除率降低的患者。56例患者(年龄:18至83岁)接受了6小时的HD-MTX输注(剂量:1.9至3.8 g/m²)。根据48小时时的血清MTX浓度(1微摩尔/升)将这些患者回顾性分为低清除率组和高清除率组。56例患者中有6例显示MTX清除率降低。即使在早于48小时的采样时间,低清除率组的MTX浓度也显著高于高清除率组。低清除率组在6小时、12小时和24小时时的平均MTX浓度分别为330微摩尔/升、72微摩尔/升和16微摩尔/升,高清除率组分别为210微摩尔/升、18微摩尔/升和1.0微摩尔/升。输注开始后6至12小时和12至24小时的估计消除半衰期(t1/2)在低清除率组中也显著更长(分别为2.8小时对1.7小时和5.0小时对2.8小时)。因此,我们根据高清除率组的均值 + 1标准差提出了方便的标准:6小时时浓度 > 270微摩尔/升且12小时时 > 32微摩尔/升;6至12小时时t1/2值 > 2.1小时。使用我们提出的标准,所有6例患者在HD-MTX输注后的早期阶段均被识别为属于低清除率组。这些结果表明,在HD-MTX输注开始后的前12小时内可以识别出MTX清除率降低的患者。还研究了影响MTX消除延长的因素。在低清除率组中观察到第2天肾功能显著下降。HD-MTX治疗后第2天,12小时时的MTX水平和估计的t1/2值与血尿素氮、血清肌酐和肌酐清除率显著相关,表明在HD-MTX输注后12小时内肾功能发生改变。MTX消除延长可能归因于肾功能的这种下降。