Schrøder H, Clausen N, Ostergaard E, Pressler T
Cancer Chemother Pharmacol. 1986;16(2):190-3. doi: 10.1007/BF00256175.
The concentration of methotrexate (MTX) in erythrocytes (E-MTX) was measured in 47 children with acute lymphoblastic leukemia during maintenance treatment with MTX 1.7-21.6 mg/m2/week and 6-mercaptopurine 25-75 mg/m2/day. At the time of measurement the plasma MTX concentration was less than 2 nmol/l. The steady state E-MTX varied between 51 and 202 nmol/l erythrocytes. Alterations in the E-MTX took place over 8-12 weeks after a change in dosage. A significant correlation was found between the E-MTX and the weekly dose of MTX administered. Noncompliance was revealed in two patients. A very low E-MTX was found in one patients, probably caused by inhibition of erythropoiesis. No correlation was found between E-MTX and the total amount of MTX administered or the length of treatment. A terminal half-life of 2-5 weeks after discontinuation of the drug showed that the erythrocytes functioned as a slow-changing compartment for MTX. Unexpectedly low E-MTX could mean noncompliance, impaired erythropoiesis, altered metabolism, or poor drug absorption.
对47例急性淋巴细胞白血病儿童在接受甲氨蝶呤(MTX)1.7 - 21.6毫克/平方米/周及6-巯基嘌呤25 - 75毫克/平方米/天维持治疗期间,测定了红细胞中甲氨蝶呤(E-MTX)的浓度。在测量时,血浆MTX浓度低于2纳摩尔/升。稳态E-MTX在红细胞中为51至202纳摩尔/升。剂量改变后8至12周,E-MTX发生变化。发现E-MTX与每周给予的MTX剂量之间存在显著相关性。两名患者被发现存在不依从情况。一名患者的E-MTX非常低,可能是由于红细胞生成受抑制所致。未发现E-MTX与给予的MTX总量或治疗时长之间存在相关性。停药后2至5周的终末半衰期表明,红细胞对MTX起到了一个变化缓慢的隔室的作用。E-MTX意外偏低可能意味着不依从、红细胞生成受损、代谢改变或药物吸收不良。