Cohen H J, Jaffe N
Cancer Chemother Pharmacol. 1978;1(1):61-4. doi: 10.1007/BF00253148.
Cytocidal activity of a drug is dependent on both drug dosage and duration of exposure. In contrast to the 'conventional" 6-h infusion and in an attempto to improve its efficacy, the high-dose methotrexate therapeutic regimen was given over a 24-h period with 10% of the dose administered in the first hour. Citrovorum factor was initiated at hour 24 and continued for 72 h. Treatment was administered every 2-3 weeks. 57 infusions were performed in twelve patients aged 7-20 years (six with osteogenic sarcoma and six with acute lymphoblastic leukemia). Determinations of serum methotrexate levels revealed that the levels were dependent on the dose. Levels assayed at 24 h revealed the following results: 4.4 +/- 1.4 x 10(-5) molar with 4.5 g/m(2), 2.04 +/- 0.34 x 10(-4) molar with 7.5 g/m(2) and 4.59 +/- 0.80 x 10(-4) molar with 12.5 g/m(2). Major toxicity was myelosuppression in 12 of 57 patients. There were no responses. The study demonstrates that 24-h infusions of high-dose methotrexate can be tolerated every 2-3 weeks in patients without bone marrow involvement and levels of at least 10(-4) molar can be maintained during the infusion.
药物的细胞杀伤活性取决于药物剂量和暴露持续时间。与“传统的”6小时输注不同,为提高其疗效,高剂量甲氨蝶呤治疗方案在24小时内给药,其中10%的剂量在第1小时给予。亚叶酸在第24小时开始使用,并持续72小时。每2至3周进行一次治疗。对12名年龄在7至20岁的患者(6例骨肉瘤患者和6例急性淋巴细胞白血病患者)进行了57次输注。血清甲氨蝶呤水平测定显示,其水平取决于剂量。在24小时时测定的水平显示以下结果:4.5g/m²时为4.4±1.4×10⁻⁵摩尔,7.5g/m²时为2.04±0.34×10⁻⁴摩尔,12.5g/m²时为4.59±0.80×10⁻⁴摩尔。57例患者中有12例出现的主要毒性为骨髓抑制。未观察到缓解情况。该研究表明,对于无骨髓受累的患者,每2至3周进行一次24小时高剂量甲氨蝶呤输注是可以耐受的,并且在输注期间可维持至少10⁻⁴摩尔的水平。