Sasaki K, Tanaka J, Murakami T, Matuoka H, Fujimoto T, Taguchi H
Cancer Drug Deliv. 1985 Winter;2(1):77-86. doi: 10.1089/cdd.1985.2.77.
Clinical toxicities and pharmacokinetics of methotrexate (MTX), associated with reduced citrovorum factor (CF) neutralization, were studied on 279 infusions in 25 children with various malignancies. MTX, at 1000-8400 mg/m2, was infused during six to 24 hours with multiple schedules of reduced CF rescue. Plasma MTX levels ranged from 7.0 X 10(-5) to 7.0 X 10(-4) M during MTX infusion. The levels declined rapidly with a two-phase elimination pattern (t1/2 = 1.2-2.5 hours, t1/2 = 18-32 hours). The folate level in the plasma ranged from 5 X 10(-7) M to 1.4 X 10(-6) M when CF was administered every six hours or every three hours, respectively. Limited bone marrow suppression was seen in only seven percent of infusions, with moderate elevation of GOT and GPT in 20% of infusions, and stomatitis in only 2.6% of infusions, despite reduction in the total dose of CF from 225 mg to 105 mg and despite delaying CF initiation from nine hours to thirty-six hours after the start of MTX infusion.
对25例患有各种恶性肿瘤的儿童进行了279次甲氨蝶呤(MTX)输注,研究了与亚叶酸(CF)中和作用降低相关的MTX临床毒性和药代动力学。MTX剂量为1000 - 8400 mg/m²,在6至24小时内输注,并采用多种减少CF解救的方案。MTX输注期间血浆MTX水平在7.0×10⁻⁵至7.0×10⁻⁴ M之间。其水平以两相消除模式迅速下降(t1/2 = 1.2 - 2.5小时,t1/2 = 18 - 32小时)。当分别每6小时或每3小时给予CF时,血浆中叶酸水平在5×10⁻⁷ M至1.4×10⁻⁶ M之间。尽管CF总剂量从225 mg降至105 mg,且CF开始给药时间从MTX输注开始后9小时延迟至36小时,但仅7%的输注出现有限的骨髓抑制,20%的输注出现GOT和GPT中度升高,仅2.6%的输注出现口腔炎。