高剂量甲氨蝶呤治疗儿童恶性肿瘤的减少citrovorum因子挽救。

K Sasaki, J Tanaka, T Murakami, H Matuoka, T Fujimoto, H Taguchi
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引用次数: 10

摘要

本文对25例不同恶性肿瘤患儿279次输注甲氨蝶呤(MTX)的临床毒性和药代动力学进行了研究。MTX剂量为1000-8400 mg/m2,在6 - 24小时内输注,并伴有减少CF抢救的多个时间表。在MTX输注期间,血浆MTX水平从7.0 X 10(-5)到7.0 X 10(-4) M不等。呈两期消除模式(t1/2 = 1.2 ~ 2.5 h, t1/2 = 18 ~ 32 h)迅速下降。当每6小时或每3小时给予CF时,血浆中叶酸水平分别为5 × 10(-7) M至1.4 × 10(-6) M。尽管CF的总剂量从225mg降低到105mg,并且在MTX开始输注后将CF的起始时间从9小时延迟到36小时,但只有7%的输注者出现了有限的骨髓抑制,20%的输注者出现了GOT和GPT的中度升高,只有2.6%的输注者出现了口炎。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Reduced citrovorum factor rescue for high-dose methotrexate therapy in childhood malignancies.

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.

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