Jaffe N, Prudich J, Knapp J, Wang Y M, Bowman R, Cangir A, Ayala A, Chuang V, Wallace S
J Clin Oncol. 1983 Jul;1(7):428-31. doi: 10.1200/JCO.1983.1.7.428.
In an effort to achieve high concentrations and prolonged exposure times, high-dose methotrexate (MTX) was administered by the intra-arterial route over 6 hours at a dose of 12.5 g/m2 to nine patients with osteosarcoma. This was followed by citrovorum factor (CF) rescue, which was initiated 12 hours after completion of the infusion (MTX-CF). The regimen achieved high local concentrations over a finite period. No toxicity was encountered. Treatment was administered at weekly intervals, during which intravenous MTX-CF was interposed if facilities for intra-arterial administration were not available. However, despite increases in local venous concentrations and exposure times, only four of nine patients (44%) responded. This is similar to responses achieved with 7.5 g/m2 (48%) with CF initiated 2 hours after completion of the infusion. Higher MTX doses, intra-arterial administration, and prolongation of cytotoxic exposure time did not confer a therapeutic advantage as opposed to "conventional" intravenous high doses.
为了达到高浓度和延长暴露时间,对9例骨肉瘤患者采用动脉内途径在6小时内给予大剂量甲氨蝶呤(MTX),剂量为12.5 g/m²。随后进行亚叶酸钙(CF)解救,在输注完成后12小时开始(MTX - CF)。该方案在有限时间内达到了高局部浓度。未出现毒性反应。治疗每周进行一次,如果没有动脉内给药设备,则在其间插入静脉内MTX - CF。然而,尽管局部静脉浓度和暴露时间有所增加,但9例患者中只有4例(44%)有反应。这与输注完成后2小时开始CF、剂量为7.5 g/m²时的反应率(48%)相似。与“传统”静脉高剂量相比,更高的MTX剂量、动脉内给药以及延长细胞毒性暴露时间并未带来治疗优势。