Fujita Y, Nakamura T, Aomori T, Nishiba H, Shinozaki H, Yanagawa T, Takagishi K, Watanabe H, Okada Y, Nakamura K, Horiuchi R, Yamamoto K
Department of Pharmacy, Gunma University Hospital, Gunma, Japan.
J Chemother. 2010 Jun;22(3):186-90. doi: 10.1179/joc.2010.22.3.186.
Individualization of high-dose methotrexate (MTX) dosing is important to achieve therapeutic levels (700-1,000 microM) for osteosarcoma. Therefore we developed a pharmacokinetically (PK) individualized dosage regimen to maintain MTX concentrations of 700 microM (1 h bolus followed by 5 h maintenance infusion) and evaluated its safety and efficacy. Loading and maintenance doses were calculated by the PK parameters based on 2-compartment model analysis. Thirty-two courses of chemotherapy were performed in 9 patients with osteosarcoma. The maximum concentrations during maintenance infusion in 31 courses (97%) were above 700 microM. Only 1 patient developed severe hepatotoxicity as adverse effect. Total body clearance of MTX decreased in 4 patients when weekly MTX chemotherapy was performed for 3 consecutive weeks. Although the clearance was changed, the average MTX concentrations were maintained at about 700 microM by the PK individualization. The 5-year survival rate was 77.8% (7 of 9 patients), and all of them have survived for more than 9 years. This PK individualization is safe and useful for tailoring high-dose MTX therapy to achieve therapeutic levels.
高剂量甲氨蝶呤(MTX)给药个体化对于骨肉瘤达到治疗水平(700 - 1000微摩尔)很重要。因此,我们制定了一种基于药代动力学(PK)的个体化给药方案,以维持MTX浓度在700微摩尔(1小时推注后接着5小时维持输注),并评估其安全性和有效性。负荷剂量和维持剂量根据基于二室模型分析的PK参数计算得出。对9例骨肉瘤患者进行了32个疗程的化疗。31个疗程(97%)维持输注期间的最高浓度高于700微摩尔。只有1例患者出现严重肝毒性作为不良反应。当连续3周每周进行MTX化疗时,4例患者的MTX全身清除率下降。尽管清除率发生了变化,但通过PK个体化,MTX的平均浓度维持在约700微摩尔。5年生存率为77.8%(9例患者中的7例),并且他们全部存活超过9年。这种PK个体化对于定制高剂量MTX治疗以达到治疗水平是安全且有用的。