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大剂量甲氨蝶呤化疗治疗局限性骨肉瘤的药代动力学个体化

Pharmacokinetic individualization of high-dose methotrexate chemotherapy for the treatment of localized osteosarcoma.

作者信息

Fujita Y, Nakamura T, Aomori T, Nishiba H, Shinozaki H, Yanagawa T, Takagishi K, Watanabe H, Okada Y, Nakamura K, Horiuchi R, Yamamoto K

机构信息

Department of Pharmacy, Gunma University Hospital, Gunma, Japan.

出版信息

J Chemother. 2010 Jun;22(3):186-90. doi: 10.1179/joc.2010.22.3.186.

Abstract

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.

摘要

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。

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