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甲氨蝶呤在骨肉瘤中的药代动力学与生存率

Methotrexate pharmacokinetics and survival in osteosarcoma.

作者信息

Aquerreta Irene, Aldaz Azucena, Giráldez Joaquín, Sierrasesúmaga Luis

机构信息

Department of Pharmacy, University Hospital of Navarra, Pamplona, Spain.

出版信息

Pediatr Blood Cancer. 2004 Jan;42(1):52-8. doi: 10.1002/pbc.10443.

Abstract

BACKGROUND

The aim of this study was to analyze the relationship between exposure to high-dose methotrexate (HDMTX) and tumor response in terms of survival in children with osteosarcoma.

PROCEDURE

This study included 44 patients (479 courses) who received a median dose of 5.92 g/m2 of MTX (interquartile range (IQR) 2.37 g/m2) in a 4-hr infusion. The mean area under the concentration-time curve (AUC) estimated by parametric methods (non-parametric expectation maximization, NPEM), and the mean concentration at the end of the infusion were considered to be the exposure parameters. Tumor response was recorded as disease-free survival (DFS), overall survival (OS), and histologic tumor response. The relationship between MTX exposure and survival parameters was analyzed by Cox regression.

RESULTS

The group of 11 patients who were the least exposed to MTX (AUC <2,400 micromol/L hr) presented a high DFS, probably due to the shorter interval of time between MTX courses that led to a higher dose density. In patients with AUC >2,400 micromol/L hr, an increase in the AUC was related to an increase in the DFS. Significant differences were observed in the DFS between patients whose mean AUC was below or above 4,000 micromol/L hr (P=0.024), such that 4,000 micromol/L hr was considered as the minimum AUC to be aimed at for future patients.

CONCLUSIONS

Dose density seems to be an important factor in osteosarcoma response, but this must be confirmed in further studies. In order to improve the response to osteosarcoma in children, it is recommended that the dose of MTX to be increased such as to obtain an AUC higher than 4,000 micromol/L hr.

摘要

背景

本研究旨在分析骨肉瘤患儿中高剂量甲氨蝶呤(HDMTX)暴露与肿瘤反应在生存方面的关系。

程序

本研究纳入了44例患者(479个疗程),这些患者在4小时输注中接受的甲氨蝶呤中位剂量为5.92 g/m²(四分位间距(IQR)为2.37 g/m²)。通过参数方法(非参数期望最大化,NPEM)估计的浓度-时间曲线下平均面积(AUC)以及输注结束时的平均浓度被视为暴露参数。肿瘤反应记录为无病生存期(DFS)、总生存期(OS)和组织学肿瘤反应。通过Cox回归分析甲氨蝶呤暴露与生存参数之间的关系。

结果

甲氨蝶呤暴露最少的11例患者组(AUC<2400微摩尔/升·小时)呈现出较高的DFS,这可能是由于甲氨蝶呤疗程之间的时间间隔较短,导致剂量密度较高。在AUC>2400微摩尔/升·小时的患者中,AUC的增加与DFS的增加相关。平均AUC低于或高于4000微摩尔/升·小时的患者之间的DFS存在显著差异(P = 0.024),因此4000微摩尔/升·小时被视为未来患者应达到的最低AUC。

结论

剂量密度似乎是骨肉瘤反应中的一个重要因素,但这必须在进一步研究中得到证实。为了提高儿童骨肉瘤的反应,建议增加甲氨蝶呤的剂量,以获得高于4000微摩尔/升·小时的AUC。

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