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一名股骨恶性纤维组织细胞瘤患者在大剂量甲氨蝶呤治疗期间的连续瘤内微透析:病例报告

Continuous intratumoral microdialysis during high-dose methotrexate therapy in a patient with malignant fibrous histiocytoma of the femur: a case report.

作者信息

Ekstrøm P O, Andersen A, Saeter G, Giercksky K E, Slørdal L

机构信息

Department of Surgical Oncology, Norwegian Radium Hospital, Oslo, Norway.

出版信息

Cancer Chemother Pharmacol. 1997;39(3):267-72. doi: 10.1007/s002800050571.

Abstract

We used a microdialysis technique to assay intratumoral methotrexate (MTX) levels during high-dose (12 g/m2 given as a 4-h infusion) therapy in a 43-year-old man with a malignant fibrous histiocytoma in the medial femoral condyle. Additional microdialysis probes were implanted in muscle tissue contralateral to the tumor and in an antecubital vein. Microdialysis was attempted during the initial two high-dose courses, but the two latter probes were removed at the start of the second treatment cycle due to leakage. No attempt to correct for microdialysis recovery was made. The intratumorally localized probe gave reproducible data on tumor MTX exposure of 9.3-14% of unbound systemic MTX. There was a close correlation between tumor and systemic levels for both MTX and its major extracellular metabolite 7-hydroxymethotrexate. Although limited to the study of MTX pharmacokinetics in a single subject, the experiment demonstrates that intratumoral microdialysis may provide data on tumor drug exposure, although of an indirect nature and dependent on the probe characteristics, the flow rate, and, possibly, the time after probe implantation. We propose that the application of microdialysis may prove useful for elucidation of the relationship between local drug exposure and the therapeutic response in normally inaccessible compartments during cancer pharmacotherapy.

摘要

我们采用微透析技术,对一名43岁、患有股骨内侧髁恶性纤维组织细胞瘤的男性患者在高剂量(12 g/m²,4小时静脉输注)治疗期间的肿瘤内甲氨蝶呤(MTX)水平进行了测定。在肿瘤对侧的肌肉组织和肘前静脉中植入了额外的微透析探针。在前两个高剂量疗程中尝试进行微透析,但由于渗漏,后两个探针在第二个治疗周期开始时被移除。未尝试对微透析回收率进行校正。肿瘤内定位的探针给出了关于肿瘤MTX暴露量的数据,其为未结合的全身MTX的9.3 - 14%,且具有可重复性。MTX及其主要细胞外代谢产物7 - 羟基甲氨蝶呤的肿瘤水平与全身水平之间存在密切相关性。尽管该实验仅限于对单一受试者的MTX药代动力学研究,但它表明肿瘤内微透析可能提供关于肿瘤药物暴露的数据,尽管其性质是间接的,且依赖于探针特性、流速以及可能还依赖于探针植入后的时间。我们认为,微透析的应用可能有助于阐明癌症药物治疗期间,在通常难以接近的区域中局部药物暴露与治疗反应之间的关系。

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