Pharmacokinetics of doxorubicin administered i.v. as Myocet (TLC D-99; liposome-encapsulated doxorubicin citrate) compared with conventional doxorubicin when given in combination with cyclophosphamide in patients with metastatic breast cancer

被引:92
作者
Swenson, CE
Bolcsak, LE
Batist, G
Guthrie, TH
Tkaczuk, KH
Boxenbaum, H
Welles, L
Chow, SC
Bhamra, R
Chaikin, P
机构
[1] Elan Pharmaceut Inc, Princeton, NJ 08540 USA
[2] McGill Univ, Jewish Gen Hosp, Clin Res Unit, Montreal, PQ H3T 1E2, Canada
[3] Univ Florida, Med Ctr, Jacksonville, FL 32209 USA
[4] Univ Maryland, Greenebaum Canc Ctr, Baltimore, MD 21201 USA
[5] Arishel Inc, N Potomac, MD USA
[6] StatPlus Inc, Yardley, PA USA
关键词
breast cancer; doxorubicin; liposomes; Myocet TLC D-99;
D O I
10.1097/00001813-200303000-00008
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Myocet (TLC D-99) is a liposomal formulation of the antineoplastic drug doxorubicin with an improved therapeutic index compared with conventional doxorubicin. The objective of this study was to assess the plasma disposition of doxorubicin when administered i.v. as TLC D-99 and to compare this to conventional drug. Metabolite (doxorubicinol) plasma levels were also quantitated in both treatment groups. Plasma was collected during the first course of treatment from 10 patients receiving TLC D-99 60 mg/m(2) and 10 receiving conventional doxorubicin 60 mg/m(2), each with cyclophosphamide 600 mg/m(2). Samples were assayed for total doxorubicin (all doxorubicin regardless of whether it is encapsulated or not), encapsulated doxorubicin (TLC D-99 group only) and doxorubicinol using high-performance liquid chromatography. Plasma concentrations of total doxorubicin were higher in patients receiving TLC D-99 than in patients receiving conventional doxorubicin. The clearance of total doxorubicin after administration of TLC D-99 was lower (approximately 9-fold) and the volume of distribution at steady state was less (25-fold) than that of doxorubicin after conventional drug. Doxorubicinol was detected in the plasma of all patients in both treatment groups. The mean AUC(0-infinity) of doxorubicinol for patients receiving TLC D-99 (1.5+/-0.4 muM.h) was not statistically different than that in patients receiving conventional doxorubicin (1.8+/-0.4 muM.h), although the appearance of the peak doxorubicinol concentration occurred later and was lower in patients receiving TLC D-99. There was a correlation between the plasma AUC(0-infinity) of total doxorubicin and the degree of myelosuppression in patients receiving conventional doxorubicin, but this correlation was not found in patients receiving TLC D-99.
引用
收藏
页码:239 / 246
页数:8
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