Pharmacokinetics of rituximab and its clinical use: Thought for the best use?

被引:108
作者
Cartron, Guillaume
Blasco, Helene
Paintaud, Gilles
Watier, Herve
Le Guellec, Chantal
机构
[1] Univ Tours, UPRESEA 3853 Immuno Pharmaco Genet Anticorps Ther, IPGA, F-37032 Tours 1, France
[2] Ctr Jean Bernard, Le Mans, France
[3] CHRU Tours, Lab Pharmacol Toxicol, Tours, France
[4] CHRU Tours, Immunol Lab, Tours, France
关键词
rituximab; pharmacokinetics; treatment optimisation;
D O I
10.1016/j.critrevonc.2006.09.004
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Rituximab (MabThera((R)), Rituxan((R))) is a chimaeric monoclonal antibody increasingly used in the treatment of B-lymphoproliferative disorders and autoimmune diseases. Rituximab is now associated with chemotherapy for the treatment of non-Hodgkin's lymphoma and should be approved soon in maintenance strategies. During its rapid clinical development, rituximab schedules were dictated more often by logistical rather than by scientific considerations. In addition, early clinical phases have shown that rituximab exposure was variable in patients receiving similar doses and that clinical response was related to rituximab concentrations. There is however limited information on rituximab pharmacokinetics and on factors influencing individual exposure to this monoclonal antibody, although a better understanding of these factors is needed to optimise its dosing regimen. This review focuses on the current knowledge on rituximab pharmacokinetics and on factors influencing individual exposure and suggests ways to improve its clinical use. (c) 2007 Published by Elsevier Ireland Ltd.
引用
收藏
页码:43 / 52
页数:10
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