Methodology and limits of preclinical evaluation during the development of anticancer drug combinations

被引:0
|
作者
Vassal, G
机构
[1] Inst Gustave Roussy, Dept Pediat, F-94805 Villejuif, France
[2] Inst Gustave Roussy, Lab Pharmacotoxicol & Pharmacogenet, CNRS, UMR 1772, F-94805 Villejuif, France
关键词
synergism; additivity; antagonism;
D O I
暂无
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
In chemosensitive tumors, cancer chemotherapy is active as drug combinations. During the development of new anticancer drugs, preclinical experimental models may help to design drug combinations. Indeed, in vitro models are able to define drug interactions in terms of synergism, additivity or antagonism, while in vivo models can evaluate therapeutic synergism along with toxicity in a clinical setting. The methodology for in vitro and in vivo evaluation of anticancer drug combinations is described. The limits are discussed. In conclusion, preclinical models contribute to the clinical therapeutic principles.
引用
收藏
页码:929 / 934
页数:6
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