摘要
多西他赛广泛用于乳腺癌、非小细胞肺癌、前列腺癌等多种肿瘤的治疗,然而,多西他赛临床疗效和不良反应的个体差异近年来受到越来越多的关注,国内外相关文献提示药物代谢相关基因的遗传变异是导致个体差异的重要原因之一。本文就细胞色素P450酶、多药耐药基因、药物转运体的基因多态性与多西他赛在体内的药代动力学/药效学个体差异及其与临床疗效与不良反应的相关性做一综述。
Docetaxel is widely used in the treatment of breast cancer,non- small cell lung cancer,prostate cancer and other cancer.However,individual differences in clinical efficacy and adverse drug reactions of docetaxel have attracted more and more attention in recent years.Domestic and foreign literatures have suggested that the genetic variation of drug metabolism related genes is one of the important reasons leading to individual differences.In this paper,correlations between genetic polymorphism of cytochrome P450 enzymes,multidrug resistance gene,drug transporters of docetaxel and individual difference of pharmacokinetics/pharmacodynamics,clinical efficacy and adverse drug reactions of duoxetacel are reviewed.
出处
《中国临床药理学杂志》
CAS
CSCD
北大核心
2015年第24期2486-2488,2491,共4页
The Chinese Journal of Clinical Pharmacology
基金
江苏省药学会奥赛康临床药学研究课题基金资助项目(KY201379)
常州市青年医学创新人才项目基金资助项目(KY201132)