Effect of ABCG2 genotype on the oral Bioavailability of topotecan

被引:119
作者
Sparreboom, A
Loos, WJ
Burger, H
Sissung, TM
Verweij, J
Figg, WD
Nooter, K
Gelderblom, H
机构
[1] Erasmus MC, Dr Daniel Den Hoed Canc Ctr, Dept Med Oncol, Josephine Nefkens Inst, NL-3075 EA Rotterdam, Netherlands
[2] NCI, Clin Pharmacol Res Core, Bethesda, MD 20892 USA
[3] Leiden Univ, Med Ctr, Dept Clin Oncol, Leiden, Netherlands
关键词
topotecan; ABCG2; pharmacokinetics; pharmacogenetics; accumulation; mutant; in vitro;
D O I
10.4161/cbt.4.6.1731
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
ABCG2 ( BCRP/MXR/ABCP) functions as an efflux transporter for many agents, including topotecan, and the protein is expressed at high levels in the human intestine. Some individuals possess a nonsynonymous variant in the ABCG2 gene at nucleotide 421, substituting Lysine for Glutamine on position 141 at exon 5. The present pilot study indicates that this genotype results in a 30% reduced efflux transport of topotecan in vitro compared to the wild-type. In a preliminary fashion, the heterozygous CA allele observed in two patients was associated with a 1.34-fold increased oral bioavailability of topotecan compared to the bioavailability in ten patients with the wild-type allele (42.0% versus 31.4%; P = 0.037). It is suggested that the high frequency of the A allele in certain ethnic groups may have therapeutic implications for individuals treated with topotecan or other ABCG2 substrates.
引用
收藏
页码:650 / 653
页数:4
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