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泼尼松和基因多态性对急性淋巴细胞白血病患儿依托泊苷处置的影响。

Effects of prednisone and genetic polymorphisms on etoposide disposition in children with acute lymphoblastic leukemia.

作者信息

Kishi Shinji, Yang Wenjian, Boureau Benoit, Morand Stanislas, Das Soma, Chen Peixian, Cook Edwin H, Rosner Gary L, Schuetz Erin, Pui Ching-Hon, Relling Mary V

机构信息

Department of Pharmaceutical Sciences, St Jude Children's Research Hospital, University of Tennessee, Memphis, TN 38105, USA.

出版信息

Blood. 2004 Jan 1;103(1):67-72. doi: 10.1182/blood-2003-06-2105. Epub 2003 Sep 11.

Abstract

Etoposide is a substrate for P-glycoprotein, CYP3A4, CYP3A5, and UGT1A1. Glucocorticoids modulate CYP3A and P-glycoprotein in preclinical models, but their effect on clinical etoposide disposition is unknown. We studied the pharmacokinetics of etoposide and its catechol metabolite in children with acute lymphoblastic leukemia, along with polymorphisms in CYP3A4, CYP3A5, MDR1, GSTP1, UGT1A1, and VDR. Plasma pharmacokinetics were assessed at day 29, after 1 month of prednisone (n = 102), and at week 54, without prednisone (n = 44). On day 29, etoposide clearance was higher (47.4 versus 29.2 mL/min/m2, P <.0001) than at week 54. The day 29 etoposide or catechol area under the curve (AUC) was correlated with neutropenia (P =.027 and P =.0008, respectively). The relationship between genotype and etoposide disposition differed by race and by prednisone use. The MDR1 exon 26 CC genotype predicted higher day 29 etoposide clearance (P =.002) for all patients, and the CYP3A5 AA and GSTP1 AA genotypes predicted lower clearance in blacks (P =.02 and.03, respectively). The UGT1A1 6/6, VDR intron 8 GG, and VDR Fok 1 CC genotypes predicted higher week 54 clearance in blacks (P =.039,.036, and.052, respectively). The UGT1A1 6/6 genotype predicted lower catechol AUC. Prednisone strongly induces etoposide clearance, genetic polymorphisms may predict the constitutive and induced clearance of etoposide, and the relationship between genotype and phenotype differs by race.

摘要

依托泊苷是P-糖蛋白、CYP3A4、CYP3A5和UGT1A1的底物。在临床前模型中,糖皮质激素可调节CYP3A和P-糖蛋白,但它们对临床依托泊苷处置的影响尚不清楚。我们研究了急性淋巴细胞白血病患儿中依托泊苷及其儿茶酚代谢物的药代动力学,以及CYP3A4、CYP3A5、MDR1、GSTP1、UGT1A1和VDR的多态性。在第29天(泼尼松治疗1个月后,n = 102)和第54周(未使用泼尼松,n = 44)评估血浆药代动力学。在第29天,依托泊苷清除率高于第54周(47.4对29.2 mL/min/m2,P <.0001)。第29天依托泊苷或儿茶酚的曲线下面积(AUC)与中性粒细胞减少相关(分别为P =.027和P =.0008)。基因型与依托泊苷处置之间的关系因种族和泼尼松使用情况而异。MDR1外显子26 CC基因型预测所有患者第29天依托泊苷清除率较高(P =.002),而CYP3A5 AA和GSTP1 AA基因型预测黑人清除率较低(分别为P =.02和.03)。UGT1A1 6/6、VDR内含子8 GG和VDR Fok 1 CC基因型预测黑人第54周清除率较高(分别为P =.039、.036和.052)。UGT1A1 6/6基因型预测儿茶酚AUC较低。泼尼松强烈诱导依托泊苷清除,基因多态性可能预测依托泊苷的固有和诱导清除,且基因型与表型之间的关系因种族而异。

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