Large-scale imatinib dose-concentration-effect study in CML patients under routine care conditions

被引:45
作者
Gotta, Verena [1 ,2 ,3 ]
Bouchet, Stephane [4 ]
Widmer, Nicolas [1 ,2 ]
Schuld, Peter [5 ]
Decosterd, Laurent A. [2 ,6 ]
Buclin, Thierry [1 ,2 ]
Mahon, Francois-Xavier [7 ]
Csajka, Chantal [1 ,2 ,3 ]
Molimard, Mathieu [5 ]
机构
[1] CHU Vaudois, Div Clin Pharmacol, Serv Biomed, CH-1005 Lausanne, Switzerland
[2] Univ Lausanne, Lausanne, Switzerland
[3] Univ Lausanne, Univ Geneva, Sch Pharmaceut Sci, Geneva, Switzerland
[4] Ctr Hosp Univ Bordeaux, Dept Clin Pharmacol & Toxicol, Bordeaux, France
[5] Novartis Oncol Reg Europe, Milan, Italy
[6] CHU Vaudois, Serv Biomed, Innovat & Dev Unit, Lab Clin Pharmacol, CH-1005 Lausanne, Switzerland
[7] Univ Bordeaux 2, Lab Hematopoise Leucem & Cible Therapeut, F-33076 Bordeaux, France
基金
瑞士国家科学基金会;
关键词
Tyrosine kinase inhibitor; Pharmacokinetics; Pharmacodynamics; Therapeutic drug monitoring; Drug monitoring; Chronic myelogenous leukemia; Dose-response relationship; CHRONIC MYELOID-LEUKEMIA; DRUG-INTERACTIONS; POPULATION PHARMACOKINETICS; PLASMA-CONCENTRATIONS; INHIBITION; MESYLATE; OUTCOMES; THERAPY;
D O I
10.1016/j.leukres.2014.03.023
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
This observational study analyzed imatinib pharmacokinetics and response in 2478 chronic myeloid leukemia (CML) patients. Data were obtained through centralized therapeutic drug monitoring (TDM) at median treatment duration of >= 2 years. First, individual initial trough concentrations under 400 mg/day imatinib starting dose were estimated. Second, their correlation ((C) over cap (min(400) (mg))) with reported treatment response was verified. Low imatinib levels were predicted in young male patients and those receiving P-gp/CYP3A4 inducers. These patients had also lower response rates (7% lower 18-months MMR in male, 17% lower 1-year CCyR in young patients, Kaplan-Meier estimates). Time-point independent multivariate regression confirmed a correlation of individual (C) over cap (min(400 mg)) with response and adverse events. Possibly due to confounding factors (e.g. dose modifications, patient selection bias), the relationship seemed however flatter than previously reported from prospective controlled studies. Nonetheless, these observational results strongly suggest that a subgroup of patients could benefit from early dosage optimization assisted by TDM, because of lower imatinib concentrations and lower response rates. (C) 2014 Elsevier Ltd. All rights reserved.
引用
收藏
页码:764 / 772
页数:9
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