Methotrexate area under the curve is an important outcome predictor in patients with primary CNS lymphoma: A pharmacokinetic-pharmacodynamic analysis from the IELSG no. 20 trial

被引:69
|
作者
Joerger, M. [1 ]
Huitema, A. D. R. [2 ]
Kraehenbuehl, S. [3 ]
Schellens, J. H. M. [4 ,5 ]
Cerny, T. [1 ]
Reni, M. [6 ]
Zucca, E. [7 ]
Cavalli, F. [7 ]
Ferreri, A. J. M. [6 ,8 ]
机构
[1] Cantonal Hosp, Dept Hematol & Oncol, CH-9007 St Gallen, Switzerland
[2] Slotervaart Hosp, Netherlands Canc Inst, Dept Pharm & Pharmacol, NL-1066 CX Amsterdam, Netherlands
[3] Univ Hosp, Div Clin Pharmacol & Toxicol, CH-4056 Basel, Switzerland
[4] Antoni Van Leeuwenhoek Hosp, Netherlands Canc Inst, Dept Med Oncol, NL-1066 CX Amsterdam, Netherlands
[5] Univ Utrecht, FAFC Wentgebouw, Fac Pharmaceut Sci, Div Drug Toxicol,Dept Biomed Anal, NL-3584 CA Utrecht, Netherlands
[6] Ist Sci San Raffaele, Dept Oncol, Med Oncol Unit, I-20132 Milan, Italy
[7] Oncol Inst So Switzerland, CH-6500 Bellinzona, Switzerland
[8] Ist Sci San Raffaele, Dept Oncol, Unit Lymphoid Malignancies, I-20132 Milan, Italy
关键词
methotrexate; high-dose chemotherapy; CNS lymphoma; cytarabine; pharmacokinetics; DRUG-INTERACTIONS; SYSTEM; CLEARANCE;
D O I
10.1038/sj.bjc.6605559
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
BACKGROUND: This analysis was initiated to define the predictive value of the area under the curve of high-dose methotrexate (AUC(HD-MTX)) in patients with primary central nervous system lymphoma (PCNSL). PATIENTS AND METHODS: We included 55 patients with PCNSL and available pharmacokinetic (PK) data from the International Extranodal Lymphoma Study Group (IELSG) no. 20 trial, randomised to HD-MTX (n = 30) or HD-MTX and high-dose cytarabine (HD-AraC) (n = 25). Individual AU(CHD-MTX) from population PK analysis was tested on drug toxicity and clinical outcome using multivariate logistic regression analysis and Cox hazards modelling. RESULTS: AUC(HD-MTX), the IELSG score and treatment group were significant predictors for treatment response (complete or partial) in the adjusted model. The AU(CHD-MTX) did not predict toxicity, with the exception of liver toxicity and neutropaenia. A high AUC(HD-MTX) was associated with better event-free survival (EFS) (P = 0.01) and overall survival (OAS) (P = 0.02). Both the AUC(HD-MTX) and the IELSG score were significant predictors of EFS and OAS in the adjusted model, with a hazard ratio of 0.82 and 0.73, respectively, per 100 mu mol l(-1) h(-1) increase in AUC(HD-MTX). CONCLUSIONS: Individualised dosing of HD-MTX might have the potential to improve clinical outcome in patients with PCNSL, even when administered concurrently with HD-AraC. In the future, this could be carried out by using first-cycle PK modelling with determination of potential dose adaptations for later cycles using Bayesian analysis. British Journal of Cancer (2010) 102, 673-677. doi:10.1038/sj.bjc.6605559 www.bjcancer.com Published online 2 February 2010 (C) 2010 Cancer Research UK
引用
收藏
页码:673 / 677
页数:5
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