High methotrexate exposure and toxicity in children with t(9;22) positive acute lymphoblastic leukaemia treated with imatinib

被引:8
|
作者
Loue, C. [1 ]
Garnier, N. [1 ]
Bertrand, Y. [1 ]
Bleyzac, N. [1 ,2 ]
机构
[1] IHOP, Pediat Hematol & Oncol Unit, Lyon 08, France
[2] Univ Lyon 1, UMR CNRS 5558, Lab Biometrie & Biol Evolut, F-69622 Villeurbanne, France
关键词
children; drug interaction; imatinib; methotrexate; CANCER; ABCG2; TRANSPORTERS; RESISTANCE; MESYLATE;
D O I
10.1111/jcpt.12298
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
What is known and objectiveAlthough there is one report on the possible reduced clearance of methotrexate in an adult patient when given concomitantly with imatinib, there is little information on the possible pharmacokinetic interaction. Wereport on three cases of delayed elimination of methotrexate in children with chromosome Philadelphia-positive acute lymphoblastic leukaemia treated concomitantly with imatinib. Case summaryThree patients, aged 9-17years, presented with high methotrexate blood levels following co-administration of imatinib and high-dose methotrexate. Two patients presented with clinical symptoms (nausea, epigastric pain and mucositis, acute renal failure, liver cytolysis). One patient required extrasupplementary folinic acid doses than used in the standard protocol and one child required the use of carboxypeptidase-G2. What is new and conclusionThere is an apparent pharmacokinetic interaction between imatinib and methotrexate in children. Several mechanisms could explain this interaction, including competition for BCRP or ABCB transporters. Temporary withdrawal of imatinib may be necessary for preventing severe methotrexate-related adverse events.
引用
收藏
页码:599 / 600
页数:2
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