TY - JOUR
T1 - Erythrocyte concentrations of metabolites or cumulative doses of 6-mercaptopurine and methotrexate do not predict liver changes in children treated for acute lymphoblastic leukemia
AU - Halonen, Päivi
AU - Mattila, Jorma
AU - Mäkipernaa, Anne
AU - Ruuska, Tarja
AU - Schmiegelow, Kjeld
N1 - (c) 2006 Wiley-Liss, Inc.
PY - 2006/6
Y1 - 2006/6
N2 - BACKGROUND: During therapy consisting of 6MP and MTX, metabolites accumulate in the erythrocytes. The erythrocyte levels of metabolites reflect the intensity of therapy. Whether they are associated with hepatotoxicity manifested as histological liver changes is not known. We studied the association of the metabolites and cumulative doses of 6MP and MTX with histological liver disease.METHODS: Serial measurements of E-TGN, E-MTX, and ALT during maintenance therapy were performed and cumulative doses of 6MP and MTX were calculated as g/m2 in 16 children with ALL. Each subject underwent a percutaneous liver biopsy at the end of therapy to screen for histological liver disease.RESULTS: No differences in E-TGN, E-MTX, or cumulative doses of 6MP or MTX were detected in the children with ALL with liver fibrosis compared to those without fibrosis, or in the children with less liver fatty change compared to those with more fatty change. Serum median ALT levels correlated significantly positively with cumulative doses of 6MP during therapy (rS = 0.527, P = 0.036), but not with cumulative doses of MTX, or E-TGN, or E-MTX.CONCLUSIONS: Erythrocyte levels of the metabolites or the cumulative doses of 6MP and MTX do not predict histological liver disease in children treated for ALL.
AB - BACKGROUND: During therapy consisting of 6MP and MTX, metabolites accumulate in the erythrocytes. The erythrocyte levels of metabolites reflect the intensity of therapy. Whether they are associated with hepatotoxicity manifested as histological liver changes is not known. We studied the association of the metabolites and cumulative doses of 6MP and MTX with histological liver disease.METHODS: Serial measurements of E-TGN, E-MTX, and ALT during maintenance therapy were performed and cumulative doses of 6MP and MTX were calculated as g/m2 in 16 children with ALL. Each subject underwent a percutaneous liver biopsy at the end of therapy to screen for histological liver disease.RESULTS: No differences in E-TGN, E-MTX, or cumulative doses of 6MP or MTX were detected in the children with ALL with liver fibrosis compared to those without fibrosis, or in the children with less liver fatty change compared to those with more fatty change. Serum median ALT levels correlated significantly positively with cumulative doses of 6MP during therapy (rS = 0.527, P = 0.036), but not with cumulative doses of MTX, or E-TGN, or E-MTX.CONCLUSIONS: Erythrocyte levels of the metabolites or the cumulative doses of 6MP and MTX do not predict histological liver disease in children treated for ALL.
KW - Adolescent
KW - Antimetabolites, Antineoplastic/adverse effects
KW - Biomarkers/blood
KW - Chemical and Drug Induced Liver Injury/blood
KW - Child
KW - Child, Preschool
KW - Dose-Response Relationship, Drug
KW - Drug Monitoring
KW - Erythrocytes/metabolism
KW - Female
KW - Humans
KW - Liver Cirrhosis/blood
KW - Male
KW - Mercaptopurine/adverse effects
KW - Methotrexate/adverse effects
KW - Precursor Cell Lymphoblastic Leukemia-Lymphoma/complications
KW - Statistics, Nonparametric
U2 - 10.1002/pbc.20442
DO - 10.1002/pbc.20442
M3 - Journal article
C2 - 16395677
SN - 1545-5009
VL - 46
SP - 762
EP - 766
JO - Pediatric Blood & Cancer
JF - Pediatric Blood & Cancer
IS - 7
ER -