Literature DB >> 19132729

Pharmacokinetics of high-dose methotrexate in infants treated for acute lymphoblastic leukemia.

Gudmar Lönnerholm1, Maria Grazia Valsecchi, Paola De Lorenzo, Martin Schrappe, Liisa Hovi, Myriam Campbell, Georg Mann, Gritta Janka-Schaub, Chi-Kong Li, Jan Stary, Ian Hann, Rob Pieters.   

Abstract

BACKGROUND: Interfant-99 was an international collaborative treatment protocol for infants with acute lymphoblastic leukemia (ALL). PROCEDURE: We collected data on 103 infants at the time of their first treatment with high-dose methotrexate (HD MTX), 5 g/m(2). Children <6 months of age received two-third of the calculated dose based on body surface area (BSA), children 6-12 months three-fourth of the calculated dose, and children >12 months full dose.
RESULTS: The median steady-state MTX concentration at the end of the 24-hr infusion was 57.8 microM (range 9.5-313). The median systemic clearance was 6.22 L/hr/m(2) BSA, and tended to increase with age (P = 0.099). Boys had higher clearance than girls, 6.77 and 5.28 L/hr/m(2) (P = 0.030), and tended to have lower median MTX concentration at 24 hr. Eight infants had MTX levels below 20 microM, a level judged to be sufficient in B-lineage ALL in children >1 year of age. All infants tolerated the dose well enough to receive a second dose of HD MTX without dose reduction. We found no significant effect on disease-free survival for MTX steady-state concentration, MTX clearance, or time to MTX below 0.2 microM.
CONCLUSIONS: Our data provide no support for a change in the dosing rules for MTX used in Interfant-99. However, in view of the poor treatment results for infants, one might consider increase in the dose for patients who reach plasma levels below median after the first MTX dose. (c) 2009 Wiley-Liss, Inc.

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Year:  2009        PMID: 19132729     DOI: 10.1002/pbc.21925

Source DB:  PubMed          Journal:  Pediatr Blood Cancer        ISSN: 1545-5009            Impact factor:   3.167


  6 in total

1.  Interspecies scaling for the prediction of drug clearance in children: application of maximum lifespan potential and an empirical correction factor.

Authors:  Iftekhar Mahmood
Journal:  Clin Pharmacokinet       Date:  2010-07       Impact factor: 6.447

2.  The Population Pharmacokinetics of High-Dose Methotrexate in Infants with Acute Lymphoblastic Leukemia Highlight the Need for Bedside Individualized Dose Adjustment: A Report from the Children's Oncology Group.

Authors:  Ryan J Beechinor; Patrick A Thompson; Michael F Hwang; Ryan C Vargo; Lisa R Bomgaars; Jacqueline G Gerhart; ZoAnn E Dreyer; Daniel Gonzalez
Journal:  Clin Pharmacokinet       Date:  2019-07       Impact factor: 6.447

Review 3.  Infant acute lymphoblastic leukemia: Lessons learned and future directions.

Authors:  Rob Pieters
Journal:  Curr Hematol Malig Rep       Date:  2009-07       Impact factor: 3.952

4.  Pharmacokinetic basis for dosing high-dose methotrexate in infants and young children with malignant brain tumours.

Authors:  John C Panetta; Jessica K Roberts; Jie Huang; Tong Lin; Vinay M Daryani; K Elaine Harstead; Yogesh T Patel; Arzu Onar-Thomas; Olivia Campagne; Deborah A Ward; Alberto Broniscer; Giles Robinson; Amar Gajjar; Clinton F Stewart
Journal:  Br J Clin Pharmacol       Date:  2020-01-08       Impact factor: 4.335

5.  Effect of the Polymorphism of Folylpolyglutamate Synthetase on Treatment of High-Dose Methotrexate in Pediatric Patients with Acute Lymphocytic Leukemia.

Authors:  Zhen Huang; Hong-Fei Tong; Yuan Li; Jiang-Chao Qian; Ju-Xiang Wang; Zhe Wang; Ji-Chen Ruan
Journal:  Med Sci Monit       Date:  2016-12-17

6.  LC-MS metabolomics comparisons of cancer cell and macrophage responses to methotrexate and polymer-encapsulated methotrexate.

Authors:  Mohammad Ahmad Al-Natour; Ali Alazzo; Amir M Ghaemmaghami; Dong-Hyun Kim; Cameron Alexander
Journal:  Int J Pharm X       Date:  2019-11-12
  6 in total

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