Literature DB >> 12721759

High-dose methotrexate: on the relationship of methotrexate elimination time vs renal function and serum methotrexate levels in 1164 courses in 264 Swedish children with acute lymphoblastic leukaemia (ALL).

T Skärby1, P Jönsson, L Hjorth, M Behrentz, O Björk, E Forestier, M Jarfelt, G Lönnerholm, P Höglund.   

Abstract

PURPOSE: The objectives of the present study were to determine the relationship between methotrexate (MTX) elimination time and various aspects of renal function and to evaluate the prognostic value of elevated serum MTX and creatinine for delayed MTX elimination. PATIENTS AND METHODS: The majority of the 264 children were being treated for ALL. According to the NOPHO-92 protocol, 5 or 8 g MTX/m(2) was administered over 24 h. Serum creatinine was assessed daily. In 11 patients from one centre, renal function was studied in more detail using serum cystatin C, iohexol clearance, and urinary albumin, IgG and protein HC.
RESULTS: Increased serum creatinine correlated significantly with the elimination time of MTX, whereas no indications were found of tubular or barrier function damage. Of the 1164 courses, 44 had delayed elimination of MTX (>/=120 h). Serum MTX >150 microM at the end of infusion had a sensitivity of 0.27 and a specificity of 0.94 to predict delayed MTX elimination, and >/=50% increase in serum creatinine during the first treatment day (creatinine ratio) had a sensitivity of 0.32 and a specificity of 0.99. The corresponding risk ratios were 5 and 19 for MTX >150 micro M and creatinine ratio, respectively. In courses with a normal elimination time (<72 h), 99% of the courses had a rise in serum creatinine of less than 50%.
CONCLUSIONS: Elevation of serum creatinine by more than 50% is a better predictor of delayed elimination than the level of serum MTX at the end of MTX infusion, especially if information on previous creatinine measurements is used to reduce the impact of an occasionally low serum creatinine value before the start of the MTX infusion.

Entities:  

Mesh:

Substances:

Year:  2003        PMID: 12721759     DOI: 10.1007/s00280-002-0552-1

Source DB:  PubMed          Journal:  Cancer Chemother Pharmacol        ISSN: 0344-5704            Impact factor:   3.333


  16 in total

1.  Population pharmacokinetics of high-dose methotrexate in children with acute lymphoblastic leukaemia.

Authors:  Dolores Aumente; Dolores Santos Buelga; John C Lukas; Pedro Gomez; Antonio Torres; Maria José García
Journal:  Clin Pharmacokinet       Date:  2006       Impact factor: 6.447

2.  Case files of the New York City Poison Control Center: antidotal strategies for the management of methotrexate toxicity.

Authors:  Silas W Smith; Lewis S Nelson
Journal:  J Med Toxicol       Date:  2008-06

Review 3.  Clinical pharmacology in the adolescent oncology patient.

Authors:  Gareth J Veal; Christine M Hartford; Clinton F Stewart
Journal:  J Clin Oncol       Date:  2010-05-03       Impact factor: 44.544

4.  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

5.  Challenges in implementing individualized medicine illustrated by antimetabolite therapy of childhood acute lymphoblastic leukemia.

Authors:  Jacob Nersting; Louise Borst; Kjeld Schmiegelow
Journal:  Clin Proteomics       Date:  2011-06-03       Impact factor: 3.988

6.  A Systematic Review of Population Pharmacokinetic Models of Methotrexate.

Authors:  Yiming Zhang; Liyu Sun; Xinwei Chen; Libo Zhao; Xiaoling Wang; Zhigang Zhao; Shenghui Mei
Journal:  Eur J Drug Metab Pharmacokinet       Date:  2022-01-05       Impact factor: 2.441

7.  Risk prediction for delayed clearance of high-dose methotrexate in pediatric hematological malignancies by machine learning.

Authors:  Min Zhan; Zebin Chen; Changcai Ding; Qiang Qu; Guoqiang Wang; Sixi Liu; Feiqiu Wen
Journal:  Int J Hematol       Date:  2021-06-25       Impact factor: 2.490

8.  Methotrexate Associated Renal Impairment Is Related to Delayed Elimination of High-Dose Methotrexate.

Authors:  Shi-Long Yang; Fen-Ying Zhao; Hua Song; Di-Ying Shen; Xiao-Jun Xu
Journal:  ScientificWorldJournal       Date:  2015-06-21

9.  Evaluation of body-surface-area adjusted dosing of high-dose methotrexate by population pharmacokinetics in a large cohort of cancer patients.

Authors:  Usman Arshad; Max Taubert; Tamina Seeger-Nukpezah; Sami Ullah; Kirsten C Spindeldreier; Ulrich Jaehde; Michael Hallek; Uwe Fuhr; Jörg Janne Vehreschild; Carolin Jakob
Journal:  BMC Cancer       Date:  2021-06-20       Impact factor: 4.430

10.  N-acetylcysteine renoprotection in methotrexate induced nephrotoxicity and its effects on B-cell lymphoma.

Authors:  Ruchi Singh; Rikin Shah; Curtis Turner; Osvaldo Regueira; Tetyana L Vasylyeva
Journal:  Indian J Med Paediatr Oncol       Date:  2015 Oct-Dec
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.