Literature DB >> 32856157

Mycophenolic acid area under the concentration-time curve is associated with therapeutic response in childhood-onset lupus nephritis.

Astrid Godron-Dubrasquet1, Jean-Baptiste Woillard2,3, Stéphane Decramer4, Marc Fila5, Vincent Guigonis6, Stéphanie Tellier4, Denis Morin5, Maud Sordet1, Frank Saint-Marcoux2,3, Jérôme Harambat7,8.   

Abstract

BACKGROUND: Mycophenolic acid (MPA), the active compound of mycophenolate mofetil (MMF), is widely used in lupus nephritis treatment. Therapeutic drug monitoring of adults suggests that area under the concentration-time curve (AUC) of MPA (MPA-AUC) is associated with clinical outcomes, but childhood data are scarce.
METHODS: Retrospective study of 27 children with biopsy-proven lupus nephritis treated with MMF between 2008 and 2016. In 25 children, MPA-AUC was performed within 6 months after kidney biopsy and MMF initiation. Treatment response at 6 months was defined as normal or improved GFR by 25% compared with baseline, 50% reduction of proteinuria to < 0.5 g/day or 50 mg/mmol, and no hematuria.
RESULTS: A total of 62 MPA-AUC were analyzed in 27 patients. Overall median was 44 mg h/L (interquartile range [IQR] 33-54). Individual dose adaptation was required in 32 cases (52%) to achieve target AUC of 30-60 mg h/L. At 6 months, 14/25 patients were defined as responders (56%, median MPA-AUC 49 mg h/L (40-59)) and 11/25 as non-responders (44%, 29 mg h/L (24-38)). Patients with MPA-AUC levels > 45, 30-45, and < 30 mg h/L had 6-month response rates of 89% (8/9), 60% (6/10), and 0% (0/6), respectively. In a logistic regression model adjusted for age, sex, lupus nephritis classification, and time since MMF initiation, an MPA-AUC > 45 mg h/L was significantly associated with therapeutic response (OR 3.6, 95% CI 2.4-9.5, p = 0.03).
CONCLUSIONS: Therapeutic drug monitoring leading to individualized dosing may improve efficacy of MMF. MPA-AUC > 45 mg h/L is associated with better response rate and may be considered as a target value in pediatric lupus nephritis.

Entities:  

Keywords:  Children; Lupus nephritis; Mycophenolate mofetil; Therapeutic drug monitoring

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Year:  2020        PMID: 32856157     DOI: 10.1007/s00467-020-04733-x

Source DB:  PubMed          Journal:  Pediatr Nephrol        ISSN: 0931-041X            Impact factor:   3.714


  1 in total

1.  A national survey on current use of mycophenolate mofetil for childhood-onset systemic lupus erythematosus in Japan.

Authors:  Ryoki Hara; Hirotaka Miyazawa; Kenichi Nishimura; Takahiro Momoi; Tomo Nozawa; Masako Kikuchi; Nodoka Sakurai; Toshitaka Kizawa; Sanae Shimamura; Shinsuke Yasuda; Keiju Hiromura; Ken-ei Sada; Yasushi Kawaguchi; Naoto Tamura; Syuji Takei; Yoshinari Takasaki; Tatsuya Atsumi; Masaaki Mori
Journal:  Mod Rheumatol       Date:  2015-09-07       Impact factor: 3.023

  1 in total
  3 in total

1.  Pharmacokinetics of mycophenolic acid and external evaluation of two limited sampling strategies of drug exposure in patients with juvenile systematic lupus erythematosus.

Authors:  Quentin Beaulieu; Daolun Zhang; Isabelle Melki; Véronique Baudouin; Lauriane Goldwirst; Jean-Baptiste Woillard; Evelyne Jacqz-Aigrain
Journal:  Eur J Clin Pharmacol       Date:  2022-03-16       Impact factor: 2.953

2.  PK/PD Study of Mycophenolate Mofetil in Children With Systemic Lupus Erythematosus to Inform Model-Based Precision Dosing.

Authors:  Yewei Chen; Li Sun; Hong Xu; Min Dong; Tomoyuki Mizuno; Alexander A Vinks; Hermine I Brunner; Yifan Li; Zhiping Li
Journal:  Front Pharmacol       Date:  2020-12-21       Impact factor: 5.810

Review 3.  Recent Advances in Therapeutic Drug Monitoring of Voriconazole, Mycophenolic Acid, and Vancomycin: A Literature Review of Pediatric Studies.

Authors:  Matylda Resztak; Joanna Sobiak; Andrzej Czyrski
Journal:  Pharmaceutics       Date:  2021-11-23       Impact factor: 6.321

  3 in total

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