Pharmacokinetics of Mycophenolic Acid Administered 3 Times Daily after Hematopoietic Stem Cell Transplantation with Reduced-Intensity Regimen

Mycophenolate mofetil (MMF) is an immunosuppressive drug used as a prophylactic agent to prevent acute graft-versus-host disease (aGVHD) after hematopoietic stem cell transplantation (HSCT). After reduced-intensity conditioning (RIC) regimen, administration of MMF orally 3 times a day (tid) seems to...

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Veröffentlicht in:Biology of blood and marrow transplantation 2009-09, Vol.15 (9), p.1134-1139
Hauptverfasser: Royer, Bernard, Larosa, Fabrice, Legrand, Faezeh, Gerritsen-van Schieveen, Pauline, Bérard, Michel, Kantelip, Jean-Pierre, Deconinck, Eric
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Sprache:eng
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Zusammenfassung:Mycophenolate mofetil (MMF) is an immunosuppressive drug used as a prophylactic agent to prevent acute graft-versus-host disease (aGVHD) after hematopoietic stem cell transplantation (HSCT). After reduced-intensity conditioning (RIC) regimen, administration of MMF orally 3 times a day (tid) seems to be more beneficial than twice a day (bid). However, information regarding the pharmacokinetic (PK) parameters of mycophenolic acid (MPA), the active metabolite of MMF, administered in this regimen are very limited. We performed a prospective study in 15 patients for whom 3 sets of sampling were performed: at the beginning of the treatment, after 1 week, and after 1 month. Two consecutive 8-hour sets of sampling were performed at day 0 (D0) and D7. Plasma concentrations of MPA were quantified and areas under the curve for 8 hours (AUC0-8 ), and maximal and through concentrations were calculated. The results show that AUC0-8 increases between the beginning of treatment and the end of the first week, but remains stable thereafter. Moreover, a trend to lower AUC0-8 was observed for the patients who experienced GVHD ≥2 compared to those patients who did not. The other PK parameters are not associated with pharmacodynamic events. A limited sampling strategy with Bayesian estimators is currently under investigation to confirm these data and the role of D7 AUC0-8 as a potential target of therapeutic drug monitoring (TDM).
ISSN:1083-8791
1523-6536
DOI:10.1016/j.bbmt.2009.04.011