Abstract
Aim:
To evaluate the pharmacokinetics of tacrolimus in Chinese stable liver transplant recipients converted from immediate release (IR) tacrolimus-based immunosuppression to modified release (MR) tacrolimus-based immunosuppression.
Methods:
Open-label, multi-center study with a one-way conversion design was conducted. Eighty-three stable liver recipients (6–24 months post-transplant) with normal renal and stable hepatic function were converted from IR tacrolimus twice-daily treatment to MR tacrolimus once-daily treatment on a 1:1 (mg: mg) total daily dose basis. Twenty-four hour pharmacokinetic studies were carried out on d 0 (pre-conversion), d 1, and d 84 (post-conversion).
Results:
The area under the blood concentration–time curve of MR tacrolimus from 0 to 24 h (AUC0–24) on d 1 was comparable to that of IR tacrolimus on d 0, with a 90% confidence interval (CI) for MR/IR tacrolimus of 92%–97%. The AUC0–24 value for MR tacrolimus on d 84 with the daily dose increased by 14% was approximately 17% lower than that for IR tacrolimus. The 90% CI was 77%–90%, outside the bioequivalence range of 80%–125%. There was a good correlation between AUC0–24 and concentration at 24 h (C24) for IR tacrolimus (d 0, r=0.930) and MR tacrolimus (d 1, r=0.936; d 84, r=0.903).
Conclusion:
The exposure to tacrolimus when administered MR tacrolimus once daily is not equivalent to that for IR tacrolimus twice daily after an 84-day conversion in Chinese stable liver transplant recipients. The dose should be adjusted on the basis of trough levels. The therapeutic drug monitoring for patients treated with IR tacrolimus is considered to be applicable to MR tacrolimus.
Similar content being viewed by others
Log in or create a free account to read this content
Gain free access to this article, as well as selected content from this journal and more on nature.com
or
References
Staatz CE, Tett SE . Clinical pharmacokinetics and pharmacodynamics of tacrolimus in solid organ transplantation. Clin Pharmacokinet 2004; 43: 623–53.
Gewirtz AT, Sitaraman SV . Tacrolimus Fujisawa. Curr Opin Investig Drugs 2002; 3: 1307–11.
Scott L, McKeage K, Keam SJ, Plosker GL . Tacrolimus: a further update of its use in the management of organ transplantation. Drugs 2003; 63: 1247–97.
Wallemacq P, Armstrong VW, Brunet M, Haufroid V, Holt DW, Johnston A, et al. Opportunities to optimize tacrolimus therapy in solid organ transplantation: report of the European consensus conference. Ther Drug Monit 2009; 31: 139–52.
First MR, Fitzsimmons WE . Modified release tacrolimus. Yonsei Med J 2004; 45: 1127–31.
Wente MN, Sauer P, Mehrabi A, Weitz J, Büchler MW, Schmidt J, et al. Review of the clinical experience with a modified release form of tacrolimus [FK506E (MR4)] in transplantation. Clin Transplant 2006; 20 Suppl 17: 80–4.
Chisholm MA, Middleton MD . Modified-release tacrolimus. Ann Pharmacother 2006; 40: 270–5.
First MR . First clinical experience with the new once-daily formulation of tacrolimus. Ther Drug Monit 2008; 30: 159–66.
Florman S, Alloway R, Kalayoglu M, Lake K, Bak T, Klain A, et al. Conversion of stable liver transplant recipients from a twice-daily Prograf-based regimen to a once-daily modified release tacrolimus-based regimen. Transplant Proc 2005; 37: 1211–3.
Alloway R, Steinberg S, Khalil K, Gourishankar S, Miller J, Norman D, et al. Conversion of stable kidney transplant recipients from a twice-daily Prograf-based regimen to a once-daily modified release tacrolimus-based regimen. Transplant Proc 2005; 37: 867–70.
Alloway R, Vanhaecke J, Yonan N, White M, Haddad H, Rábago G et al. Pharmacokinetics in stable heart transplant recipients after conversion from twice-daily to once-daily tacrolimus formulations. J Heart Lung Transplant Epub 2011; 30: 1003–10.
Wlodarczyk Z, Squifflet JP, Ostrowski M, Rigotti P, Stefoni S, Citterio F, et al. Pharmacokinetics for once- versus twice-daily tacrolimus formulations in de novo kidney transplantation: a randomized, open-label trial. Am J Transplant 2009; 9: 2505–13.
Fischer L, Trunecka P, Gridelli B, Roy A, Vitale A, Vajdivieso A, et al. Pharmacokinetics for once-daily versus twice-daily tacrolimus formulations in de novo liver transplantation: a randomized, open label trial. Liver Transplantation 2011; 17: 167–77.
Zhang YF, Chen XY, Dai XJ, Ao JH, Zhong DF . Comparison of pharmacokinetics of tacrolimus in Chinese de novo kidney transplant patients after repeated-dose of modified release tacrolimus and immediate release tacrolimus. Chin J Clin Pharmacol 2011; 27: In press. Chinese.
Merli M, Di Menna S, Giusto M, Giannelli V, Lucidi C, Loria S, et al. Conversion from twice-daily to once-daily tacrolimus administration in liver transplant patient. Transplant Proc 2010; 42: 1322–4.
Hougardy JM, Broeders N, Kianda M, Massart A, Madhoun P, Le Moine A, et al. Conversion from Prograf to Advagraf among kidney transplant recipients results in sustained decrease in tacrolimus exposure. Transplantation 2011; 91: 566–9.
Marzoa-Rivas R, Paniagua-Martín MJ, Barge-Caballero E, Pedrosa del Moral V, Barge-Caballero G, Grille-Cancela Z, et al. Conversion of heart transplant patients from standard to sustained-release tacrolimus requires a dosage increase. Transplant Proc 2010; 42: 2994–6.
Li GM, Zheng SS, Liu YF, Zhu ZJ, Xia Q, Zhou J, et al. A randomized trial on the efficacy and safety of Advagraf vs tacrolimus in prevention of acute liver allograft rejection. Chin J Organ Transplant 2011; 32: 217–20.
Acknowledgements
We would like to acknowledge Prof Shu-sen ZHENG of the First Affiliated Hospital, Zhejiang University; Prof Yong-feng LIU of the First Hospital of China Medical University; Prof Zhi-jun ZHU of Tianjin First Center Hospital; Prof Qiang XIA of Renji Hospital affiliated to Shanghai Jiao Tong University; Prof Jia FAN of Zhongshan Hospital Fudan University; and Prof Zhi-ren FU of Shanghai Changzheng Hospital for their assistance in performing the clinical studies.
Author information
Authors and Affiliations
Corresponding author
Rights and permissions
About this article
Cite this article
Zhang, Yf., Chen, Xy., Dai, Xj. et al. Pharmacokinetics of tacrolimus converted from twice-daily formulation to once-daily formulation in Chinese stable liver transplant recipients. Acta Pharmacol Sin 32, 1419–1423 (2011). https://doi.org/10.1038/aps.2011.125
Received:
Accepted:
Published:
Issue date:
DOI: https://doi.org/10.1038/aps.2011.125
Keywords
This article is cited by
-
Clinical Pharmacokinetics of Once-Daily Tacrolimus in Solid-Organ Transplant Patients
Clinical Pharmacokinetics (2015)


