A prospective cohort conversion study of twice-daily to once-daily extended-release tacrolimus: role of ethnicity

被引:11
|
作者
Glick, Lauren [1 ]
Shamy, Fernanda [2 ]
Nash, Michelle [2 ]
Sokwala, Ahmed [3 ]
Malavade, Tushar [3 ]
Prasad, G. V. Ramesh [4 ]
Zaltzman, Jeffrey S. [4 ]
机构
[1] St Michaels, Keenan Summer Student Res Program, Toronto, ON M5B21W8, Canada
[2] St Michaels, Transplant Program, Toronto, ON M5B 1W8, Canada
[3] Univ Toronto, St Michaels, Nephrol Training Program, Toronto, ON M5B 1W8, Canada
[4] St Michaels, Div Nephrol, Dept Med, Keenan Res Inst, 30 Bond St, Toronto, ON M5B 1W8, Canada
来源
关键词
D O I
10.1186/2047-1440-3-7
中图分类号
R3 [基础医学]; R4 [临床医学];
学科分类号
1001 ; 1002 ; 100602 ;
摘要
Background: Tacrolimus is a widely used calcineurin inhibitor in kidney transplantation. It is available as twice-daily Prograf (R) (Tac-BID) and once-daily Advagraf (R) (Tac-OD). Although therapeutically equivalent, some patients require dose adjustments to achieve similar trough concentrations [C-0] after conversion. Tacrolimus exposure is affected by ethnicity in the de novo setting but the role of ethnicity in determining dose requirements and adjustments after conversion is unknown. Methods: In this study, 496 renal transplant recipients (RTRs) were prospectively converted from Tac-BID to Tac-OD, with dose adjustments targeted to achieve similar [C-0] at 12 months post-conversion. Renal function, acute rejection and Tac dose adjustments by ethnicity were analyzed. Results: There were similar numbers of recipients from living and deceased donors. The mean transplant duration was 7 years. Of the RTRs, 60% were Caucasian and 40% were identified as belonging to an ethnic minority. There was no change in estimated renal function (eGFR) post-conversion to Tac-OD. At 12 months, 35/488 (7%) RTRs were receiving a reduced dose, 101/488 (21%) required a dose increase of which 77 (16%) were receiving at least a 30% increase in dose over baseline. The percentage of those in ethnic groups requiring a dose increase of >30% varied from 8.0% for South Asians to 27.5% for East Asians (P = 0.03), despite East Asians having a similar baseline dose of Tac-BID (3.59 mg/day) compared to the entire cohort (3.53 mg/day). Conclusions: Ethnicity may play an important role in dosing requirements when converting from Tac-BID to Tac-OD, unrelated to baseline dose. Further investigation is required to determine the reasons for ethnic variability when patients are converted between tacrolimus preparations.
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