TY - JOUR
T1 - COMBINATION OF EXTENDED-RELEASE TACROLIMUS PLUS EVEROLIMUS ONCE-DAILY IN DE NOVO KIDNEY TRANSPLANT RECIPIENTS: ER-TAC VERSUS LCPT
AU - Spagnoletti, Gionata
AU - Salerno, Maria Paola
AU - De Gennaro, Flavia
AU - Romagnoli, Jacopo
AU - Citterio, Franco
PY - 2019
Y1 - 2019
N2 - Introduction: Combination of Everolimus (EVR) with Tacrolimus (Tac) permits reduced calcineurin inhibitors exposure and, recently, has been demonstrated safe and effective.
Two different once-daily Tacrolimus formulations, with different pharmacokinetic profiles are now available: ER-Tac and LCPT. Aim of this study was to compare in kidney transplant recipients (KTx), the
short-term efficacy and safety of ER-Tac versus LCPT, both in combination with EVR, administered concomitantly once a day.
Methods: Fifty-seven KTx were openrandomized to once-daily maintenance immunosuppressive regimen based on ER-Tac + EVR + Steroids (ERTac + EVR, n = 30) or LCPT + EVR + Steroids (LCPT + EVR, n = 27). All patients received induction therapy with Thymoglobuline (total dose 200 mg).
Results: Median follow-up was 10 months (range 3–18). Here we present the intention-to-treat analysis at 6 months. There were no differences in patients as well as in graft survival. Moreover, we found no differences in renal function, acute rejection rate, CMV infection. According to the Concentration/Dose ratio of Tacrolimus, there was a significantly higher number of slow metabolizers 1-month after transplant in the LCPT + EVR group. Data are detailed below (Table 1).
Conclusions: Our data show that the two extended release Tac formulations, when administered with EVR once-daily, have comparable 6-month safety and efficacy. We can speculate that the higher number of slow metabolizers in the LCPT group may be an advantage to reach target exposure early after transplantation.
AB - Introduction: Combination of Everolimus (EVR) with Tacrolimus (Tac) permits reduced calcineurin inhibitors exposure and, recently, has been demonstrated safe and effective.
Two different once-daily Tacrolimus formulations, with different pharmacokinetic profiles are now available: ER-Tac and LCPT. Aim of this study was to compare in kidney transplant recipients (KTx), the
short-term efficacy and safety of ER-Tac versus LCPT, both in combination with EVR, administered concomitantly once a day.
Methods: Fifty-seven KTx were openrandomized to once-daily maintenance immunosuppressive regimen based on ER-Tac + EVR + Steroids (ERTac + EVR, n = 30) or LCPT + EVR + Steroids (LCPT + EVR, n = 27). All patients received induction therapy with Thymoglobuline (total dose 200 mg).
Results: Median follow-up was 10 months (range 3–18). Here we present the intention-to-treat analysis at 6 months. There were no differences in patients as well as in graft survival. Moreover, we found no differences in renal function, acute rejection rate, CMV infection. According to the Concentration/Dose ratio of Tacrolimus, there was a significantly higher number of slow metabolizers 1-month after transplant in the LCPT + EVR group. Data are detailed below (Table 1).
Conclusions: Our data show that the two extended release Tac formulations, when administered with EVR once-daily, have comparable 6-month safety and efficacy. We can speculate that the higher number of slow metabolizers in the LCPT group may be an advantage to reach target exposure early after transplantation.
KW - kidney transplant
KW - kidney transplant
UR - http://hdl.handle.net/10807/159661
M3 - Meeting Abstract
SN - 0934-0874
VL - 32
SP - 140
EP - 140
JO - Transplant International
JF - Transplant International
ER -