Randomized Trial of Ciclosporin with 2-h Monitoring vs. Tacrolimus with Trough Monitoring in Liver Transplantation: DELTA Study

被引:1
|
作者
Ruijter, Bastian N. [1 ]
Inderson, Akin [1 ]
van den Berg, Aad P. [2 ]
Metselaar, Herold J. [3 ]
Dubbeld, Jeroen [4 ]
Tushuizen, Maarten E. [1 ]
Porte, Robert J. [5 ]
Polak, Wojciech [6 ]
van der Helm, Danny [1 ]
van Reeven, Marjolein [6 ]
Rodriguez-Girondo, Mar [7 ]
van Hoek, Bart [1 ,8 ]
机构
[1] Leiden Univ, LUMC Transplantat Ctr, Dept Gastroenterol & Hepatol, Med Ctr, Leiden, Netherlands
[2] Univ Med Ctr Groningen, Dept Gastroenterol & Hepatol, Groningen, Netherlands
[3] Erasmus MC, Erasmus MC Transplant Inst, Dept Gastroenterol & Hepatol, Rotterdam, Netherlands
[4] Leiden Univ, LUMC Transplantat Ctr, Dept Surg, Med Ctr, Leiden, Netherlands
[5] Univ Groningen, Univ Med Ctr Groningen, Dept Surg, Sect HPB Surg & Liver Transplantat, Groningen, Netherlands
[6] Erasmus MC, Erasmus MC Transplant Inst, Dept Surg, Div HPB & Transplant Surg, Rotterdam, Netherlands
[7] Leiden Univ, Dept Biomed Data Sci, Med Ctr, Leiden, Netherlands
[8] Leiden Univ, Med Ctr, Dept Gastroenterol & Hepatol, Hepatol, Albinusdreef 2,POB 9600,C4-P, NL-2300 RC Leiden, Netherlands
关键词
Adverse effects; Ciclosporin; Liver transplantation; Outcome; Ran-domized controlled trial; Rejection; Survival; Renal function; Tacrolimus; FOLLOW-UP; MYCOPHENOLATE-MOFETIL; MICROEMULSIFIED CYCLOSPORINE; RECIPIENTS; EFFICACY; IMMUNOSUPPRESSION; TOLERABILITY; MULTICENTER; SAFETY; MODEL;
D O I
10.14218/JCTH.2022.00348
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background and Aims: Previous trials comparing cyclo-sporine and tacrolimus after liver transplantation (LT) showed conflicting results. Most used trough monitoring for cyclo-sporine (C0), leading to less accurate dosing than with 2-h monitoring (C2). Only one larger trial compared C2 with tac-rolimus based on trough level (T0) after LT, with similar treat-ed biopsy-proven acute rejection (tBPAR) and graft loss, while a smaller trial had less tBPAR with C2 compared to T0. There-fore, it is still unclear which calcineurin inhibitor is preferred after LT. We aimed to demonstrate superior efficacy (tBPAR), tolerability, and safety of C2 or T0 after first LT. Methods: Patients after first LT were randomized to C2 or T0. tBPAR, patient-and graft survival, safety and tolerability were the main endpoints, with analysis by Fisher test, Kaplan-Meier survival analysis and log-rank test. Results: In intention-to- treat analysis 84 patients on C2 and 85 on T0 were included. Cumulative incidence of tBPAR C2 vs. T0 was 17.7% vs. 8.4% at 3 months (p=0.104), and 21.9% vs. 9.7% at 6 and 12 months (p=0.049). One-year cumulative mortality C2 vs. T0 was 15.5% vs. 5.9% (p=0.049) and graft loss 23.8% vs. 9.4% (p=0.015). Serum triglyceride and LDL-cholesterol was lower with T0 than with C2. Incidence of diarrhea in T0 vs, C2 was 64% vs. 31% (p <= 0.001), with no other differences in safety and tolerability. Conclusions: In the first year after LT immunosuppression with T0 leads to less tBPAR and better patient-/re-transplant-free survival as compared to C2.
引用
收藏
页码:839 / 849
页数:11
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