Renal Function in De Novo Liver Transplant Recipients Receiving Different Prolonged-Release Tacrolimus Regimens-The DIAMOND Study
Language English Country United States Media print-electronic
Document type Clinical Trial, Phase III, Journal Article, Multicenter Study, Randomized Controlled Trial
PubMed
25707487
PubMed Central
PMC5024030
DOI
10.1111/ajt.13182
PII: S1600-6135(22)00292-1
Knihovny.cz E-resources
- Keywords
- calcineurin inhibitor, clinical research/practice, clinical trial, glomerular filtration rate (GFR), immunosuppressant, immunosuppression/immune modulation, liver allograft function/dysfunction, liver transplantation/hepatology, liver transplantation: split, tacrolimus,
- MeSH
- Glomerular Filtration Rate MeSH
- Immunosuppressive Agents therapeutic use MeSH
- Liver physiology MeSH
- Middle Aged MeSH
- Humans MeSH
- Follow-Up Studies MeSH
- Liver Diseases physiopathology surgery MeSH
- Postoperative Complications MeSH
- Graft Survival physiology MeSH
- Prognosis MeSH
- Graft Rejection drug therapy pathology MeSH
- Risk Factors MeSH
- Tacrolimus therapeutic use MeSH
- Liver Transplantation * MeSH
- Kidney Function Tests MeSH
- Check Tag
- Middle Aged MeSH
- Humans MeSH
- Male MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
- Clinical Trial, Phase III MeSH
- Multicenter Study MeSH
- Randomized Controlled Trial MeSH
- Names of Substances
- Immunosuppressive Agents MeSH
- Tacrolimus MeSH
UNLABELLED: DIAMOND: multicenter, 24-week, randomized trial investigating the effect of different once-daily, prolonged-release tacrolimus dosing regimens on renal function after de novo liver transplantation. Arm 1: prolonged-release tacrolimus (initial dose 0.2mg/kg/day); Arm 2: prolonged-release tacrolimus (0.15-0.175mg/kg/day) plus basiliximab; Arm 3: prolonged-release tacrolimus (0.2mg/kg/day delayed until Day 5) plus basiliximab. All patients received MMF plus a bolus of corticosteroid (no maintenance steroids). PRIMARY ENDPOINT: eGFR (MDRD4) at Week 24. Secondary endpoints: composite efficacy failure, BCAR and AEs. Baseline characteristics were comparable. Tacrolimus trough levels were readily achieved posttransplant; initially lower in Arm 2 versus 1 with delayed initiation in Arm 3. eGFR (MDRD4) was higher in Arms 2 and 3 versus 1 (p = 0.001, p = 0.047). Kaplan-Meier estimates of composite efficacy failure-free survival were 72.0%, 77.6%, 73.9% in Arms 1-3. BCAR incidence was significantly lower in Arm 2 versus 1 and 3 (p = 0.016, p = 0.039). AEs were comparable. Prolonged-release tacrolimus (0.15-0.175mg/kg/day) immediately posttransplant plus basiliximab and MMF (without maintenance corticosteroids) was associated with lower tacrolimus exposure, and significantly reduced renal function impairment and BCAR incidence versus prolonged-release tacrolimus (0.2mg/kg/day) administered immediately posttransplant. Delayed higher-dose prolonged-release tacrolimus initiation significantly reduced renal function impairment compared with immediate posttransplant administration, but BCAR incidence was comparable.
Abdominal Transplant Surgery University Hospitals Leuven Leuven Belgium
Astellas Pharma Europe Ltd London United Kingdom
Astellas Pharma Inc Northbrook IL
Department of Abdominal Surgery A 5 Vishnevsky Institute of Surgery Moscow Russian Federation
Department of General Visceral and Transplantation Surgery Hannover Medical School Hannover Germany
Department of General Visceral and Vascular Surgery Jena University Hospital Thuringia Germany
Department of Nephrology and Organ Transplantation Toulouse University Hospital Toulouse France
Department of Surgery Goethe University Hospital and Clinics Frankfurt Germany
Department of Transplantation and Liver Surgery Clinic Helsinki University Hospital Helsinki Finland
Liver Transplant Unit Policlinico di Tor Vergata Rome Italy
The Transplant Institute Sahlgrenska University Hospital Gothenburg Sweden
Transplantcentre Institute for Clinical and Experimental Medicine Prague Czech Republic
See more in PubMed
Neuberger JM, Mamelok RD, Neuhaus P, et al. Delayed introduction of reduced‐dose tacrolimus, and renal function in liver transplantation: The “ReSpECT” study. Am J Transplant 2009; 9: 327–336. PubMed
World Health Organization. Part 1: Definition, diagnosis and classification of diabetes mellitus and its complications. WHO/NCD/NCS/99.2 1999; Available at: http://whqlibdoc.who.int/hq/1999/who_ncd_ncs_99.2.pdf. Assessed November 2014.
Trunečka P, Boillot O, Seehofer D, et al. Once‐daily prolonged‐release tacrolimus (ADVAGRAF) versus twice‐daily tacrolimus (PROGRAF) in liver transplantation. Am J Transplant 2010; 10: 2313–2323. PubMed
Boudjema K, Camus C, Saliba F, et al. Reduced‐dose tacrolimus with mycophenolate mofetil vs standard‐dose tacrolimus in liver transplantation: A randomized study. Am J Transplant 2011; 11: 965–976. PubMed
Wu LW, Guo ZY, Tai Q, et al. Steroid elimination within 24 hours after orthotopic liver transplantation: Effectiveness and tolerability. Hepatobiliary Pancreat Dis Int 2012; 11: 137–142. PubMed
Bodziak KA, Hricik DE. New‐onset diabetes mellitus after solid organ transplantation. Transpl Int 2009; 22: 519–530. PubMed