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Tacrolimus Once Daily (ADVAGRAF) Versus Twice Daily (PROGRAF) in De Novo Renal Transplantation: A Randomized Phase III Study
被引:139
|作者:
Kraemer, B. K.
[1
]
Charpentier, B.
[2
]
Backman, L.
[3
,4
]
Silva, H. Tedesco, Jr.
[5
]
Mondragon-Ramirez, G.
[6
]
Cassuto-Viguier, E.
[7
]
Mourad, G.
[8
]
Sola, R.
[9
]
Rigotti, P.
[10
]
Ortuno Mirete, J.
[11
]
机构:
[1] Univ Heidelberg, Med Klin 5, Univ Klinikum Mannheim, Mannheim, Germany
[2] Univ Paris Sud, Hop Bicetre, Villejuif, France
[3] Univ Uppsala Hosp, Uppsala, Sweden
[4] Sahlgrens Univ Hosp, Gothenburg, Sweden
[5] Univ Fed Sao Paulo, Fundacao Oswaldo Ramos, Sao Paulo, Brazil
[6] Inst Mexicano Transplantes, Cuernavaca, Morelos, Mexico
[7] Serv Nephrol, Nice, France
[8] Hop Lapeyronie, Montpellier, France
[9] Fundacio Puigvert, Barcelona, Spain
[10] Azienda Osped Padova, Padua, Italy
[11] Hosp Ramon & Cajal, E-28034 Madrid, Spain
关键词:
Biopsy-proven acute rejection;
immunosuppression;
kidney transplantation;
noninferiority study;
prolonged-release tacrolimus;
tacrolimus;
GLOMERULAR-FILTRATION-RATE;
KIDNEY-TRANSPLANTATION;
MYCOPHENOLATE-MOFETIL;
RECIPIENTS;
ADHERENCE;
IMMUNOSUPPRESSANTS;
FORMULATION;
THERAPY;
LIVER;
TRIAL;
D O I:
10.1111/j.1600-6143.2010.03256.x
中图分类号:
R61 [外科手术学];
学科分类号:
摘要:
This multicenter, 1:1-randomized, parallel-group, noninferiority study compared the efficacy and safety of twice-daily tacrolimus (Tacrolimus BID; Prograf) and once-daily tacrolimus prolonged release (Tacrolimus QD; Advagraf), combined with steroids and low-dose mycophenolate mofetil without antibody induction, in 667 de novo kidney transplant recipients. A double-blind, double-dummy 24-week period was followed by an open extension of up to 12 months posttransplant. Biopsy-proven acute rejection rate at 24 weeks (primary endpoint, per-protocol analysis) was 15.8% for Tacrolimus BID versus 20.4% for Tacrolimus QD (p = 0.182; treatment difference 4.5%, 95% confidence interval-1.8%, 10.9%, just outside the prespecified 10% noninferiority margin). Kaplan-Meier 12-month patient and graft survival rates were 97.5% and 92.8% for Tacrolimus BID and 96.9% and 91.5% for QD. Both treatment groups showed equally well-maintained renal function at 12 months (mean creatinine clearance approximately 67 mL/min) and similar adverse event profiles. Overall results obtained with either Tacrolimus QD or BID, without antibody induction, were good, supporting use of the once-daily formulation as an effective alternative to the established twice-daily formulation.
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页码:2632 / 2643
页数:12
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