Initial Dosage Range of Tacrolimus by Genotyping in Chinese Renal Transplantation

VISITS

The participation of the patient in this study will be 3 months. For this period, 9 visits are planned

•Before transplantation

Visit 1: inclusion visit(in the 4-7 days before transplantation),A blood taking will be carried out on EDTA tube for CYP 3A5 genotyping in the 4-7 days before renal transplantation.

• After transplantation

Visit 2: D3

Visit 3: D5

Visit 4: D7

Visit 5: D14

Visit 6: D21

Visit 7: M1 + - 3 days

Visit 8: M2 + - 3 days

Visit 9: M3 + - 3 days

Treatment

After transplantation, the patients will be treated by MMF, corticosteroids and tacrolimus at a dosage adapted to their genotype(CYP3A5*1/*1 type and CYP3A5*1/*3 type administer 0.15mg/kg/d，CYP3A5*3/*3 type administer 0.08mg/kg/d).

The MMF will be given according to weight in 3 months after transplantation as follows:

below 50 kilogram(kg) 0.25g bid (0.5g pre day)

50~70kg 0.50g bid (1.0g pre day)

70~90kg 0.75g bid (1.5g pre day)

Exceed 90kg 1.0g bid (2.0g pre day)

Corticosteroid therapy in decreasing amount as follows:

D0 - D15: 20 Mg

D16 - D30: 15 Mg

D30 - D45: 10 Mg

D46 - M3 5 Mg

The determination of tacrolimus blood concentration will be carried out on Day 3,5,7,14,18,21,28,35,49,63,77,90. The daily amounts of Tacrolimus could be modified if necessary to reach the desired blood concentrations. The total duration of the study for a patient is 3 months after transplantation.

If the present study is able to confirm an advantage for a genotype-driven algorithm, in terms of improved efficiency, therapeutic efficacy, especially, safety, a pharmacogenetics approach to dosing can be recommended as the basis wide quality improvement initiative that should improve patient outcomes, reduce resource use (costs of achieving safe and therapeutic immunosuppression), and reduce adverse clinical events.

Inclusion criteria

• Patients of renal inadequacy , necessary to receive renal transplantation , male or female , 18 to 65 years old;
• Patients receiving a first isolated renal graft with administration of FK506;
• Patient willing to provide informed consent prior to the specimen collection procedure.

Exclusion criteria

• Patients who received another clinical pharmaceutical study less than 3 months before the entry in this study , and who have already completed or dropped out of this study.
• Patients with contraindications of FK506 in immunosuppressive therapy : being in pregnancy and being allergic or intolerant with FK506 or other macrolides.
• Patients suffering from severe diseases of cardiovascular system (essential hypertension), liver (anamnesis of type B hepatitis , type C hepatitis) , hemopoietic system , nervous system , and psychotics.
• Patients interfered with their blood concentrations of FK506 by administration of cytochrome P4503A4 and P4503A5 enzyme inhibitors , such as lidocaine , midazolam , nicardipine , niludipine , cortisone , itraconazole , fluconazole , ketoconazole , miconazole , clotrimazole ，Bromocriptine and so on.
• Patients having anaemia (hemoglobin lower than 7g/dl).
• Patients Diagnosed DM.
• Patients interfered with their capacity to absorb FK506 by anorexia nervosa , malabsorption syndrome or gastro-intestinal resection according to the viewpoint of the investigators.
• Patients who lacks understanding of the medicinal knowledge of tacrolimus and the risks of the study according to the viewpoint of the investigators.
• Patients with allergic constitution or a history of serious allergy.
• Patients with bad compliance according to viewpoint of the investigators.