TACrolimus in Renal Transplantation: Individualization by Pharmacogenetic

Inclusion criteria

• Patients, male or female, 18 to 65 years old.
• Patients receiving a first or a second isolated renal graft coming from a donor alive or deceased,
• The patients in age to procreate must have a negative test of pregnancy before being included in this study and will have to agree to use effective contraceptive measurements throughout the study.
• Patients able to include/understand the aims and the risks of the study, having been fully informed and having given their writing consent to take part in this study. Patients unable to write and/or read but having fully understood the oral information given by the investigator and having given their oral consent in the presence of an independent witness.

Non-inclusion criteria

• Patients who receive several grafts.
• Patients requiring a treatment by azathioprin.
• Pregnant woman or nursing mother
• Patients receiving an incompatible graft ABO.
• Patients receiving or requiring immunosuppressant drugs prohibited by the protocol.
• Patients with a peak of historical antibody equal to or greater than 50% of the panel.
• Patients suffering from serious gastro-intestinal disorders which interfere with their capacity to receive or to absorb an oral form and patients presenting severe diarrhoea.
• Patients with symptomatic GI ulcer
• HIV or HTLV1 positive patients or their donors
• Patients presenting or having presented in the 5 last years one or several malignant tumours, except baso or spinocellular cutaneous epithelioma successfully treated.
• Patients with systemic infections requiring a treatment at the entry in the study.
• Patients having a leukocyte numeration lower than 2,5.109/l or haemoglobin lower than 5g/dl.
• Patients with drug-addiction whatever it is, or psychiatric disorder which, according to the point of view of the investigator, could invalidate the communication with investigator or interfere with the compliance of the patient.
• Patients who take part simultaneously in another therapeutic test or who received a study treatment less than 30 days before the entry in this study.
• Patients having already been included in this study.
• Patients allergic or intolerant with corticoids, macrolides, Tacrolimus, mycophenolate mofetil or basiliximab

The inclusion period is planned for 15 month. The inclusion of the patients will take place before transplantation. After transplantation, a centralized genotyping of CYP3A5 will be carried out for each patient. A sample of blood will be taken the day of transplantation.

The randomization will be carried out according to a 1:1 mode, by unequal blocks and stratified on the center according to group A (Tacrolimus given at D7,dosage:0,20 mg/kg/d) versus group B (managed Tacrolimus given at D7 dosage adapted to genotype CYP3A).

VISITS

The participation of the patient in this study will be 3 months. For this period, 7 visits are planned. D0 being considered as the day of the closing of the skin.

• Before transplantation Visit 1: inclusion visit(in the 4 days before transplantation) The day of transplantation a blood taking will be carried out on EDTA tube for CYP 3 A5 genotyping
• After transplantation (D0 = day of closing of the skin)
• Visit 2: J6 (randomization)
• Visit 3: J10
• Visit 4: J14
• Visit 5: M1 + - 3 days
• Visit 6: M2 + - 3 days
• Visit 7: M3 + - 7 days

TREATMENTS:

-Tacrolimus In the two arms of treatment Tacrolimus will be given at D7 post transplantation according to the group of randomization.

The first dosage schedule of Tacrolimus will be different according to the group of randomization:

• Group A: 0,10 mg/kg 2 times per day for all the patients
• Group B:
• 0,125 mg/kg 2 times per day (CYP3A5 *1/*1 or *1/*3)
• 0,075 mg/kg 2 times per day (CYP3A5*3/*3)

A first residual blood concentration (C0) of Tacrolimus will be evaluated after 6 administrations of Prograf®, at D10. The dosage schedule of Tacrolimus will then be adapted freely according to the therapeutic pharmacological follow-up of Tacrolimus specified in the protocol, that is to say 10 to 15 ng/ml, whatever the group of randomization.

• Basiliximab All the patients will receive two injections of basiliximab per intravenous way (first injection before transplantation and second injection at D4),20 Mg by intake.
• Corticotherapy in decreasing amount as follows:
• D0: 500 Mg
• D1: 125 Mg
• D2 - D15: 20 Mg
• D16 - M1: 15 Mg
• M1 - M3: 10 Mg
• MMF The MMF will be given 3 gr. per day during the first 15 days, then 2 G per day adapted according to the clinical and biological tolerance.

During this study the following treatments will not be authorized :

• immunosuppressants other than those proposed; ciclosporin, sirolimus, azathioprine, plasmatic exchanges; intravenous immunoglobulins.
• Gastric bandages [gastric protections (inhibitors of the H+ pump) are authorized].
• Treatments presenting an interaction with P-glycoprotein or cytochromes P450 3A
• Any drug not having a marketing authorization. All the concomitant drugs taken by the patient during this study must be written in the CRF as all the drugs the patient would have taken in the 7 days before transplantation.

The analysis of this test will be done at the end of the inclusion on all the patients according to the principle of Intention To Treat Analysis.

The patients being able to be excluded from this analysis will be:

• patients not having taken no amount of the evaluated drug
• patients without data collected after the randomization

An analysis per-protocol will be carried out. From this analysis could be excluded in an additional way to the preceding analysis:

• declared patients not compliants
• patients who left the study for another reason that the inefficiency of the treatment or an undesirable event
• patients having taken during the study one or more prohibited treatments which can influence the effectiveness.

STATISTIC

Calculation of the necessary number of subjects:

One defines as a success: The event "blood concentration of Tacrolimus is between 10 and 15 ng/ml after 6 administrations per bone" One defines as a failure: The event "blood concentration of Tacrolimus is not between 10 and 15 ng/ml after 6 administrations per bone".

The awaited percentage of event is 40% in group A (dosage schedule of Tacrolimus according to recommendations: 0,20/kg/d).

It is made the assumption that the adaptation of the dosage schedule of Tacrolimus according to genetics will increase the success rate to 60%.

By setting an alpha risk = 5%, a beta risk = 10%, in bilateral formulation, by balancing the randomization (1/1), it are necessary to include 140 subjects by group to show an absolute difference of 20% of success between the 2 groups, that is to say 1 year of inclusion and 1 year and 3 months of study.