Tacrolimus to Sirolimus Conversion for Delayed Graft Function (RAPA)

University of Maryland Baltimore (UMB)

Status and phase: Terminated; Phase 4

Conditions: Kidney Transplant; Delayed Graft Function

Treatments: Drug: Sirolimus; Drug: Tacrolimus

Study type: Interventional

Funder types: Other; Industry

Identifiers

NCT00931255

HP-00042201

Details and patient eligibility

About

The objective of this study is to evaluate the safety and efficacy of conversion from tacrolimus to sirolimus early after kidney transplantation in patients with delayed graft function (DGF)and slow graft function (SGF) in improving graft function and delaying chronic allograft nephropathy. The investigators hypothesize that conversion from tacrolimus to sirolimus in renal transplant recipients with DGF/SGF in early months after surgery will improve graft function and decrease the progression of graft fibrosis.

Full description

Eligible study subjects will be randomized into two groups 8-18 weeks after surgery. One group will be maintained on tacrolimus according to the standard of care at our center. In the second group tacrolimus will be converted to sirolimus, with one week overlap between sirolimus therapy and tacrolimus taper. All the deceased donor kidney transplant recipients transplanted at our center who experience DGF/SGF are eligible for inclusion in this study, if they meet the inclusion/exclusion criteria as detailed later.

Data will be collected on patient demographics, duration on dialysis, history of diabetes and chronic hepatitis C, previous transplantation, PRA, donor source, warm and cold ischemia time, donor demographics and comorbidity such as diabetes and hypertension, serum creatinine at the time of organ removal, early graft function, number of dialysis treatments after transplantation, induction agent and immunosuppressive regimen including the dose or level of the drugs at 3, 6, 9, 12, 18, and 24 months. Similar data regarding use of ACE inhibitors/ARBs, erythropoietic agents, number of anti-hypertensives and lipid lowering agents will be collected. In addition, the following tests and procedures will be obtained for this study.

1. GFR measurement by cold iothalamate method at one year after transplantation.
2. Evaluation of routine surveillance graft biopsies for chronic changes at 3 and 12 months posttransplant by morphometric analysis.
3. Spot urine protein, albumin, and creatinine measurement at 3 and 12 months.
4. Estimate GFR at 3, and 12 months using MDRD, CG, and Nankivell formulas
5. Examine the surveillance and indicated biopsies for acute rejection and BK nephropathy.
6. Fasting lipid profile at 3 and 12 months for all patients, and 24 months for those with at least 2 years of follow up.
7. Office blood pressure measurements at 3 and 12 months for all patients, and 24 months for those with at least 2 years of follow up.
8. Measurement of CRP, IL-6, and MCP at 3 and 12 months.

The safety measures will include:

Incidence of leukopenia (WBC < 3000) or thrombocytopenia (PLT < 100,000); hemoglobin level at 12 months; proteinuria at 12 months; incidence of oral aphthous ulcers; incidence of new onset diabetes, incidence of CMV infection and rate of drug withdrawal due to side effects.

Enrollment: 32 patients

Sex: All

Ages: 18 to 80 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

1. Age => 18.
2. Recipient of a deceased donor kidney transplant.
3. Delayed graft function, defined as need for dialysis during first week after surgery or slow graft function, defined as creatinine >=3.0 by post-op day 5 without requiring dialysis
4. Stable serum creatinine for 2 weeks prior to enrollment.
5. Able to give informed consent.
6. Compliant with medical regimen and clinic visits.

Exclusion criteria

1. Episode of acute rejection within 4 weeks prior to enrollment.
2. Calculated GFR < 30 ml/min.
3. Interstitial fibrosis & tubular atrophy in transplant biopsy higher than grade II (Banff"05 update).
4. Proteinuria > 500 mg/24 h or spot urine protein/creatinine > 0.5.
5. Total fasting cholesterol level > 300 mg/dl or triglyceride > 500 mg/dl despite optimal lipid lowering therapy.
6. Recipient of pancreas or liver allografts.
7. Leukopenia (WBC < 3000 mm3) within 2 weeks prior to enrollment.
8. Leukopenia (WBC < 2000 mm3) within 4 weeks prior to enrollment.
9. Thrombocytopenia (platelets count < 100,000/mm3) within 2 weeks prior to enrollment.
10. Unwilling to comply with study protocol.
11. Enrollment in another drug trial that precludes use of sirolimus.
12. Diagnosis of malignancy within 2 years prior to enrollment, except adequately treated non-melanoma skin cancer.
13. For women, pregnancy.
14. Allergy to iodine

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: None (Open label)

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32 participants in 2 patient groups

Tacrolimus

Active Comparator group

Description:

Tacrolimus will be continued with target 12-hour trough level 7-10 ng/ml (tandem mass spectrometry) during the first year and 5-8 during second year.

Treatment:

Drug: Tacrolimus

Sirolimus

Active Comparator group

Description:

5 mg, PO , daily

Treatment:

Drug: Sirolimus