Evaluation of Desensitization Protocols in HLA-incompatible Kidney-transplant Candidates
- Sponsor
- University Hospital, Grenoble
- Study ID
- NCT03507348
- Status
- Terminated
Conditions
- End-stage Renal Disease
- Hla-incompatible Kidney Transplant Candidates
- Kidney Transplantation
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - 65 Years
- Healthy Volunteers
- Not accepted
Interventions
- visits of tocilizumab injection (every 4 weeks, up to 5 visits) — DRUGevery 4 weeks, up to 5 visits (D-170, D-142, D-114, D-86, D-58).
- Rituximab 375 mg/m2 at Day-30 — DRUGRituximab 375 mg/m2 at Day-30
- Rituximab 375 mg/m2 at Day-15 (only for donors living) — DRUGRituximab 375 mg/m2 at Day-15
- Transplant Day-0 — OTHERTRANSPLANTATION
Study Details
Kidney transplantation is the best renal-replacement in the setting of end-stage renal disease. However, some transplant candidates have developed anti-HLA alloantibodies (human leukocyte antigen). When they are numerous and when their strength assessed by mean fluorescence intensity (MFI) is high it is very complicated to find-out a suitable kidney allograft against which the recipient has a negative cross-match. In such a case the only hope for the patient is desensitization therapy, whereby the treatment will decrease anti-HLA alloantibodies below a threshold, i.e. MFI \< 3,000, enabling kidney transplantation without risking antibody-mediated rejection. Desensitization relies on i) apheresis technics in order to withdraw circulating anti-HLA antibodies, and ii) immunosuppression, i.e. rituximab or tocilizumab, targeting B-lymphocytes, and tacrolimus/mycophenolic acid/steroids targeting T-cells. The type of apheresis is guided by the pre-desensitization MFI of anti-HLA alloantibodies, e.g. double filtration plasmapheresis or semispecific immunoadsorption. Likely the choice between rituximab and tocilizumab depends also on predesensitization anti-HLA antibody MFIs. At the end of the desensitization process, the patient will be able to get a kidney transplant either from a live-donor or from a deceased donor.
Key Dates
- Start date
- Jul 1, 2018
- Status verified
- Mar 2020
- Primary completion
- Nov 21, 2019
- Completion
- Nov 21, 2019
Study Design
- Enrollment
- 8 participants (actual)
- Allocation
- NON_RANDOMIZED
- Intervention model
- PARALLEL
- Primary purpose
- OTHER
Arms
- Other: Desensitization with Tocilizumab and rituximab (MFI >15000)
- Other: Desensitization with Rituximab only (MFI<15000)
Primary Outcome Measure
Description of the results of the strategy of desensitization in patients who will access to kidney transplantation from deceased or living donors. [ Time Frame: at day 1 start of desensitization, at day 0 of Graft ]
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