DESYRE: Systematic Transplantectomy Versus Conventional Care After Kidney Graft Failure

Sponsor
Hospices Civils de Lyon (Other)
Overall Status
Recruiting
CT.gov ID
NCT01817504
Collaborator
(none)
118
20
2
128
5.9
0

Study Details

Study Description

Brief Summary

Our hypothesis is early and systematic transplantectomy under a well-conducted immunosuppression is associated with a decreased risk of anti-HLA immunization against a conservative attitude including a gradual reduction of immunosuppression, with or without a transplantectomy performed for cause (clinical event).

Observation or Investigation Method Used :
The study is :
  • multicenter

  • prospective

  • open

  • randomized: patients are divided into two parallel groups:

  • study group: transplantectomy within six weeks after return to dialysis, antiproliferatives stop at the start of dialysis, Maintenance anticalcineurin-based-immunosuppression without dose reduction up to two weeks after transplantectomy. Abrupt discontinuation of anticalcineurin two weeks after transplantectomy. Corticosteroids: 5mg per day until one month after transplantectomy then stop within one month.

  • control group: No systematic transplantectomy. Antiproliferatives stop at the start of dialysis.Anticalcineurins half dose for 3 months, ¼ dose for 3 months and then stop. Corticosteroids:5 mg per day for 6 months, and then tapered and stop within 3 months.

In the case of transplantectomy for cause in the control group, immunosuppression will be continued at the maintenance dose during the current surgical procedure, and withdrawn two weeks later,similary to systematic transplantectomy.

Condition or Disease Intervention/Treatment Phase
  • Procedure: Systematic transplantectomy
  • Procedure: Progressive reduction of immunosuppression
N/A

Study Design

Study Type:
Interventional
Anticipated Enrollment :
118 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Supportive Care
Official Title:
Interest of Systematic Transplantectomy Versus Conventional Care After Kidney Graft Failure
Actual Study Start Date :
Mar 1, 2013
Anticipated Primary Completion Date :
Nov 1, 2023
Anticipated Study Completion Date :
Nov 1, 2023

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: Study group

The study group corresponds to systematic transplantectomy under immunosuppressive therapy within two months after return to dialysis,

Procedure: Systematic transplantectomy
Transplantectomy within two months after return to dialyse. Antiproliferatives stop at the start of dialysis. Maintenance basic immunosuppressive treatment without dose reduction up to two weeks after transplantectomy. Abrupt discontinuation of the basic immunosuppressive treatment ttwo weeks after transplantectomy. Maintenance corticosteroids at 5mg per day until one month after transplantectomy then stop corticosteroids within one month.

Other: Control group

The control group corresponds to progressive reduction of immunosuppression without systematic transplantectomy after return to dialysis

Procedure: Progressive reduction of immunosuppression
Progressive reduction of immunosuppression. Transplantectomy for cause only. Antiproliferatives withdrawn at the start of dialysis. Maintenance of anticalcineurin or mTOR inhibitors half dose for 3 months, ¼ dose for 3 months and then stop. Maintenance corticosteroids for 6 months up to 5 mg per day, and then soft stop in 3 months. In case of transplantectomy by reason in the control group, basic immunosuppression will be continued at the maintenance dose during the current surgical procedure, and withdrawn two weeks later, similary to the strategy used in the study group.

Outcome Measures

Primary Outcome Measures

  1. Anti HLA Immunization assessed by Luminex assay [12 months (M12)]

    Evaluate the interest of a transplantectomy early (<2 months after return to dialysis) and systematic under immunosuppressive in renal transplant patients after loss of renal graft function in terms of anti-HLA immunization (measured by Luminex test) a year after loss of renal graft function and return to dialysis in the renal transplant patient. Proportion of patients who developed HLA immunization (DSA)after systematic transplantectomy under immunosuppression versus progressive reduction of immunosuppression without transplantectomy

Secondary Outcome Measures

  1. Kinetics anti-HLA antibodies after transplantectomy [12 months after inclusion]

    Determine the kinetics of new onset anti-HLA antibodies at D0, D15, D30, M3, M6, M9 after systematic or for cause transplantectomy and in the year following graft failure and the proportion of immunized patients during the first 6 months after dialysis. HLA antibodies will be assessed by Luminex test. The specificity of antibodies against HLA I or HLA II will be determined, as well as Mean Immunofluorescence Intensity in each case.

  2. Morbidity and mortality after transplantectomy [12 months after inclusion]

    Determine the morbidity and mortality after transplantectomy according to its indication, systematic or for cause (transplantectomy indications in the control group: persistent pain graft, unexplained fever, hematuria, inflammation or unexplained anemia ).

  3. Measuring the impact of systematic transplantectomy on mortality, inflammation, nutritional status, anemia, hypertension and cardiovascular risk factors [12 months]

    The following parameters will be measured at D0, M1, M3, M6, M9 and M12 after return to dialysis during the first year after kidney graft failure: CRP, pre-albuminemia, albuminemia, BMI, hemoglobin, hematocrit, blood pressure, cholesterol, LDL cholesterol and triglyceride.

  4. Infectious comorbidity [12 months]

    The impact of early cessation of immunosuppression on infectious complications after kidney graft failure will assessed. For each patient, origin of infection, bacterial, viral, fungal, will determined. The total number of infection episodes during the first year will be analyzed in the two groups.

  5. Costs of two strategies [12 months after inclusion]

    To evaluate the medico-economic impact of each conservation strategy in the management of patients who return to dialysis

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 75 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Age ≥ 18 Years.

  • Patients affiliated to health protection system, social security in France or any similar regimen.

  • Renal transplant patient with end-stage transplantation, regardless of the number of previous transplants.

  • Patient receiving immunosuppressive protocol based on anticalcineurin or mTOR inhibitors

  • Patient should have resume hemodialysis within 4 weeks

  • Duration of transplantation more than one year

  • Patient with asymptomatic graft

  • immunogenic potential residual >50% (calculated PIR during the re-dialysis)

  • Patient not covered by any measure of legal protection.

Exclusion Criteria:
  • Immunogenic potential residual <50%

  • Graft infection uncontrolled by treatment

  • Active infectious pathology

  • Inflammatory graft

  • Uncontrolled arterial hypertention

  • Inflammatory syndrome of undetermined origin with CRP>50mg/l

  • Fever of unknown origin for more than 8 days T>38°C

  • Contra-indication to surgery

  • AVK treatment

  • Patient candidate for a living donor within 12 months

  • Monotherapy with calcineurin inhibitors or mTOR inhibitors

  • Treatment directed against the humoral response in the 6 months preceding the recovery of dialysis (Rituximab IV-Ig or high doses)

  • Presence of another transplant (pancreas, liver, heart, lung)

Contacts and Locations

Locations

Site City State Country Postal Code
1 Service de Néphrologie, Médecine interne, Hémodialyse, Transplantation Rénale, Hôpital Sud Amiens France 80054
2 Service de Néphrologie, Dialyse et Transplantation - Hôpital Jean Minjoz Besançon France 25030
3 Service de Néphrologie - Hôpital de La Cavale blanche Brest France 29609
4 Service de Néphrologie et Transplantation Rénale, CHU Gabriel Montpied Clermont-Ferrand Cedex France 63000
5 Hôpitaux Civils de Colmar Colmar France 68024
6 Service de Néphrologie -Dialyse-Transplantation, Hôpital Michallon Grenoble Cedex France 38043
7 Centre Hospitalier de Haguenau Haguenau France 67504
8 Centre Hospitalier départemental Vendée - Site de la Roche-sur-Yon La Roche-sur-Yon France 85925
9 Service de Néphrologie - Hôpital Claude Huriez Lille France 59000
10 Transplantation Department, Hôpital Edourad Herriot Lyon France 69003
11 Service de Néphrologie et Transplantation Rénale - Hôpital Lapeyronie Montpellier France 34295
12 Institut de Transplantation, Urologie et Néphrologie - CHU Nantes Nantes France 44093
13 Unité de Transplantation Rénale - Hôpital de l'Archet Nice France 06202
14 Urgence Néphrologique et Transplantation Rénale - Hôpital Tenon Paris France 75020
15 Service de Néphrologie, Centre Hospitalier Lyon Sud Pierre Bénite France 69310
16 Service de Néphrologie-Dialyse, Centre Hospitalier d'Annecy Pringy France 74374
17 Service de Néphrologie, Dialyse et Transplantation Rénale, Hôpital Nord Saint-Etienne France 42055
18 Service de Néphrologie et Transplantation Rénale - Nouvel Hôpital Civil Strasbourg France 67091
19 Département de Néphrologie et Transplantation d'Organes - Hôpîtal Rangueil Toulouse France 31059
20 Service de Néphrologie, Immunologie Clinique - CHU Bretonneau Tours France 37044

Sponsors and Collaborators

  • Hospices Civils de Lyon

Investigators

  • Principal Investigator: Emmanuel MORELON, MD, Transplantation Department, Hopital Edouard Herriot, Hospices Civils de Lyon

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Hospices Civils de Lyon
ClinicalTrials.gov Identifier:
NCT01817504
Other Study ID Numbers:
  • 2012.714
First Posted:
Mar 25, 2013
Last Update Posted:
Jan 27, 2022
Last Verified:
Jan 1, 2022
Keywords provided by Hospices Civils de Lyon

Study Results

No Results Posted as of Jan 27, 2022