Eculizumab Treatment on GC3 Recurrence on Renal Graft.
1Department of Nephrology, Dialysis and Transplantation, Hôpital Lapeyronie, Montpellier University Hospital, Montpellier, France
2Department of Nephrology, Dialysis and Transplantation, Lille, France
3Department of Nephrology, Dialysis and Renal Transplantation, Rouen, France
4Transplantation Rénale, Necker Hospital, Paris, France
5Immunology, Hopital Européen Georges Pompidou, Paris, France
Meeting: 2017 American Transplant Congress
Abstract number: B157
Keywords: Kidney transplantation, Recurrence
Session Information
Session Name: Poster Session B: Kidney Complications II
Session Type: Poster Session
Date: Sunday, April 30, 2017
Session Time: 6:00pm-7:00pm
Presentation Time: 6:00pm-7:00pm
Location: Hall D1
Clinical C3G recurrence occured in more than 50% after renal transplantation and is the first cause of allograft loss at 5 years post-transplantation. Eculizumab (EC) has been used in severe GC3 on native kidney and in few cases in graft recurrence with contreversal results. The aim of this study was to evaluate EC efficacy in graft GC3 recurrence in French cohort.
We retrospectively analyzed patients who received EC for a clinical GC3 graft recurrence. Clinical recurrence was defined by a proteinuria > 0.5 g/g and/or increasing serum creatinine > 30% from the baseline. Recurrence had to be proven by graft biopsy and was considered by C3 deposits without associated rejection. The efficiency of Ec was evaluated at 3 and 6 months. Partial remission (PR) was defined by stabilization (+/-25%) or improvement of serum creatinine and proteinuria reduction upper than 50%. Complete remission (CR) was defined by a normalized serum creatinin (basal value) and proteinuria lower than 0,5 g/g.
Ten patients received EC for C3G recurrence. Reccurence occured with a median of 56 days. At diagnosis serum creatinin median was 222,5 [mu]mol/L (range : 98-304 [mu]mol/L) and proteinuria was 1 g/g (range : 0,1-6,2 g/g). In all graft biopsies, C3 deposit was positive. At EC initiation median proteinuria was 1,75 g/g (range 0,58-3,97 g/g) and median serum creatinin was 214,5 [mu]mol/L (range 98-304 [mu]mol/L).
At 3 months, 2 patients had their treatment interrupted for ineffectiveness by clinicians and were considered non-responders. At 6 months, 7 patients had a EC-response (4 CR and 3 a PR) and 1 was non-responder. 2 of the three non-responders lost their graft. CR patients are all still under treatment and after a median follow-up of 62,7 months, have a stable renal function and proteinuria < 0,5 g/g suggesting lasting effectiveness.
All of CR under EC patients had at time of diagnosis an acute renal failure, massive proteinuria
Eculizumab is effective in 70% patients with C3G severe clinical recurrence, mostly in patient with acute renal failure and proteinuria. It's an option for clinical C3G recurrence treatment in subset of patients.
CITATION INFORMATION: Jeantet G, Bertrand D, Lionet A, Anglicheau D, Fremeaux-Bacchi V, Le Quintrec M. Eculizumab Treatment on GC3 Recurrence on Renal Graft. Am J Transplant. 2017;17 (suppl 3).
To cite this abstract in AMA style:
Jeantet G, Bertrand D, Lionet A, Anglicheau D, Fremeaux-Bacchi V, Quintrec MLe. Eculizumab Treatment on GC3 Recurrence on Renal Graft. [abstract]. Am J Transplant. 2017; 17 (suppl 3). https://atcmeetingabstracts.com/abstract/eculizumab-treatment-on-gc3-recurrence-on-renal-graft/. Accessed November 22, 2024.« Back to 2017 American Transplant Congress