European Society of Pediatric Nephrology survey on current practice regarding recurrent focal segmental glomerulosclerosis after pediatric kidney transplantation

被引:13
作者
Bouts, Antonia [1 ]
Veltkamp, Floor [1 ]
Toenshoff, Burkhard [2 ]
Vivarelli, Marina [3 ]
机构
[1] AMC, Emma Childrens Hosp, Dept Pediat Nephrol, Amsterdam, Netherlands
[2] Univ Childrens Hosp Heidelberg, Dept Pediat 1, Heidelberg, Germany
[3] Bambino Gesu Childrens Hosp & Res Inst, Div Nephrol & Dialysis, Rome, Italy
关键词
children; focal segmental glomerulosclerosis; kidney transplantation; recurrence; steroid resistant nephrotic syndrome; RESISTANT NEPHROTIC SYNDROME; RENAL-TRANSPLANTATION; GLOMERULAR SCLEROSIS; NPHS2; MUTATION; RITUXIMAB; CHILDREN; PODOCIN; CYCLOSPORINE; RECIPIENTS; THERAPY;
D O I
10.1111/petr.13385
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Introduction: Primary FSGS is an important cause of ESRD in children. FSGS recurrence after kidney transplantation is associated with early graft loss. No guidelines for treatment of FSGS recurrence exist. We conducted a survey to gain insight into variation of treatment between centers. Methods: A survey was sent to all members of the ESPN on behalf of the "Renal Transplantation" and "Idiopathic Nephrotic Syndrome" working groups. Results: Fifty-nine nephrologists from 31 countries responded, reporting 807 FSGS patients, with 241 (30%) FSGS recurrences after transplantation. Recurrence varied from 0% to 100% between respondents. Native nephrectomy before or during transplantation was performed, respectively, always (37%), never (39%), or on clinical indication (17%). Half of the respondents started preventive treatment before transplantation, using PF (n = 10); R (n = 4); PF or IA, plus R (n = 9); cyclosporine (n = 2); or unknown (n = 4). Immunosuppressive therapy for patients without known mutations consisted of a combination of steroids, tacrolimus/cyclosporine, and MMF, with or without IL-2R-blockade in, respectively, 61% and 86% of the respondents. Sixty-three percent applied a similar regimen to patients with known mutations. FSGS recurrence was treated with PF or IA, plus R by 66% of respondents; 54% observed no response. Complete remission in > 50% of patients was reported by 41% of the respondents. Discussion: FSGS recurrence after transplantation is common, but varies greatly between centers. We found great variability in preventive and therapeutic treatment regimens. Future research should focus on predisposing factors, including biopsy findings and genetic mutations, and standardized treatment.
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页数:8
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共 43 条
[1]   Rituximab and Therapeutic Plasma Exchange in Recurrent Focal Segmental Glomerulosclerosis Postkidney Transplantation [J].
Alasfar, Sami ;
Matar, Dany ;
Montgomery, Robert A. ;
Desai, Niraj ;
Lonze, Bonnie ;
Vujjini, Vikas ;
Estrella, Michelle M. ;
Dieck, John Manllo ;
Khneizer, Gebran ;
Sever, Sanja ;
Reiser, Jochen ;
Alachkar, Nada .
TRANSPLANTATION, 2018, 102 (03) :e115-e120
[2]   Treatment by immunoadsorption for recurrent focal segmental glomerulosclerosis after paediatric kidney transplantation: a multicentre French cohort [J].
Allard, Lise ;
Kwon, Theresa ;
Krid, Saoussen ;
Bacchetta, Justine ;
Garnier, Arnaud ;
Novo, Robert ;
Deschenes, Georges ;
Salomon, Remi ;
Roussey, Gwenaelle ;
Allain-Launay, Emma .
NEPHROLOGY DIALYSIS TRANSPLANTATION, 2018, 33 (06) :954-963
[3]   Outcomes after renal transplantation for FSGS in children [J].
Baum, MA .
PEDIATRIC TRANSPLANTATION, 2004, 8 (04) :329-333
[4]   Recurrent nephrotic syndrome in homozygous truncating NPHS2 mutation is not due to anti-podocin antibodies [J].
Becker-Cohen, R. ;
Bruschi, M. ;
Rinat, C. ;
Feinstein, S. ;
Zennaro, C. ;
Ghiggeri, G. M. ;
Frishberg, Y. .
AMERICAN JOURNAL OF TRANSPLANTATION, 2007, 7 (01) :256-260
[5]   Ofatumumab in post-transplantation recurrence of a pediatric steroid-resistant idiopathic nephrotic syndrome [J].
Bernard, Josselin ;
Bruel, Alexandra ;
Allain-Launay, Emma ;
Dantal, Jacques ;
Roussey, Gwenaelle .
PEDIATRIC TRANSPLANTATION, 2018, 22 (04)
[6]   Recurrence of focal segmental glomerulosclerosis after renal transplantation in patients with mutations of podocin [J].
Bertelli, R ;
Ginevri, F ;
Caridi, G ;
Dagnino, M ;
Sandrini, S ;
Di Duca, M ;
Emma, F ;
Sanna-Cherchi, S ;
Scolari, F ;
Neri, TM ;
Murer, L ;
Massella, L ;
Basile, G ;
Rizzoni, G ;
Perfumo, F ;
Ghiggeri, GM .
AMERICAN JOURNAL OF KIDNEY DISEASES, 2003, 41 (06) :1314-1321
[7]   Deriving and understanding the risk of post-transplant recurrence of nephrotic syndrome in the light of current molecular and genetic advances [J].
Bierzynska, Agnieszka ;
Saleem, Moin A. .
PEDIATRIC NEPHROLOGY, 2018, 33 (11) :2027-2035
[8]   Genomic and clinical profiling of a national nephrotic syndrome cohort advocates a precision medicine approach to disease management [J].
Bierzynska, Agnieszka ;
McCarthy, Hugh J. ;
Soderquest, Katrina ;
Sen, Ethan S. ;
Colby, Elizabeth ;
Ding, Wen Y. ;
Nabhan, Marwa M. ;
Kerecuk, Larissa ;
Hegde, Shivram ;
Hughes, David ;
Marks, Stephen ;
Feather, Sally ;
Jones, Caroline ;
Webb, Nicholas J. A. ;
Ognjanovic, Milos ;
Christian, Martin ;
Gilbert, Rodney D. ;
Sinha, Manish D. ;
Lord, Graham M. ;
Simpson, Michael ;
Koziell, Ania B. ;
Welsh, Gavin I. ;
Saleem, Moin A. .
KIDNEY INTERNATIONAL, 2017, 91 (04) :937-947
[9]   Podocin-related mechanisms in posttransplantation recurrence of focal segmental glomerulsclerosis [J].
Caridi, G. ;
Dagnino, M. ;
Sanna-Cherchi, S. ;
Perfumo, F. ;
Ghiggeri, G. M. .
TRANSPLANTATION PROCEEDINGS, 2006, 38 (10) :3486-3490
[10]   A randomized trial of cyclosporine in patients with steroid-resistant focal segmental glomerulosclerosis [J].
Cattran, DC ;
Appel, GB ;
Hebert, LA ;
Hunsicker, LG ;
Pohl, MA ;
Hoy, WE ;
Maxwell, DR ;
Kunis, CL .
KIDNEY INTERNATIONAL, 1999, 56 (06) :2220-2226