UK experience of ofatumumab in recurrence of focal segmental glomerulosclerosis post-kidney transplant

被引:9
|
作者
Reynolds, Ben C. [1 ]
Lamb, Angela [1 ]
Jones, Caroline A. [2 ]
Yadav, Pallavi [3 ]
Tyerman, Kay S. [3 ]
Geddes, Colin C. [4 ]
机构
[1] Royal Hosp Children, Dept Pediat Nephrol, Glasgow, Lanark, Scotland
[2] Alder Hey Childrens NHS Trust, Dept Pediat Nephrol, Liverpool, Merseyside, England
[3] Leeds Childrens Hosp, Dept Pediat Nephrol, Leeds, W Yorkshire, England
[4] Queen Elizabeth Univ Hosp, Dept Nephrol, Glasgow, Lanark, Scotland
关键词
Transplant outcomes; Steroid-resistant nephrotic syndrome; Immunosuppression; Plasmapheresis; RESISTANT NEPHROTIC SYNDROME; POSTTRANSPLANT RECURRENCE; GRAFT LOSS; RITUXIMAB; THERAPY; PLASMAPHERESIS; REMISSION; DISEASE;
D O I
10.1007/s00467-021-05248-9
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Background Steroid-resistant nephrotic syndrome (SRNS), commonly caused by focal segmental glomerulosclerosis (FSGS), is associated with progression to stage 5 chronic kidney disease, requirement for kidney replacement therapy and a risk of disease recurrence post-kidney transplantation. Ofatumumab (OFA) is a fully humanised monoclonal antibody to CD20, with similar mechanisms of action to rituximab (RTX). Methods We report a case series of seven UK patients (five paediatric, two adult), all of whom developed FSGS recurrence after kidney transplantation and received OFA as part of their therapeutic intervention. All also received concomitant plasmapheresis. The 2-year outcome of these seven patients is reported, describing clinical course, kidney function and proteinuria. Results Four patients (all paediatric) achieved complete urinary remission with minimal proteinuria 12 months post-treatment. Three of those four also had normal graft function. Two patients showed partial remission-brief improvement to non-nephrotic proteinuria (197 mg/mmol) in one patient, maintained improvement in kidney function (estimated glomerular filtration rate 76 ml/min/1.73 m(2)) in the other. One patient did not demonstrate any response. Conclusions OFA may represent a useful addition to therapeutic options in the management of FSGS recurrence post-transplantation, including where RTX has shown no benefit. Concomitant plasmapheresis in all patients prevents any definitive conclusion that OFA was the beneficial intervention.
引用
收藏
页码:199 / 207
页数:9
相关论文
共 50 条
  • [31] Cyclophosphamide as a Treatment for Focal Segmental Glomerular Sclerosis Recurrence in a Kidney Transplant Patient
    Al-Jehani, Mariann H.
    Al-Husayni, Faisal
    Aljabri, Abdullah
    AlMaghraby, Hatim Qasim
    Banamah, Turki A.
    AMERICAN JOURNAL OF CASE REPORTS, 2021, 22 : 1 - 5
  • [32] Post-transplant recurrence of focal segmental glomerular sclerosis: consensus statements
    Raina, Rupesh
    Jothi, Swathi
    Haffner, Dieter
    Somers, Michael
    Filler, Guido
    Vasistha, Prabhav
    Chakraborty, Ronith
    Shapiro, Ron
    Randhawa, Parmjeet S.
    Parekh, Rulan
    Licht, Christopher
    Bunchman, Timothy
    Sethi, Sidharth
    Mangat, Guneive
    Zaritsky, Joshua
    Schaefer, Franz
    Warady, Bradley
    Bartosh, Sharon
    Mcculloch, Mignon
    Alhasan, Khalid
    Urban, Agnieszka Swiatecka
    Smoyer, William E.
    Chandraker, Anil
    Yap, Hui Kim
    Jha, Vivekanand
    Bagga, Arvind
    Radhakrishnan, Jai
    KIDNEY INTERNATIONAL, 2024, 105 (03) : 450 - 463
  • [33] Pre-transplant angiotensin receptor II type 1 antibodies and risk of post-transplant focal segmental glomerulosclerosis recurrence
    Mujtaba, Muhammad A.
    Sharfuddin, Asif A.
    Book, Benita L.
    Goggins, William C.
    Khalil, Ali A.
    Mishler, Dennis P.
    Fridell, Johnathan A.
    Yaqub, Muhammad S.
    Taber, Tim E.
    CLINICAL TRANSPLANTATION, 2015, 29 (07) : 606 - 611
  • [34] Treatment of recurrent focal segmental glomerulosclerosis post-kidney transplantation in Australian and New Zealand children: A retrospective cohort study
    Francis, Anna
    Didsbury, Madeleine
    McCarthy, Hugh
    Kara, Tonya
    PEDIATRIC TRANSPLANTATION, 2018, 22 (05)
  • [35] Focal segmental glomerulosclerosis in pediatric kidney transplantation: 30years' experience
    Cleper, Roxana
    Krause, Irit
    Bar Nathan, Nathan
    Mor, Maya
    Dagan, Amit
    Weissman, Irith
    Frishberg, Yaakov
    Rachamimov, Ruty
    Mor, Eitan
    Davidovits, Miriam
    CLINICAL TRANSPLANTATION, 2016, 30 (10) : 1324 - 1331
  • [36] Focal Segmental Glomerulosclerosis and Kidney Transplantation
    Gheith, Osama
    Hassan, Rashad
    IRANIAN JOURNAL OF KIDNEY DISEASES, 2013, 7 (04) : 257 - 264
  • [37] Success with plasmapheresis treatment for recurrent focal segmental glomerulosclerosis in pediatric renal transplant recipients
    Straatmann, Caroline
    Kallash, Mahmoud
    Killackey, Mary
    Iorember, Franca
    Aviles, Diego
    Bamgbola, Oluwatoyin
    Carson, Thomas
    Florman, Sander
    Vehaskari, Matti V.
    PEDIATRIC TRANSPLANTATION, 2014, 18 (01) : 29 - 34
  • [38] Successful Treatment of Recurrent Focal Segmental Glomerulosclerosis After Transplantation in Children: A Single-Center Experience
    Alhasan, K. A.
    Alherbish, A.
    Osman, A.
    Kari, J. A.
    Almojalli, H.
    TRANSPLANTATION PROCEEDINGS, 2019, 51 (02) : 517 - 521
  • [39] Recurrence of Focal and Segmental Glomerulosclerosis After Transplantation
    Canaud, Guillaume
    Delville, Marianne
    Legendre, Christophe
    TRANSPLANTATION, 2016, 100 (02) : 284 - 287
  • [40] Focal Segmental Glomerulosclerosis Recurrence in the Renal Allograft
    Leca, Nicolae
    ADVANCES IN CHRONIC KIDNEY DISEASE, 2014, 21 (05) : 448 - 452