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
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