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UK experience of ofatumumab in recurrence of focal segmental glomerulosclerosis post-kidney transplant.
Reynolds, Ben C; Lamb, Angela; Jones, Caroline A; Yadav, Pallavi; Tyerman, Kay S; Geddes, Colin C.
Afiliación
  • Reynolds BC; Department of Pediatric Nephrology, Royal Hospital for Children, Glasgow, UK. ben.reynolds@ggc.scot.nhs.uk.
  • Lamb A; Department of Pediatric Nephrology, Royal Hospital for Children, Glasgow, UK.
  • Jones CA; Department of Pediatric Nephrology, Alder Hey Children's NHS Trust, Liverpool, UK.
  • Yadav P; Department of Pediatric Nephrology, Leeds Children's Hospital, Leeds, UK.
  • Tyerman KS; Department of Pediatric Nephrology, Leeds Children's Hospital, Leeds, UK.
  • Geddes CC; Department of Nephrology, Queen Elizabeth University Hospital, Glasgow, UK.
Pediatr Nephrol ; 37(1): 199-207, 2022 01.
Article en En | MEDLINE | ID: mdl-34383125
ABSTRACT

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 m2) 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.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Glomeruloesclerosis Focal y Segmentaria / Trasplante de Riñón / Anticuerpos Monoclonales Humanizados Límite: Adult / Child / Humans País/Región como asunto: Europa Idioma: En Revista: Pediatr Nephrol Asunto de la revista: NEFROLOGIA / PEDIATRIA Año: 2022 Tipo del documento: Article País de afiliación: Reino Unido

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Glomeruloesclerosis Focal y Segmentaria / Trasplante de Riñón / Anticuerpos Monoclonales Humanizados Límite: Adult / Child / Humans País/Región como asunto: Europa Idioma: En Revista: Pediatr Nephrol Asunto de la revista: NEFROLOGIA / PEDIATRIA Año: 2022 Tipo del documento: Article País de afiliación: Reino Unido