4.4 Article

Treatment of post-transplant recurrent FSGS in children using plasmapheresis and augmentation of immunosuppression

Journal

BMC NEPHROLOGY
Volume 23, Issue 1, Pages -

Publisher

BMC
DOI: 10.1186/s12882-022-02768-w

Keywords

Focal and segmental glomerulosclerosis; Renal transplantation; Recurrence; Plasmapheresis; Cyclophosphamide; Pediatric

Funding

  1. International Society of Nephrology (ISN) through the ISN Sister Renal Center Program: Boston Children's Hospital USA Fundacion Valle del Lili, Cali, Colombia

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This study retrospectively observed a treatment protocol for recurrent FSGS, showing a high remission rate in pediatric renal transplant patients. The combination of plasmapheresis, cyclophosphamide, and standard immunosuppression treatment was found to be effective in improving remission rates for FSGS.
Background Up to 60% of pediatric renal transplant recipients with end-stage renal disease due to primary focal and segmental glomerulosclerosis (FSGS) may develop recurrent disease. Such recurrence is associated with poor prognosis if no remission is achieved. We report a single center experience with a protocol based on plasmapheresis and increased immunosuppression that resulted in a high long-lived remission rate. Methods This retrospective cohort study included consecutive pediatric renal transplant patients with recurrent FSGS treated with a standardized protocol using plasmapheresis and cyclophosphamide to supplement usual post-transplant immunosuppression with calcineurin inhibitors and steroids. Relapse was defined as urinary protein/creatinine ratio > 1.0 g/g and remission as < 0.5 g/g. Results Seventeen patients with FSGS recurrence post-transplant were treated. All had therapy resistant FSGS in native kidneys and had been on dialysis from 4 to 10 years. Of the 17, one died perioperatively from a pulmonary thromboembolism. Fifteen others achieved a complete remission within 3 months of treatment for FSGS recurrence. After a median follow-up period of 4 years, there were no recurrences of significant proteinuria. One patient achieved remission with rituximab. Conclusion The addition of plasmapheresis and cyclophosphamide to a calcineurin- and steroid-based immunosuppression regime was highly successful in inducing high remission rates with recurrent FSGS. Prospective trials are needed to evaluate further the efficacy of increased immunosuppression along with plasmapheresis in this setting.

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