Evidence map›Paper›PMID 40212825›Full record

ArticleClinical kidney journal2025

Subcutaneous ofatumumab in recurrent focal segmental glomerulosclerosis after kidney transplantation.

Shirley Pollack, Moran Plonsky-Toder, Rami Tibi, Irina Libinson-Zebegret, Renata Yakobov, Daniella Magen

Abstract read
In one paragraph

Article in Clinical kidney journal, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Review
  2. Targeting CD20 for B-cell Depletion in Autoimmune Kidney Disease: Next Generation.BioDrugs : clinical immunotherapeutics, biopharmaceuticals and gene therapy · 2025
    Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

Shirley PollackPediatric Nephrology Institute, Ruth Children's Hospital, Rambam Health Care Campus, Haifa, Israel.ORCID https://orcid.org/0000-0002-9129-3165
Moran Plonsky-ToderPediatric Nephrology Institute, Ruth Children's Hospital, Rambam Health Care Campus, Haifa, Israel.
Rami TibiPediatric Nephrology Institute, Ruth Children's Hospital, Rambam Health Care Campus, Haifa, Israel.
Irina Libinson-ZebegretPediatric Nephrology Institute, Ruth Children's Hospital, Rambam Health Care Campus, Haifa, Israel.
Renata YakobovPediatric Nephrology Institute, Ruth Children's Hospital, Rambam Health Care Campus, Haifa, Israel.
Daniella MagenPediatric Nephrology Institute, Ruth Children's Hospital, Rambam Health Care Campus, Haifa, Israel.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Recurrent focal segmental glomerulosclerosis (rFSGS) is a severe condition occurring after kidney transplantation (KT) and has a high graft loss rate. Its incidence is reported as up to 55% of KTs, typically diagnosed within 1.5 months post-transplant. Treatment typically involves plasmapheresis, with adjunctive rituximab therapy, achieving partial or complete remission in up to 57% of patients. We report the case of a paediatric patient who experienced two episodes of rFSGS post-KT, presenting with acute kidney injury (AKI). The second episode was treated with subcutaneous ofatumumab with complete remission. Methods: The treatment protocol included four weekly plasmapheresis treatments, with Kesimpta administered subcutaneously at a dose of 20 mg twice weekly, given at the end of the plasmapheresis session. Plasmapheresis was then discontinued for 48-72 h following Kesimpta administration. CD20 levels were followed. Results: A KT patient experienced a second rFSGS, presenting with massive proteinuria of 13 g/day, 3 years post-transplant. Due to severe allergic reaction to rituximab during the first recurrence, she was treated with a combination of plasmapheresis and Kesimpta during the second episode. CD20 levels were undetected within two doses of Kesimpta treatment. Full remission and AKI resolved 1 month after initiation of this treatment. There were no severe adverse effects of the combined protocol. Conclusions: We propose a combination treatment of subcutaneous ofatumumab and intensive plasmapheresis, with CD19 and CD20 levels monitored regularly, might be safe and effective in rFSGS in KT patients.

Indexed as

kidney transplantofatumumabplasmapheresisrecurrent focal segmental glomerulosclerosistreatment protocol

Identifiers

PMID40212825
PMCPMC11982811

What Socratic holds

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LicenceCC BY-NC
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.