Evidence map›Paper›PMID 27687621›Full record

ArticlePediatric nephrology (Berlin, Germany)2017

Ofatumumab in two pediatric nephrotic syndrome patients allergic to rituximab.

Marina Vivarelli, Manuela Colucci, Alice Bonanni, Martina Verzani, Jessica Serafinelli, Francesco Emma, Gianmarco Ghiggeri

Abstract readCase Reports
PubMed Publisher
In one paragraph

Article in Pediatric nephrology (Berlin, Germany), 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed, 1 pooled it
–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

25 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Guideline
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  7. Article
  8. B-cell Depletion Therapy in Pediatric Neuroinflammatory Disease.Current neurology and neuroscience reports · 2024
    Review
  9. Review
  10. Review
  11. Update on the treatment of steroid-sensitive nephrotic syndrome.Pediatric nephrology (Berlin, Germany) · 2022
    Review
  12. Review
  13. Article
  14. Review
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  16. Article
  17. Article
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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

7 authors.

Marina VivarelliDivision of Nephrology and Dialysis, IRCCS-Bambino Gesù Children's Hospital, Rome, Italy. marina.vivarelli@opbg.net.
Manuela ColucciDivision of Nephrology and Dialysis, IRCCS-Bambino Gesù Children's Hospital, Rome, Italy.
Alice BonanniDivision of Nephrology, Dialysis, and Transplantation, IRCCS-Istituto Giannina Gaslini, Genoa, Italy.
Martina VerzaniDivision of Nephrology and Dialysis, IRCCS-Bambino Gesù Children's Hospital, Rome, Italy.
Jessica SerafinelliDivision of Nephrology and Dialysis, IRCCS-Bambino Gesù Children's Hospital, Rome, Italy.
Francesco EmmaDivision of Nephrology and Dialysis, IRCCS-Bambino Gesù Children's Hospital, Rome, Italy.
Gianmarco GhiggeriDivision of Nephrology, Dialysis, and Transplantation, IRCCS-Istituto Giannina Gaslini, Genoa, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundRituximab, a chimeric anti-CD20 monoclonal antibody, is an effective treatment in steroid-dependent nephrotic syndrome (SDNS). However, some patients develop adverse reactions. CASE-DIAGNOSIS/TREATMENT: Patient 1, a 14-year-old boy with SDNS since the age of 2, was treated with oral prednisone, cyclosporine A (CsA) and mycophenolate mofetil. A first infusion of rituximab at age 12 years was well tolerated, but this was followed by a prolonged relapse unresponsive to oral prednisone, mycophenolate mofetil and CsA. A second rituximab infusion was attempted, but treatment was interrupted due to severe dyspnea. Treatment with a humanized anti-CD20 monoclonal antibody, ofatumumab, was then attempted. The patient experienced a mild allergic reaction and maintained remission despite interruption of all treatment at >12 months of follow-up. Patient 2, a 3-year-old boy who presented at 18 months with nephrotic syndrome initially resistant to treatment with oral prednisone, was given with three intravenous boluses of methylprednisolone followed by CsA and achieved remission. Upon steroid discontinuation, the NS relapsed. Prednisone was restarted and treatment with a single dose of rituximab was never completed due to a severe allergic reaction. Ofatumumab infusion was uneventful, and he maintained remission during the follow-up period (>12 months) despite interruption of prednisone therapy. B cells reappeared at 7 months in both patients.

conclusionsOfatumumab may be a therapeutic option in severe forms of NS with allergy to rituximab.

Indexed as

Drug HypersensitivityAdolescentAntibodies, MonoclonalAntibodies, Monoclonal, HumanizedAnti-Inflammatory AgentsB-LymphocytesChild, PreschoolCyclosporineDrug ResistanceHumansImmunosuppressive AgentsMaleMethylprednisoloneMycophenolic AcidNephrotic SyndromePrednisoneAntibodies, MonoclonalAntibodies, Monoclonal, HumanizedAnti-Inflammatory AgentsCyclosporineImmunosuppressive AgentsMethylprednisoloneMycophenolic AcidofatumumabPrednisoneRituximabAdverse reactionChildrenOfatumumabRituximabSteroid-dependent nephrotic syndromeSteroid-resistant nephrotic syndrome

Identifiers

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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 OpenQuestion graph.