Evidence map›Paper›PMID 41863638›Full record

ArticlePediatric nephrology (Berlin, Germany)2026

B cell depletion with rituximab in children with steroid-sensitive nephrotic syndrome: does depletion duration change outcome?

Gael Cals, Claire Dossier, Olivia Boyer, Jean Daniel Delbet, Julien Hogan, Antoine Mouche, Tim Ulinski, Cyrielle Parmentier

Abstract readMulticenter Study
PubMed Publisher
In one paragraph

Article in Pediatric nephrology (Berlin, Germany), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
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

8 authors.

Gael CalsPediatric Nephrology Unit-Trousseau Hospital-APHP, ORIGYNE and Sorbonne University, 26 Avenue du Docteur Arnold Netter, 75012, Paris, France.
Claire DossierPediatric Nephrology Unit-Robert Debré Hospital-APHP, University-Paris Cité, Paris, France.
Olivia BoyerPediatric Nephrology Unit-Necker Enfants Malades-APHP, Reference Center for Idiopathic Nephrotic Syndrome in Children and Adults, Imagine Institute, University-Paris Cité, Paris, France.
Jean Daniel DelbetPediatric Nephrology Unit-Trousseau Hospital-APHP, ORIGYNE and Sorbonne University, 26 Avenue du Docteur Arnold Netter, 75012, Paris, France.
Julien HoganPediatric Nephrology Unit-Robert Debré Hospital-APHP, University-Paris Cité, Paris, France.
Antoine MouchePediatric Nephrology Unit-Trousseau Hospital-APHP, ORIGYNE and Sorbonne University, 26 Avenue du Docteur Arnold Netter, 75012, Paris, France.
Tim UlinskiPediatric Nephrology Unit-Trousseau Hospital-APHP, ORIGYNE and Sorbonne University, 26 Avenue du Docteur Arnold Netter, 75012, Paris, France.
Cyrielle ParmentierPediatric Nephrology Unit-Trousseau Hospital-APHP, ORIGYNE and Sorbonne University, 26 Avenue du Docteur Arnold Netter, 75012, Paris, France. cyrielle.parmentier@aphp.fr.ORCID http://orcid.org/0000-0002-3849-2659

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundRituximab (RTX) is widely used to prevent relapses in steroid-dependent or frequently-relapsing nephrotic syndrome (SD/FRNS). However, the impact of B-cell depletion duration on long-term outcomes remains uncertain. We compared short-term B-cell depletion (limited RTX course) with prolonged depletion maintained by repeated RTX infusions and assessed long-term disease activity.

methodsIn this retrospective multicenter study, we included children with SD/FRNS who received RTX before the age of 18 years between 2007 and 2017. Short-depletion corresponded to one or two RTX infusions, whereas prolonged-depletion reflected repeated infusions over time to maintain B-cell depletion. Prolonged remission was defined as the absence of relapse and immunosuppressive therapy for at least 2 years after the last anti-CD20 infusion.

resultsA total of 117 patients were included (median age at first RTX infusion: 11.6 years; 65% were boys), of whom 48 (41%) had short-depletion and 69 (59%) had prolonged-depletion. Baseline characteristics were comparable between groups. At 2 years after the last RTX infusion, 69% of patients in the short-depletion group and 65% in the prolonged-depletion group were in prolonged remission. Overall, 89 patients (75%) relapsed during follow-up. Median time to first relapse was significantly longer in the long-depletion group (36 vs. 19 months, p = 0.04). Prolonged hypogammaglobulinemia was more frequent with prolonged-depletion, whereas infection rates were similar between groups.

conclusionRTX exerts a suspensive rather than curative effect in SD/FRNS. Prolonged B-cell depletion extends relapse-free survival but is associated with more frequent hypogammaglobulinemia, without an increase in severe infections.

Indexed as

B-LymphocytesImmunologic FactorsLymphocyte DepletionNephrotic SyndromeRituximabAdolescentChildChild, PreschoolFemaleHumansImmunosuppressive AgentsMaleRecurrenceRemission InductionRetrospective StudiesSecondary PreventionImmunologic FactorsImmunosuppressive AgentsRituximabB-cell depletionHypogammaglobulinemiaPediatricRituximabSteroid-sensitive nephrotic syndrome

Identifiers

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.