Evidence map›Paper›PMID 23739238›Full record

ArticleKidney international2013

Rituximab is a safe and effective long-term treatment for children with steroid and calcineurin inhibitor-dependent idiopathic nephrotic syndrome.

Pietro Ravani, Alessandro Ponticelli, Chiara Siciliano, Alessia Fornoni, Alberto Magnasco, Felice Sica, Monica Bodria, Gianluca Caridi, Changli Wei, Mirco Belingheri and 14 more

4 registry-linked trialsOpen access · bronzeAbstract read
In one paragraph

Article in Kidney international, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 4 registered trials, which are not on this map. Cited by 77 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
77citing papers in PubMed, 1 pooled it
8.1field-weighted citation impact, top 2% of its field
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.

NCT02394119 phase2completednot on this mapstarted 2015, after this paper: background citation

Ofatumumab Versus Rituximab in Children With Steroid and Calcineurin Inhibitor-dependent Idiopathic Nephrotic Syndrome: an Open-label, Randomized, Controlled, Superiority Trial.

TypeinterventionalSponsorIstituto Giannina GasliniRan2015 to 2019Enrolled140ConditionsNephrotic SyndromeArmsOfatumumab, Rituximab
NCT02455908 phase1 / phase2completednot on this map

Use of IL-2 for Pediatric, Multi Drug Resistant, Idiopathic Nephrotic Syndrome

TypeinterventionalSponsorIstituto Giannina GasliniRan2012 to 2012Enrolled5ConditionsNephrotic SyndromeArmsProleukin®
NCT04494438 phase3completednot on this map

Rituximab in Patients With Low Dose Steroid-dependent Idiopathic Nephrotic Syndrome

TypeinterventionalSponsorIstituto Giannina GasliniRan2013 to 2016Enrolled30ConditionsIdiopathic Nephrotic SyndromeArmsRituximab
NCT05734794 phase3unknown statusnot on this mapstarted 2023, after this paper: background citation

Study of Rituximab Monotherapy VS Steroid Therapy on Children With New-onset Nephrotic Syndrome: A Randomized Controlled Trial

TypeinterventionalSponsorThe Children's Hospital of Zhejiang University School of MedicineRan2023 to 2026Enrolled80ConditionsNephrotic Syndrome in Children, RituximabArmsRituximab, Steroid
3 · Its place in the literature

Who cites it

77 citing papers in PubMed, 1 synthesis or guideline pooled it, 128 citations in OpenAlex.

  1. Pooled it
  2. Steroid-sparing drugs in children and young adults with nephrotic syndrome: a target trial emulation.Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association · 2026
    Trial
  3. Trial
  4. Trial
  5. Trial
  6. Trial
  7. Trial
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  9. Trial
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  12. Rituximab in steroid-dependent or frequently relapsing idiopathic nephrotic syndrome.Journal of the American Society of Nephrology : JASN · 2014
    Trial
  13. Article
  14. Article
  15. Review
  16. Article
  17. [Efficacy and safety of rituximab in children with refractory nephrotic syndrome].Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics · 2026
    Article
  18. Review
  19. Article
  20. Review

17 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

24 authors at 8 institutions in 3 countries.

Pietro RavaniDivision of Nephrology, Department of Medicine, Faculty of Medicine, University of Calgary, Calgary, Alberta, Canada.
Alessandro Ponticelli
Chiara Siciliano
Alessia Fornoni
Alberto Magnasco
Felice Sica
Monica Bodria
Gianluca Caridi
Changli Wei
Mirco Belingheri
Luciana Ghio
Sandra Merscher-Gomez
Alberto Edefonti
Andrea Pasini
Giovanni Montini
Corrado Murtas
Xiangyu Wang
Daniel Muruve
Augusto Vaglio
Davide Martorana
Antonello Pani
Francesco Scolari
Jochen Reiser
Gian M Ghiggeri
Istituto Giannina Gaslini · ITFondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico · ITUniversity of Calgary · CAUniversity of Miami · USOspedale di Parma · ITAzienda Ospedaliera G. Brotzu · ITRush University · USUniversity of Foggia · IT

Funding

Novel Targets of Rituximab in FSGSR01DK090316 · NIDDK · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI FORNONI, ALESSIA · 2011 to 2015
$1.7M
NIDDK NIH HHS R01 DK090316
6 · The paper itself

Abstract

In children with idiopathic nephrotic syndrome, rituximab can maintain short-term remission with withdrawal of prednisone and calcineurin inhibitors. Long-term effects including the number of repeated infusions to maintain remission are unknown. To test this, we treated 46 consecutive children with idiopathic nephrotic syndrome lasting for at least 1 year (mean 6.3 years), maintained in remission with oral prednisone and calcineurin inhibitors. They received 1-5 rituximab courses during a median follow-up of 3 years. Oral agents were tapered after each infusion, and completely withdrawn within 45 days. Rituximab was well tolerated. Six-month probabilities of remission were 48% after the first infusion and 37% after subsequent infusions. One- and 2-year-remission probabilities were, respectively, 20 and 10%. Median time intervals between complete oral-agent withdrawal and relapse were 5.6 and 8.5 months, respectively, following the first and subsequent courses. The time to reconstitution of CD20 cells correlated with the duration of remission, but was not associated with variation in FcyR, CD20, or SMPDL-3B polymorphisms. Podocyte Src phosphorylation was normal. Thus, rituximab can be safely and repeatedly used as a prednisone and calcineurin inhibitor-sparing therapy in a considerable proportion of children with dependent forms of idiopathic nephrotic syndrome. Further study is needed to identify patients who will benefit most from rituximab therapy.

Indexed as

Calcineurin InhibitorsAdministration, OralAdolescentAge FactorsAntibodies, Monoclonal, Murine-DerivedAntigens, CD20CalcineurinChildChild, PreschoolDrug Administration ScheduleFemaleGlucocorticoidsHumansImmunosuppressive AgentsInfusions, IntravenousKaplan-Meier EstimateAntibodies, Monoclonal, Murine-DerivedAntigens, CD20CalcineurinCalcineurin InhibitorsFCGR2B protein, humanFCGR3A protein, humanGlucocorticoidsImmunosuppressive AgentsPrednisoneReceptors, IgGRituximabSMPDL3B protein, humanSphingomyelin Phosphodiesterasesrc-Family Kinases

Identifiers

PMID23739238
PMCPMC3816123
OpenAlexW2076316204

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

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.