Evidence map›Paper›PMID 18465150›Full record

Trial reportPediatric nephrology (Berlin, Germany)2008

Rituximab treatment for severe steroid- or cyclosporine-dependent nephrotic syndrome: a multicentric series of 22 cases.

Vincent Guigonis, Aymeric Dallocchio, Véronique Baudouin, Maud Dehennault, Caroline Hachon-Le Camus, Mickael Afanetti, Jaap Groothoff, Brigitte Llanas, Patrick Niaudet, Hubert Nivet and 4 more

Registry-linked trialAbstract readClinical TrialMulticenter Study
PubMed Publisher
In one paragraph

Trial report in Pediatric nephrology (Berlin, Germany), 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT04494438 (Rituximab in Patients With Low Dose Steroid-dependent Idiopathic Nephrotic Syndrome), which is not on this map. Cited by 123 papers, 5 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
123citing papers in PubMed, 5 pooled it
11.2field-weighted citation impact, top 1% 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.

NCT04494438 phase3completednot on this mapstarted 2013, after this paper: background citation

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

TypeinterventionalSponsorIstituto Giannina GasliniRan2013 to 2016Enrolled30ConditionsIdiopathic Nephrotic SyndromeArmsRituximab
3 · Its place in the literature

Who cites it

123 citing papers in PubMed, 5 syntheses or guidelines pooled it, 248 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Pooled it
  4. Guideline
  5. Guideline
  6. Trial
  7. Trial
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  12. Rituximab in children with resistant idiopathic nephrotic syndrome.Journal of the American Society of Nephrology : JASN · 2012
    Trial
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  15. Rituximab for refractory cases of childhood nephrotic syndrome.Pediatric nephrology (Berlin, Germany) · 2011
    Trial
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  17. Trial
  18. Review
  19. Observational
  20. Article

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

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

14 authors at 11 institutions in 2 countries.

Vincent GuigonisDepartment of Pediatrics, Centre de référence des maladies rénales rares du Sud-Ouest, Hôpital de la mère et de l'enfant, 8 Ave Dominique Larrey, 87000 Limoges, France. vincent.guigonis@chu-limoges.fr
Aymeric Dallocchio
Véronique Baudouin
Maud Dehennault
Caroline Hachon-Le Camus
Mickael Afanetti
Jaap Groothoff
Brigitte Llanas
Patrick Niaudet
Hubert Nivet
Natacha Raynaud
Sophie Taque
Pierre Ronco
François Bouissou
Hôpital Mère-Enfant · FRHôpital Purpan · FRAssistance Publique – Hôpitaux de Paris · FRCentre Hospitalier Universitaire de Tours · FREmma Kinderziekenhuis · NLHôpital Jeanne de Flandre · FRHôpital l'Archet · FRHôpital Necker-Enfants Malades · FRHôpital Pellegrin · FRHôpital Pontchaillou · FRSorbonne Université · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Several case reports suggest that rituximab (RTX) could be effective in steroid-dependent nephrotic syndrome, but RTX efficacy has not yet been studied in a series of patients. Safety and efficacy of RTX were assessed in a multicenter series of 22 patients aged 6.3-22 years with severe steroid-dependent nephrotic syndrome or steroid-resistant but cyclosporin-sensitive idiopathic nephrotic syndrome. Patients were treated with two to four infusions of RTX. Seven patients were nephrotic at the time of RTX treatment. Peripheral B cells were depleted in all subjects. Remission was induced in three of the seven proteinuric patients. One or more immunosuppressive (IS) treatments could be withdrawn in 19 patients (85%), with no relapse of proteinuria and without increasing other IS drugs. RTX was effective in all patients when administered during a proteinuria-free period in association with other IS agents. When relapses occurred, they were always associated with an increase in CD19 cell count. Adverse effects were observed in 45% of cases, but most of them were mild and transient. This study suggests that RTX could be an effective treatment for severe steroid-dependent nephrotic syndrome.

Indexed as

AdultAntibodies, MonoclonalAntibodies, Monoclonal, Murine-DerivedAntigens, CD19B-LymphocytesChildChild, PreschoolCyclosporineDrug Therapy, CombinationFemaleHumansImmunologic FactorsImmunosuppressive AgentsInfantMaleNephrotic SyndromeAntibodies, MonoclonalAntibodies, Monoclonal, Murine-DerivedAntigens, CD19CyclosporineImmunologic FactorsImmunosuppressive AgentsRituximabSteroids

Identifiers

PMID18465150
OpenAlexW2003607385

What OpenQuestion holds

Textmetadata
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.