Evidence map›Paper›PMID 29436729›Full record

ArticleBritish journal of clinical pharmacology2018

Adverse events linked with the use of chimeric and humanized anti-CD20 antibodies in children with idiopathic nephrotic syndrome.

Alice Bonanni, Marta Calatroni, Matteo D'Alessandro, Sara Signa, Enrica Bertelli, Michela Cioni, Eddi Di Marco, Roberto Biassoni, Gianluca Caridi, Giulia Ingrasciotta and 7 more

Open access · bronzeAbstract read
In one paragraph

Article in British journal of clinical pharmacology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed, 2 pooled it
5.6field-weighted citation impact, top 3% 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.

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

37 citing papers in PubMed, 2 syntheses or guidelines pooled it, 55 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Trial
  4. Trial
  5. Article
  6. Article
  7. Article
  8. Review
  9. Article
  10. Review
  11. [Clinical study on low-dose rituximab maintenance therapy in children with primary nephrotic syndrome].Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics · 2025
    Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Precision medicine for focal segmental glomerulosclerosis.Kidney research and clinical practice · 2024
    Article
  17. Article
  18. Article
  19. Article
  20. Update on the treatment of steroid-sensitive nephrotic syndrome.Pediatric nephrology (Berlin, Germany) · 2022
    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

17 authors at 3 institutions in 2 countries.

Alice BonanniDivision of Nephrology, Dialysis, Transplantation, IRCCS Giannina Gaslini, Via Gerolamo Gaslini 5, Genoa, 16148, Italy.
Marta CalatroniDialysis and Transplantation Policlinico IRCCS Fondazione San Matteo and University of Pavia, Pavia, Italy.
Matteo D'AlessandroDivision of Nephrology, Dialysis, Transplantation, IRCCS Giannina Gaslini, Via Gerolamo Gaslini 5, Genoa, 16148, Italy.
Sara SignaDivision of Nephrology, Dialysis, Transplantation, IRCCS Giannina Gaslini, Via Gerolamo Gaslini 5, Genoa, 16148, Italy.
Enrica BertelliDivision of Nephrology, Dialysis, Transplantation, IRCCS Giannina Gaslini, Via Gerolamo Gaslini 5, Genoa, 16148, Italy.
Michela CioniLaboratory of Molecular Nephrology, IRCCS Giannina Gaslini, Genoa, Italy.
Eddi Di MarcoDepartment of Translational Medicine, Istituto Giannina Gaslini, Largo G. Gaslini 5, Genoa, 16147, Italy.
Roberto BiassoniDepartment of Translational Medicine, Istituto Giannina Gaslini, Largo G. Gaslini 5, Genoa, 16147, Italy.
Gianluca CaridiLaboratory of Molecular Nephrology, IRCCS Giannina Gaslini, Genoa, Italy.
Giulia IngrasciottaDivision of Nephrology, Dialysis, Transplantation, IRCCS Giannina Gaslini, Via Gerolamo Gaslini 5, Genoa, 16148, Italy.
Roberta BertelliLaboratory of Molecular Nephrology, IRCCS Giannina Gaslini, Genoa, Italy.
Armando Di DonatoLaboratory of Molecular Nephrology, IRCCS Giannina Gaslini, Genoa, Italy.
Maurizio BruschiLaboratory of Molecular Nephrology, IRCCS Giannina Gaslini, Genoa, Italy.
Alberto CanepaDivision of Nephrology, Dialysis, Transplantation, IRCCS Giannina Gaslini, Via Gerolamo Gaslini 5, Genoa, 16148, Italy.
Giorgio PiaggioDivision of Nephrology, Dialysis, Transplantation, IRCCS Giannina Gaslini, Via Gerolamo Gaslini 5, Genoa, 16148, Italy.
Pietro RavaniDivision of Nephrology, University of Calgary, 1403-29th Street NW, Calgary, AB, T2N 2T9, Canada.
Gian Marco GhiggeriDivision of Nephrology, Dialysis, Transplantation, IRCCS Giannina Gaslini, Via Gerolamo Gaslini 5, Genoa, 16148, Italy.ORCID 0000-0003-3659-9062
Istituto Giannina Gaslini · ITUniversity of Calgary · CAUniversity of Pavia · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimsAnti-CD20 antibodies are increasingly being used to treat idiopathic nephrotic syndrome (INS) in children. While they may allow steroid and calcineurin inhibitor withdrawal, repeated infusions of anti-CD20 antibodies are often required to maintain remission. Data on their potential toxicity in INS are needed, to consider repeated infusions.

methodsWe investigated the side effects associated with the use of rituximab (a chimeric antibody; 130 patients) and ofatumumab (a humanized antibody; 37 patients) in children with INS (steroid-dependent and steroid/calcineurin inhibitor-dependent disease) treated at a national referral centre over a 9-year period (400 treatments; follow-up 1-9 years).

resultsInfusion reactions were mainly absent in children with steroid-dependent disease. Rash, dyspnoea, fever, cough and itchy throat (5% and 18% following rituximab and ofatumumab infusion, respectively) were resolved by using premedication with salbutamol. Other short-term reactions (up to 3 months), including arthritis (2%) and lung injury (1%), were more common with rituximab. Infections were observed 3-9 months following infusion, were similarly common in the two groups and resolved with targeted therapies [antibiotic, fluconazole, immunoglobulins (Igs), etc.]. The number of circulating CD19/20 cells fell to 0 at month 1 and were reconstituted at month 3; circulating IgG antibodies remained within the normal range for 1 year. Tetanus and hepatitis B virus immunization was not modified by either treatment; Epstein-Barr virus and John Cunningham virus activation markers were occasionally observed.

conclusionOverall, the toxicity of anti-CD20 monoclonal antibodies was limited to post-infusion side effects in children with more complex disease. The relatively safe profile of anti-CD20 antibodies supports their use as steroid-sparing agents in children with INS.

Indexed as

AdolescentAge FactorsAntibodies, MonoclonalAntibodies, Monoclonal, HumanizedAntigens, CD20ChildChild, PreschoolFemaleHumansImmunologic FactorsInfusions, IntravenousMaleNephrotic SyndromePatient SafetyRisk AssessmentRisk FactorsAntibodies, MonoclonalAntibodies, Monoclonal, HumanizedAntigens, CD20Immunologic FactorsofatumumabRituximabnephrotic syndromeofatumumabrituximabside effects

Identifiers

PMID29436729
PMCPMC5980330
OpenAlexW2792085519

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.