Evidence map›Paper›PMID 28915275›Full record

Trial reportPloS one2017

Long-term efficacy and safety of rituximab in IgG4-related disease: Data from a French nationwide study of thirty-three patients.

Mikael Ebbo, Aurélie Grados, Maxime Samson, Matthieu Groh, Anderson Loundou, Aude Rigolet, Benjamin Terrier, Constance Guillaud, Clarisse Carra-Dallière, Frédéric Renou and 19 more

Abstract readClinical TrialMulticenter Study
In one paragraph

Trial report in PloS one, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 100 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
100citing papers in PubMed, 2 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

100 citing papers in PubMed, 2 syntheses or guidelines pooled it.

  1. Pooled it
  2. Immunoglobulin G4-related hypertrophic pachymeningitis: A case-oriented review.Neurology(R) neuroimmunology & neuroinflammation · 2019
    Pooled it
  3. Review
  4. Article
  5. Article
  6. Management of IgG4-Related Disease.Current rheumatology reports · 2026
    Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Review
  17. Article
  18. Review
  19. Immunosuppressants for IgG4-related disease.The Cochrane database of systematic reviews · 2025
    Article
  20. Article

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

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

29 authors.

Mikael EbboDepartment of Internal Medicine, Hôpital de la Timone, AP-HM, Aix-Marseille Université, Marseille, France.ORCID http://orcid.org/0000-0002-1179-8113
Aurélie GradosDepartment of Internal Medicine, Hôpital de la Timone, AP-HM, Aix-Marseille Université, Marseille, France.
Maxime SamsonDepartment of Internal Medicine and Clinical Immunology, Dijon University Hospital, Dijon, France.
Matthieu GrohDepartment of Internal Medicine, Hôpital Cochin, AP-HP, Centre National de Référence Maladies Systémiques et Auto-immunes Rares, Université René-Descartes Paris V, Sorbonne Paris Cité, Paris, France.
Anderson LoundouUnité d'Aide Méthodologique, Aix-Marseille Université, AP-HM, Marseille, France.
Aude RigoletDepartment of Internal Medicine and Clinical Immunology, AP-HP, Hôpital La Pitié-Salpêtrière; DHUI2B, Université Pierre et Marie Curie Paris VI, Paris, France.
Benjamin TerrierDepartment of Internal Medicine, Hôpital Cochin, AP-HP, Centre National de Référence Maladies Systémiques et Auto-immunes Rares, Université René-Descartes Paris V, Sorbonne Paris Cité, Paris, France.
Constance GuillaudDepartment of Internal Medicine, Hôpital Henri Mondor, AP-HP, Créteil, France.
Clarisse Carra-DallièreDepartment of Neurology, CHRU de Montpellier, Montpellier, France.
Frédéric RenouDepartment of Internal Medicine, CHU La Réunion site Félix Guyon, Saint-Denis, La Réunion, France.
Agnieszka PozdzikDepartment of Nephrology, Erasme Hospital, Cliniques Universitaires de Bruxelles, Bruxelles, Belgium.
Pierre LabaugeDepartment of Neurology, CHRU de Montpellier, Montpellier, France.
Sylvain PalatDepartment of Internal Medicine, CHU Limoges, Limoges, France.
Jean-Marie BerthelotDepartment of Rheumatology, CHU Nantes, Nantes, France.
Jean-Loup PennaforteDepartment of Internal Medicine, CHU de Reims, Reims, France.
Alain WynckelDepartment of Nephrology, CHU de Reims, Reims, France.
Céline LebasDepartment of Nephrology, CHRU de Lille, Lille, France.
Noémie Le GouellecDepartment of Nephrology and Internal Medicine, CH Valenciennes, Valenciennes, France.
Thomas QuémeneurDepartment of Nephrology and Internal Medicine, CH Valenciennes, Valenciennes, France.
Karine DahanDepartment of Nephrology, Hôpital Tenon, AP-HP, Paris, France.
Franck CarbonnelDepartment of Gastro-enterology, CHU Bicêtre, Le Kremlin Bicêtre, France.
Gaëlle LerouxDepartment of Internal Medicine and Clinical Immunology, AP-HP, Hôpital La Pitié-Salpêtrière; DHUI2B, Université Pierre et Marie Curie Paris VI, Paris, France.
Antoinette PerlatDepartment of Internal Medicine, Hôpital Sud, CHU de Rennes, Rennes, France.
Alexis MathianDepartment of Internal Medicine, Hôpital Pitié-Salpêtrière, AP-HP, Centre National de Référence Maladies Systémiques et Auto-immunes Rares, Université Pierre et Marie Curie Paris VI, Paris, France.
Patrice CacoubDepartment of Internal Medicine and Clinical Immunology, AP-HP, Hôpital La Pitié-Salpêtrière; DHUI2B, Université Pierre et Marie Curie Paris VI, Paris, France.
Eric HachullaNational Referral Centre for Auto-immune and Systemic Diseases, Department of Internal Medicine, Huriez Hospital, Université de Lille, Lille, France.
Nathalie Costedoat-ChalumeauDepartment of Internal Medicine, Hôpital Cochin, AP-HP, Centre National de Référence Maladies Systémiques et Auto-immunes Rares, Université René-Descartes Paris V, Sorbonne Paris Cité, Paris, France.
Jean-Robert HarléDepartment of Internal Medicine, Hôpital de la Timone, AP-HM, Aix-Marseille Université, Marseille, France.
Nicolas SchleinitzDepartment of Internal Medicine, Hôpital de la Timone, AP-HM, Aix-Marseille Université, Marseille, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesTo assess efficacy and safety of rituximab (RTX) as induction therapy, maintenance of remission and treatment of relapses in a cohort of IgG4-related disease (IgG4-RD) patients.

methodsNationwide retrospective multicenter study of IgG4-RD patients treated with at least one course of RTX. Clinical, biological and radiological response, relapse rate and drug tolerance were analyzed. Kaplan-Meier curves were plotted and risk factors for relapse studied with a Cox regression model.

resultsAmong 156 IgG4-RD patients included in the French database, 33 received rituximab. Clinical response was noted in 29/31 (93.5%) symptomatic patients. Glucocorticoids withdrawal was achieved in 17 (51.5%) patients. During a mean follow-up of 24.8 ±21 months, 13/31 (41.9%) responder patients relapsed after a mean delay of 19 ±11 months after RTX. Active disease, as defined by an IgG4-RD Responder Index >9 before RTX, was significantly associated with relapse (HR = 3.68, 95% CI: 1.1, 12.6) (P = 0.04), whereas maintenance therapy with systematic (i.e. before occurrence of a relapse) RTX retreatment was associated with longer relapse-free survival (41 versus 21 months; P = 0.02). Eight severe infections occurred in 4 patients during follow-up (severe infections rate of 12.1/100 patient-years) and hypogammaglobulinemia ≤5 g/l in 3 patients.

conclusionRTX is effective for both induction therapy and treatment of relapses in IgG4-RD, but relapses are frequent after B-cell reconstitution. Maintenance therapy with systematic RTX infusions is associated with longer relapse-free survival and might represent a novel treatment strategy. Yet, the high rate of infections and the temporary effect of RTX might be hindrances to such strategy.

Indexed as

Databases, FactualAgedAutoimmune DiseasesFemaleFollow-Up StudiesFranceHumansImmunoglobulin GMaleMiddle AgedRituximabImmunoglobulin GRituximab

Identifiers

PMID28915275
PMCPMC5600376

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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.