Evidence map›Paper›PMID 31487383›Full record

Trial reportThe British journal of dermatology2020

Rituximab is an effective treatment in patients with pemphigus vulgaris and demonstrates a steroid-sparing effect.

D M Chen, A Odueyungbo, E Csinady, L Gearhart, P Lehane, M Cheu, M Maho-Vaillant, C Prost-Squarcioni, V Hebert, E Houivet and 33 more

Open access · hybridAbstract readRandomized Controlled Trial
In one paragraph

Trial report in The British journal of dermatology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed, 3 pooled it
6.8field-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.

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, 3 syntheses or guidelines pooled it, 91 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Pooled it
  4. Trial
  5. Review
  6. Article
  7. Article
  8. Article
  9. Review
  10. Emerging Treatments in Pemphigus: Is Healing an Achievable Goal?American journal of clinical dermatology · 2026
    Review
  11. Article
  12. Bullous pemphigoid.Nature reviews. Disease primers · 2025
    Review
  13. Review
  14. Article
  15. Article
  16. Restoring immune tolerance in pemphigus vulgaris.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  17. Review
  18. Article
  19. Article
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

43 authors at 20 institutions in 4 countries.

D M ChenGenentech, Inc., South San Francisco, CA, U.S.A.
A OdueyungboRoche Products Ltd, Mississauga, ON, L5N 5M8, Canada.
E CsinadyF. Hoffmann-La Roche, Basel, Switzerland.
L GearhartF. Hoffmann-La Roche, Basel, Switzerland.
P LehaneRoche Products Ltd, Welwyn Garden City, AL7 1TW, U.K.
M CheuGenentech, Inc., South San Francisco, CA, U.S.A.
M Maho-VaillantDepartment of Dermatology, Rouen University Hospital and INSERM U 1234, National Reference Centre on Autoimmune Bullous Disease, Normandy University, 76000, Rouen, France.
C Prost-SquarcioniDepartment of Biostatistics, Rouen University Hospital and INSERM U1181, National Reference Centre on Autoimmune Bullous Disease, Normandy University, 76000, Rouen, France.
V HebertDepartment of Dermatology, Rouen University Hospital and INSERM U 1234, National Reference Centre on Autoimmune Bullous Disease, Normandy University, 76000, Rouen, France.
E HouivetDepartment of Dermatology, Avicenne Hospital and INSERM UMR1125, Paris 13 University, 93000, Bobigny, France.
S CalboDepartment of Dermatology, Rouen University Hospital and INSERM U 1234, National Reference Centre on Autoimmune Bullous Disease, Normandy University, 76000, Rouen, France.
F CaillotDepartment of Dermatology, Rouen University Hospital and INSERM U 1234, National Reference Centre on Autoimmune Bullous Disease, Normandy University, 76000, Rouen, France.
M L GolinskiDepartment of Dermatology, Rouen University Hospital and INSERM U 1234, National Reference Centre on Autoimmune Bullous Disease, Normandy University, 76000, Rouen, France.
B LabeilleDepartment of Dermatology, University of Saint Etienne, 42023, Saint Etienne, France.
C Picard-DahanDepartment of Dermatology, Bichat - Claude Bernard Hospital, 75018, Paris, France.
C PaulDepartment of Dermatology, University of Toulouse, 31013, Toulouse, France.
M A RichardDepartment of Dermatology, Assistance Publique des Hôpitaux de Marseille, Aix Marseille University, UMR 911, INSERM CRO2, 13007, Marseille, France.
J D BouazizDepartment of Dermatology of Saint Louis Hospital, Paris 7 Sorbonne Paris Cité University, 75010, Paris, France.
S Duvert-LehembreDepartment of Dermatology, Rouen University Hospital and INSERM U 1234, National Reference Centre on Autoimmune Bullous Disease, Normandy University, 76000, Rouen, France.
P BernardDepartment of Dermatology, University of Reims, 51100, Reims, France.
F CauxDepartment of Biostatistics, Rouen University Hospital and INSERM U1181, National Reference Centre on Autoimmune Bullous Disease, Normandy University, 76000, Rouen, France.
M AlexandreDepartment of Biostatistics, Rouen University Hospital and INSERM U1181, National Reference Centre on Autoimmune Bullous Disease, Normandy University, 76000, Rouen, France.
S Ingen-Housz-OroDepartment of Dermatology, APHP, Henri Mondor Hospital, 94010, Créteil, France.
P VabresDepartment of Dermatology, Dijon University Hospital, 21079, Dijon, France.
E DelaporteDepartment of Dermatology, University of Lille and Claude-Huriez Hospital, 59037, Lille, France.
G QuereuxDepartment of Dermatology, University of Nantes, 44035, Nantes, France.
A DupuyDepartment of Dermatology, University of Rennes, 35042, Rennes, France.
S DebarbieuxDepartment of Dermatology, Centre Hospitalier Lyon Sud, 69310, Pierre Bénite, France.
M Avenel-AudranDepartment of Dermatology, University of Angers, 49035, Angers, France.
M D'IncanDepartment of Dermatology, University of Clermont-Ferrand, 63001, Clermont-Ferrand, France.
C BedaneDepartment of Dermatology, University of Limoges, 87032, Limoges, France.
N BénétonDepartment of Dermatology, Le Mans General Hospital, 72037, Le Mans, France.
D JullienDepartment of Dermatology, Edouard Herriot Hospital, Lyon Claude Bernard University, 69003, Lyon, France.
N DupinDepartment of Dermatology, Cochin Hospital, University of Paris V, 75006, Paris, France.
L MiseryDepartment of Dermatology and, Brest University Hospital, 29200, Brest, France.
L MachetDepartment of Dermatology, Tours University Hospital, 37044, Tours, France.
M Beylot-BarryDepartment of Dermatology, University of Bordeaux, 33076, Bordeaux, France.
O DereureDepartment of Dermatology, University of Montpellier, 34090, Montpellier, France.
B SassolasDepartment of Internal Medicine, Brest University Hospital, 29200, Brest, France.
J BenichouDepartment of Dermatology, Avicenne Hospital and INSERM UMR1125, Paris 13 University, 93000, Bobigny, France.
P MusetteDepartment of Dermatology, Rouen University Hospital and INSERM U 1234, National Reference Centre on Autoimmune Bullous Disease, Normandy University, 76000, Rouen, France.
P JolyDepartment of Dermatology, Rouen University Hospital and INSERM U 1234, National Reference Centre on Autoimmune Bullous Disease, Normandy University, 76000, Rouen, France.
French Study Group on Autoimmune Bullous Diseases
Inserm · FRUniversité de Rouen Normandie · FRCentre Hospitalier Régional Universitaire de Brest · FRRoche (Switzerland) · CHUniversité Claude Bernard Lyon 1 · FRAix-Marseille Université · FRCentre Hospitalier du Mans · FRCentre Hospitalier Universitaire de Saint-Étienne · FRHôpital Cochin · FRHôpital Lyon Sud · FRMaison des Sciences de l’Homme de Dijon · FRNantes Université · FRRoche (Canada) · CARoche (United Kingdom) · GBSorbonne Paris Cité · FRUniversité Clermont Auvergne · FRUniversité d'Angers · FRUniversité de Bordeaux · FRUniversité de Lille · FRUniversité de Limoges · FR

Funding

Genentech
6 · The paper itself

Abstract

backgroundCorticosteroids (CS) with or without adjuvant immunosuppressant agents are standard treatment for pemphigus vulgaris (PV). The efficacy of adjuvant therapies in minimizing steroid-related adverse events (AEs) is unproven.

objectivesTo utilize data collected in a French investigator-initiated, phase III, open-label, randomized controlled trial to demonstrate the efficacy and safety of rituximab and seek approval for its use in PV.

methodsThis was an independently conducted post hoc analysis of the moderate-to-severe PV subset enrolled in the Ritux 3 study. Patients were randomized to rituximab plus 0·5 or 1·0 mg kg

resultsAt month 24, 34 of 38 patients (90%) on rituximab plus prednisone achieved CRoff ≥ 2 months vs. 10 of 36 patients (28%) on prednisone alone. Median total cumulative prednisone dose was 5800 mg in the rituximab plus prednisone arm vs. 20 520 mg for prednisone alone. Eight of 36 patients (22%) who received prednisone alone withdrew from treatment owing to AEs; one rituximab-plus-prednisone patient withdrew due to pregnancy. Overall, 24 of 36 patients (67%) on prednisone alone experienced a grade 3/4 CS-related AE vs. 13 of 38 patients (34%) on rituximab plus prednisone.

conclusionsIn patients with moderate-to-severe PV, rituximab plus short-term prednisone was more effective than prednisone alone. Patients treated with rituximab had less CS exposure and were less likely to experience severe or life-threatening CS-related AEs. What's already known about this topic? Pemphigus vulgaris (PV) is the most common type of pemphigus. Corticosteroids, a standard first-line treatment for PV, have significant side-effects. Although their effects are unproven, adjuvant corticosteroid-sparing agents are routinely used to minimize steroid exposure and corticosteroid-related side-effects. There is evidence that the anti-CD20 antibody rituximab is effective in the treatment of patients with severe recalcitrant pemphigus and in patients with newly diagnosed pemphigus. What does this study add? This study provides a more detailed analysis of patients with PV enrolled in an investigator-initiated trial. Rituximab plus prednisone had a steroid-sparing effect and more patients achieved complete remission off prednisone. Fewer patients experienced grade 3 or grade 4 steroid-related adverse events than those on prednisone alone. This collaboration between academia and industry, utilizing independent post hoc analyses, led to regulatory authority approvals of rituximab in moderate-to-severe PV.

Indexed as

PemphigusHumansImmunologic FactorsImmunosuppressive AgentsPrednisoneRituximabTreatment OutcomeImmunologic FactorsImmunosuppressive AgentsPrednisoneRituximab

Identifiers

PMID31487383
PMCPMC7317434
OpenAlexW2971900016

What OpenQuestion holds

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LicenceCC BY-NC-ND
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Registered trials

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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.