Evidence map›Paper›PMID 38983857›Full record

ArticleFrontiers in immunology2024

Activity of apremilast in a patient with severe pemphigus vulgaris: case report.

Cheyenne Delvaux, Gérôme Bohelay, Ishaï-Yaacov Sitbon, Isaac Soued, Marina Alexandre, Joël Cucherousset, Laurent Gilardin, Antoine Diep, Frédéric Caux, Christelle Le Roux-Villet

Abstract readCase Reports
In one paragraph

Article in Frontiers in immunology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
–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

7 citing papers in PubMed.

  1. Review
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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

10 authors.

Cheyenne DelvauxDepartment of Dermatology, Saint-Pierre and Brugmann University Hospitals, Université Libre de Bruxelles, Brussels, Belgium.
Gérôme BohelayDepartment of Dermatology and Referral Center for Autoimmune Bullous Diseases MALIBUL, Avicenne Hospital, AP-HP, Sorbonne Paris Nord University, Bobigny, France.
Ishaï-Yaacov SitbonDepartment of Dermatology and Referral Center for Autoimmune Bullous Diseases MALIBUL, Avicenne Hospital, AP-HP, Sorbonne Paris Nord University, Bobigny, France.
Isaac SouedDepartment of ENT, Avicenne Hospital AP-HP, Sorbonne Paris Nord University, Bobigny, France.
Marina AlexandreDepartment of Dermatology and Referral Center for Autoimmune Bullous Diseases MALIBUL, Avicenne Hospital, AP-HP, Sorbonne Paris Nord University, Bobigny, France.
Joël CucheroussetDepartment of Pathology, Avicenne Hospital AP-HP, Sorbonne Paris Nord University, Bobigny, France.
Laurent GilardinDepartment of Internal Medicine, Jean-Verdier Hospital, Bondy, France.
Antoine DiepDepartment of Immunology, Saint-Louis Hospital, Paris, France.
Frédéric CauxDepartment of Dermatology and Referral Center for Autoimmune Bullous Diseases MALIBUL, Avicenne Hospital, AP-HP, Sorbonne Paris Nord University, Bobigny, France.
Christelle Le Roux-VilletDepartment of Dermatology and Referral Center for Autoimmune Bullous Diseases MALIBUL, Avicenne Hospital, AP-HP, Sorbonne Paris Nord University, Bobigny, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Although the treatment for pemphigus vulgaris (PV) has been revolutionized by the use of rituximab combined with corticosteroids, new effective therapies with a better safety profile are needed. Observation: A 67-year-old woman was diagnosed with severe mucosal PV, which was initially misdiagnosed as atypical Behçet's disease. Following an unsuccessful colchicine treatment, significant improvement was observed upon the introduction of apremilast: reduced pain, fewer lesions, and a stabilized weight. The discontinuation of apremilast led to a rapid relapse. Retrospective analysis through anti-Dsg3 ELISA indicated a gradual decrease in antibody levels during the apremilast treatment. Discussion: Apremilast, a phosphodiesterase 4 inhibitor approved for psoriasis and Behçet's disease's related oral ulcers treatment, demonstrated its efficacy in this PV case. This is the second case report highlighting the effectiveness of apremilast for PV treatment. Apremilast's ability to upregulate cyclic adenosine monophosphate (cAMP) levels appears to contribute to the stabilization of keratinocyte adhesion. Conclusion: Apremilast may be a promising therapeutic option for the treatment of pemphigus, with an innovative mechanism of action, no induced immunosuppression, and good tolerance. It could be a good alternative to steroids, in the treatment regimen of steroids combined with rituximab.

Indexed as

PemphigusThalidomideAgedAnti-Inflammatory Agents, Non-SteroidalFemaleHumansPhosphodiesterase 4 InhibitorsTreatment OutcomeAnti-Inflammatory Agents, Non-SteroidalapremilastPhosphodiesterase 4 InhibitorsThalidomideapremilastauto-immune bullous diseasekeratinocytespemphigus vulgarisphosphodiesterase 4 inhibitor

Identifiers

PMID38983857
PMCPMC11231183

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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.