Evidence map›Paper›PMID 41626198›Full record

ArticleFrontiers in allergy2025

Case Series: Combination of dupilumab and omalizumab as a way to reduce dupilumab-associated adverse events in severe atopic dermatitis.

Daria S Fomina, Olga A Mukhina, Elizaveta L Sedova, Marina S Lebedkina, Elena N Bobrikova, Alexander V Karaulov, Mariana A Lysenko, Harald Renz

Abstract readCase Reports
In one paragraph

Article in Frontiers in allergy, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Revisiting Atopy: The IgE-Dependent Amplification Loop as a Forgotten Driver of Atopic Dermatitis.Pathophysiology : the official journal of the International Society for Pathophysiology · 2026
    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

8 authors.

Daria S FominaState Budgetary Healthcare Institution of Moscow City "Moscow Clinical Research Center 7 Hospital No. 52 of the Moscow City Health Department", Moscow, Russia.
Olga A MukhinaState Budgetary Healthcare Institution of Moscow City "Moscow Clinical Research Center 7 Hospital No. 52 of the Moscow City Health Department", Moscow, Russia.
Elizaveta L SedovaState Budgetary Healthcare Institution of Moscow City "Moscow Clinical Research Center 7 Hospital No. 52 of the Moscow City Health Department", Moscow, Russia.
Marina S LebedkinaState Budgetary Healthcare Institution of Moscow City "Moscow Clinical Research Center 7 Hospital No. 52 of the Moscow City Health Department", Moscow, Russia.
Elena N BobrikovaFederal State Autonomous Educational Institution of Higher Education I.M.Sechenov First 12 Moscow State Medical University of the Ministry of Health of the Russian Federation 13, Sechenovskiy University, Moscow, Russia.
Alexander V KaraulovFederal State Autonomous Educational Institution of Higher Education I.M.Sechenov First 12 Moscow State Medical University of the Ministry of Health of the Russian Federation 13, Sechenovskiy University, Moscow, Russia.
Mariana A LysenkoState Budgetary Healthcare Institution of Moscow City "Moscow Clinical Research Center 7 Hospital No. 52 of the Moscow City Health Department", Moscow, Russia.
Harald RenzResearch Institute of Healthcare Organization and Medical Management of Moscow Department 10 of Healthcare, Moscow, Russia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Dupilumab is a fully human monoclonal antibody directed against the interleukin-4 receptor subunit α, the common chain of the IL-4 and IL-13 receptors. Dupilumab has been demonstrated to be highly effective in the treatment of severe atopic dermatitis, asthma, and chronic rhinosinusitis with nasal polyps. Despite the favorable tolerability of dupilumab, several publications and reviews have reported various adverse events, including conjunctivitis, keratitis, and face and neck treatment-resistant dermatitis, which reduce patients' quality of life and may necessitate the cancellation of therapy. The current standard of care for severe chronic diseases involves a collaborative approach between the patient and their physician. The majority of patients who respond well to this type of systemic atopic dermatitis (AtD) therapy are reluctant to interrupt dupilumab treatment due to the previously mentioned adverse events. The combination of dupilumab and anti-IgE therapy (omalizumab) may be beneficial for individuals who undergo dupilumab treatment for AtD and experience severe adverse events.

Indexed as

anti-IgE therapyatopic dermatitis (AtD)conjunctivitisdupilumabdupilumab-associated adverse effectsface and neck dermatitisomalizumab

Identifiers

PMID41626198
PMCPMC12855484

What OpenQuestion holds

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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.