Evidence map›Paper›PMID 40192965›Full record

Observational studyAdvances in therapy2025

Baseline Characteristics and Treatment Patterns of Patients with Atopic Dermatitis Treated with Oral Systemic Therapies: An Interim Analysis of the AD-REAL Study.

Matthias Augustin, Esther Serra-Baldrich, Julien Seneschal, Susanne Grond, Anastasia Lampropoulou, Mohamed Elrayes, Samuel Ogwu, Inmaculada de la Torre, Anthony Bewley, Andreas Pinter

Abstract readObservational StudyMulticenter Study
In one paragraph

Observational study in Advances in therapy, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed, 1 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

2 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
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.

Matthias AugustinInstitute for Health Services Research in Dermatology and Nursing (IVDP), University Medical Center Hamburg-Eppendorf (UKE), Hamburg, Germany. m.augustin@uke.de.
Esther Serra-BaldrichDepartment of Dermatology, Cutaneous Allergy Unit, Hospital de la Santa Crue i Sant Pau, Universitat Autònoma de Barcelona, Barcelona, Spain.
Julien SeneschalDepartment of Dermatology, National Reference Center for Rare Skin Diseases, University of Bordeaux, Bordeaux, France.
Susanne GrondEli Lilly and Company Ltd., Indianapolis, IN, USA.
Anastasia LampropoulouEli Lilly and Company Ltd., Indianapolis, IN, USA.
Mohamed ElrayesEli Lilly and Company Ltd., Indianapolis, IN, USA.
Samuel OgwuEli Lilly and Company Ltd., Indianapolis, IN, USA.
Inmaculada de la TorreEli Lilly and Company Ltd., Indianapolis, IN, USA.
Anthony BewleyDepartment of Dermatology, Barts Health NHS Trust & Queen Mary University of London, London, UK.
Andreas PinterDepartment of Dermatology, Venereology and Allergology, University Hospital Frankfurt, Frankfurt am Main, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionAD-REAL is an ongoing 1-year multinational observational cohort study evaluating oral systemic therapies in the management of adults with atopic dermatitis (AD) in a real-world practice across four European countries. Herein, we provide insights on baseline disease characteristics and treatment patterns of patients treated with oral systemic therapies, including baricitinib.

methodsAD-REAL included adults with moderate-to-severe AD for ≥ 6 months, who were initiated on an oral systemic treatment in clinical practice and enrolled either in the baricitinib or the other oral systemic (OOS) cohort. Here, we report baseline characteristics, including clinician-assessed outcomes (Eczema Area and Severity Index [EASI]) and patient-reported outcomes (PROs), and explore AD subgroups based on body surface area (BSA) ≤ 40% and Itch numerical rating scale (NRS) ≥ 7. Continuous outcomes were reported using mean and standard deviation (SD) and categorical variables using frequencies. Baseline continuous variables with missing data were imputed using the multiple imputation method.

resultsBaseline demographics were consistent across both baricitinib and OOS cohorts. Patients showed long disease duration (26.2 years), refractory to several systemic options, and a moderate EASI mean (SD) score of 17.5 (10.7). The majority (53.7%) presented with severe Validated Investigator Global Assessment (vIGA) and highly impacted Dermatology Life Quality Index (DLQI) score (14.0 [7.1]). At baseline, patients were predominantly female, with AD mainly affecting face/neck (89.4%) and upper extremities (90.3%). About 68.4% presented with BSA ≤ 40 and 33.8% with BSA ≤ 40 and Itch NRS ≥ 7. From those with BSA ≤ 40% and Itch NRS ≥ 7, 63.9% were treated with Janus kinase inhibitors (JAKi).

conclusionThis analysis provides key information on baseline disease characteristics of patients treated with oral systemics, including baricitinib. Most patients treated with oral systemics in AD-REAL had long-lasting disease, refractory to systemic therapies, with moderate skin affectation but severe itch and impact on quality of life. AD-REAL is the first study to show many patients in real-world practice who are treated with oral systemics present with BSA ≤ 40 and Itch NRS ≥ 7, and most of these patients were treated with JAKi.

Indexed as

AzetidinesDermatitis, AtopicSulfonamidesAdministration, OralAdultFemaleHumansMaleMiddle AgedPatient Reported Outcome MeasuresPurinesPyrazolesQuality of LifeSeverity of Illness IndexAzetidinesbaricitinibPurinesPyrazolesSulfonamidesAtopic dermatitisOral systemic treatmentsSevere itch

Identifiers

PMID40192965
PMCPMC12085387

What OpenQuestion holds

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LicenceCC BY-NC
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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.