Evidence map›Paper›PMID 42348162›Full record

ArticlePaediatric drugs2026

Real-World Systemic Treatment Patterns and Outcomes of Children With Severe Alopecia Areata: A French Nationwide Study (ESTAPED Cohort).

Ninon Le Goaziou, Christine Bodemer, Christine Labrèze, Emmanuel Mahé, Annabel Maruani, Helene Aubert, Sébastien Barbarot, Claire Abasq, Nina Sigg, Audrey Lasek and 9 more

Abstract readMulticenter Study
In one paragraph

Article in Paediatric drugs, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

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4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

19 authors.

Ninon Le GoaziouDepartment of Dermatology, CHU Rennes, 35000, Rennes, France.
Christine BodemerDepartment of Dermatology, Hôpital Necker Enfants Malades - Assistance Publique-Hôpitaux de Paris, Paris, France.
Christine LabrèzeDepartment of Dermatology, CHU Bordeaux, Bordeaux, France.
Emmanuel MahéDepartment of Dermatology, CH Argenteuil, Argenteuil, France.
Annabel MaruaniDepartment of Dermatology, CHU Tours, Tours, France.
Helene AubertDepartment of Dermatology, CHU Nantes, Nantes, France.
Sébastien BarbarotDepartment of Dermatology, CHU Nantes, Nantes, France.
Claire AbasqDepartment of Dermatology, CHU Brest, Brest, France.
Nina SiggDepartment of Dermatology, CHU Angers, Angers, France.
Audrey LasekDepartment of Dermatology, Hôpital Saint Vincent de Paul, Université Catholique de Lille, Lille, France.
Stéphanie MalletDepartment of Dermatology, CHU Marseille, Marseille, France.
Christine ChiaveriniDepartment of Dermatology, CHU Nice, Nice, France.
Juliette MiquelDepartment of Dermatology, CHU La Réunion, La Réunion, France.
Eve PuzenatDepartment of Dermatology, CHU Besançon, Besançon, France.
Florence PoizeauDepartment of Dermatology, CHU Rennes, 35000, Rennes, France.
Jasmine FlamentDepartment of Dermatology, CHU Rouen, Rouen, France.
Bertille BonniaudDepartment of Dermatology, CHU Dijon, Dijon, France.
Justine PasteurDepartment of Dermatology, CHU Clermont-Ferrand, Clermont-Ferrand, France.
Catherine DroitcourtDepartment of Dermatology, CHU Rennes, 35000, Rennes, France. catherine.droitcourt@chu-rennes.fr.ORCID http://orcid.org/0000-0001-6714-6643

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND/

objectiveSevere forms of alopecia areata (AA) often require off-label systemic treatments (ST) for which data on effectiveness and safety are limited. This study aimed to provide a comprehensive real-world overview of ST patterns in children with severe AA.

methodWe conducted a retrospective, longitudinal, multicenter study of children with AA (aged <18 years) receiving at least one ST (2010-2023), identified using a keyword search in Ouest Data Hub Warehouse (a hospital data network in France with a critical mass of 5.1 million patients) or by members of the Société Française de Dermatologie Pédiatrique. The primary outcome was drug survival (DS), defined as time on ST, and the secondary outcomes included reasons for treatment discontinuation and long-term observations.

resultsAmong the 262 included children (median age at AA onset: 9 years; 58.4% girls, atopic dermatitis in 32.4%), the first-line ST most frequently initiated (median age: 12 years, alopecia totalis in 28.6%) was intravenous corticosteroids (35.9%, median duration: 3 months), followed by methotrexate + intravenous corticosteroids (24.0%, 12.5 months), oral corticosteroids (17.9%, 1 month), methotrexate (10.7%, 9.5 months), methotrexate + oral corticosteroids (8.8%, 9 months), and lastly baricitinib (2.7%, 2.5 months). Specific maintenance treatments were not significantly associated with DS. Psychological impact, atopic dermatitis, later childhood onset and female sex were associated with longer first-line systemic treatment drug survival. Treatment failure was the main reason for discontinuation (51.9%) and no serious adverse events were reported. Five years after starting the first ST (n = 62), 14.5% of patients had achieved remission.

conclusionsIn this national, retrospective real-world study, drug survival analyses highlighted two treatment profiles: pulse therapy (corticosteroids) for flare-ups and maintenance treatments (methotrexate, baricitinib) for long-term management. Overall, the effectiveness of therapies appears limited with frequent relapse and a likely need for prolonged treatment. However, data on long-term treatment outcomes of JAKi in children are lacking. This study provides real-life data which could help improve management strategies in children with severe AA.

Indexed as

Adrenal Cortex HormonesAlopecia AreataAdolescentChildChild, PreschoolFemaleFranceHumansLongitudinal StudiesMaleMethotrexateOff-Label UseRetrospective StudiesSeverity of Illness IndexSulfonamidesTreatment OutcomeAdrenal Cortex HormonesMethotrexateSulfonamides

Identifiers

PMID42348162
PMCPMC13379489

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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.