Evidence map›Paper›PMID 41247178›Full record

Observational studyActa dermato-venereologica2025

Successful Dose Reduction of Janus-kinase Inhibitors in Well-controlled Atopic Dermatitis: A Prospective, Multicentre, Real-world Study.

Anne R Schlösser, Anouk G M Caron, Merle S Den Ouden, Sara J Baart, Louise A A Gerbens, Phyllis I Spuls, Tamar E C Nijsten, Renske Schappin, DirkJan Hijnen

Abstract readMulticenter StudyObservational Study
In one paragraph

Observational study in Acta dermato-venereologica, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  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

9 authors.

Anne R SchlösserDepartment of Dermatology, Erasmus University Medical Center, Rotterdam, The Netherlands.
Anouk G M Caron *Department of Dermatology, Amsterdam University Medical Center, Amsterdam, The Netherlands.ORCID 0000-0002-5793-2664
Merle S Den Ouden *Department of Dermatology, Erasmus University Medical Center, Rotterdam, The Netherlands.
Sara J BaartDepartment of Biostatistics, Erasmus University Medical Center, Rotterdam, the Netherlands.ORCID 0000-0002-1427-901X
Louise A A GerbensDepartment of Dermatology, Amsterdam University Medical Center, Amsterdam, The Netherlands.ORCID 0000-0002-5244-5058
Phyllis I SpulsDepartment of Dermatology, Amsterdam University Medical Center, Amsterdam, The Netherlands.ORCID 0000-0002-6035-2863
Tamar E C NijstenDepartment of Dermatology, Erasmus University Medical Center, Rotterdam, The Netherlands.ORCID 0000-0001-9940-2875
Renske SchappinDepartment of Dermatology, Erasmus University Medical Center, Rotterdam, The Netherlands.ORCID 0000-0002-5727-5852
DirkJan HijnenDepartment of Dermatology, Erasmus University Medical Center, Rotterdam, The Netherlands. dirkjan.hijnen@radboudumc.nl.ORCID 0000-0003-3379-3425

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Janus kinase 1 (JAK1) inhibitors are effective for atopic dermatitis, but carry risks of adverse events. Dose reduction may mitigate these risks, although real-world evidence of dose reduction strategies is limited. This prospective, real-world study investigated JAK1 inhibitor dose reduction among 60 adults with controlled atopic dermatitis treated with abrocitinib or upadacitinib for ≥ 3 months. Doses were halved or administered every other day, as capsules cannot be split. Patients could resume their original dose if needed. The primary outcome was the proportion of patients maintaining the reduced dose at week 12. Secondary outcomes included physician- and patient-reported measures at baseline, and weeks 4, 8, and 12, analysed using linear mixed-effects models. At week 12, 80% (48/60) maintained the reduced dose. All outcomes remained within treat-to-target goals for atopic dermatitis at week 12, except for POEM (mean 8.87, 95% CI 7.43-10.31). While disease activity was significantly increased at week 8, no changes were seen at week 12. Absolute changes did not exceed the minimal clinically important difference. All 8 patients who resumed their initial dose regained disease control at week 12. In conclusion, JAK1 inhibitor dose reduction was feasible in 80% of patients without a clinically meaningful increase in disease activity.

Indexed as

Dermatitis, AtopicDrug TaperingHeterocyclic Compounds, 3-RingJanus Kinase 1Janus Kinase InhibitorsPyrimidinesSulfonamidesAdultFemaleHumansMaleMiddle AgedProspective StudiesTime FactorsTreatment OutcomeYoung AdultabrocitinibHeterocyclic Compounds, 3-RingJAK1 protein, humanJanus Kinase 1Janus Kinase InhibitorsPyrimidinesSulfonamidesupadacitinib

Identifiers

PMID41247178
PMCPMC12632132

What Socratic holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

Registered trials

None linked

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 Socratic graph.