Evidence map›Paper›PMID 39998595›Full record

ArticleArchives of dermatological research2025

Switching JAK inhibitors: evaluating baricitinib's effectiveness in alopecia areata after tofacitinib failure.

Ala Ehsani, Zahra Razavi, Amirhossein Rahimnia, Amirhoushang Ehsani, Fatemeh Saberi, Zeinab Aryanian, Hanie Babaie

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Article in Archives of dermatological research, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

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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

7 authors.

Ala EhsaniSchool of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
Zahra RazaviAutoimmune Bullous Diseases Research Center, Razi Hospital, Tehran University of Medical Sciences, Tehran, Iran.
Amirhossein RahimniaAutoimmune Bullous Diseases Research Center, Razi Hospital, Tehran University of Medical Sciences, Tehran, Iran.
Amirhoushang EhsaniAutoimmune Bullous Diseases Research Center, Razi Hospital, Tehran University of Medical Sciences, Tehran, Iran.
Fatemeh SaberiAutoimmune Bullous Diseases Research Center, Razi Hospital, Tehran University of Medical Sciences, Tehran, Iran.
Zeinab AryanianAutoimmune Bullous Diseases Research Center, Razi Hospital, Tehran University of Medical Sciences, Tehran, Iran.
Hanie BabaieAutoimmune Bullous Diseases Research Center, Razi Hospital, Tehran University of Medical Sciences, Tehran, Iran. haniebabaie17@gmail.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Alopecia areata (AA) is a condition of hair loss with an immune-mediated cause. The efficacy of switching to a different JAK inhibitor in a patient who has failed to respond to one JAK inhibitor for AA is also unknown. This review is to examine the efficacy and safety of baricitinib in patients' inadequate response to tofacitinib. This is a retrospective study of 26 patients with AA who were switched from tofacitinib to baricitinib because of insufficient response, side effects or disease relapse. The patients had a mean age of 31 years, with 65% being female. The SALT score was reduced from 90 ± 19 to 68 ± 31 (p < 0.05) in an average of 16 months of tofacitinib treatment. However, the SALT score was reduced from 68 ± 31 to 50 ± 31 (p < 0.05) in about 7 months of baricitinib treatment. 34.6% of patients taking tofacitinib and 19.2% of patients receiving baricitinib did not respond to the treatment; however, 66.66% of the tofacitinib non-responders had improvement with baricitinib. Of the five patients with unchanged SALT scores after tofacitinib, four (80%) had an average reduction of 58.25 points with baricitinib. Baricitinib induced eyebrow and eyelash regrowth in 60% of AU (Alopecia Universalis) patients. Both treatments brought down SALT scores in pediatric cases. Adverse effects were mild and were noted in 30.76% of patients on tofacitinib and 3.84% of patients on baricitinib treatment. Oral baricitinib is safe with minimal side effects and also effective for both pediatric and adult AA patients who are inadequate responders to tofacitinib. These findings need to be confirmed by further research.

Indexed as

Alopecia AreataAzetidinesJanus Kinase InhibitorsPiperidinesPyrazolesPyrimidinesPyrrolesSulfonamidesAdolescentAdultDrug SubstitutionFemaleHumansMaleMiddle AgedPurinesAzetidinesbaricitinibJanus Kinase InhibitorsPiperidinesPurinesPyrazolesPyrimidinesPyrrolesSulfonamidestofacitinibAlopecia areataBaricitinibJAK inhibitorsTofacitinibTreatment

Identifiers

PMID39998595

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.