Evidence map›Paper›PMID 27699252›Full record

ArticleJCI insight2016

Safety and efficacy of the JAK inhibitor tofacitinib citrate in patients with alopecia areata.

Milène Kennedy Crispin, Justin M Ko, Brittany G Craiglow, Shufeng Li, Gautam Shankar, Jennifer R Urban, James C Chen, Jane E Cerise, Ali Jabbari, Mårten Cg Winge and 4 more

2 registry-linked trialsOpen access · goldAbstract readMulticenter Study
In one paragraph

Article in JCI insight, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Cited by 150 papers, 6 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
150citing papers in PubMed, 6 pooled it
43.1field-weighted citation impact, top 1% of its field
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.

NCT02197455 phase2completednot on this map

Tofacitnib for the Treatment of Alopecia Areata and Variants

TypeinterventionalSponsorYale UniversityRan2014 to 2015Enrolled30ConditionsAlopecia Areata (AA), Alopecia Totalis (AT), Alopecia Universalis (AU)ArmsTofacitinib Administration
NCT02312882 nacompletednot on this map

Tofacitinib for the Treatment of Alopecia Areata and Its Variants

TypeinterventionalSponsorStanford UniversityRan2014 to 2015Enrolled40ConditionsAlopecia Areata, Alopecia Totalis, Alopecia UniversalisArmsTofacitinib
3 · Its place in the literature

Who cites it

150 citing papers in PubMed, 6 syntheses or guidelines pooled it, 340 citations in OpenAlex.

  1. Pooled it
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  7. Trial
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  9. Review
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  11. Article
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  16. Pharmacologic Inhibition of JAK1/2 Potentiates Aminoglycoside-Induced Ototoxicity.Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology · 2026
    Article
  17. Review
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90 more citing papers are in PubMed but not listed here.

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

14 authors at 5 institutions in 1 country.

Milène Kennedy CrispinProgram in Epithelial Biology and Department of Dermatology, Stanford University School of Medicine, Stanford, California, USA.
Justin M KoProgram in Epithelial Biology and Department of Dermatology, Stanford University School of Medicine, Stanford, California, USA.
Brittany G CraiglowDepartment of Dermatology.
Shufeng LiProgram in Epithelial Biology and Department of Dermatology, Stanford University School of Medicine, Stanford, California, USA.
Gautam ShankarProgram in Epithelial Biology and Department of Dermatology, Stanford University School of Medicine, Stanford, California, USA.
Jennifer R UrbanDepartment of Internal Medicine, Yale University School of Medicine, New Haven, Connecticut, USA.
James C ChenDepartment of Dermatology.
Jane E CeriseDepartment of Dermatology.
Ali JabbariDepartment of Dermatology.
Mårten Cg WingeProgram in Epithelial Biology and Department of Dermatology, Stanford University School of Medicine, Stanford, California, USA.
M Peter MarinkovichProgram in Epithelial Biology and Department of Dermatology, Stanford University School of Medicine, Stanford, California, USA.
Angela M ChristianoDepartment of Dermatology.
Anthony E OroProgram in Epithelial Biology and Department of Dermatology, Stanford University School of Medicine, Stanford, California, USA.
Brett A KingDepartment of Dermatology.
Stanford University · USCenter for Systems Biology · USColumbia University · USPediatrics and Genetics · USYale University · US

Funding

Project 1: Translational Science of Alopecia AreataP50AR070588 · NIAMS · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI CHRISTIANO, ANGELA M · 2016 to 2021
$8.0M
PREDOCTORAL TRAINING GRANT IN HUMAN GENETICS &DEVELOPMET32GM007088 · NIGMS · COLUMBIA UNIV NEW YORK MORNINGSIDE · PI SHEN, MICHAEL M. · 1985 to 2020
$7.1M
Laminins in the SkinR01AR047223 · NIAMS · STANFORD UNIVERSITY · PI MARINKOVICH, MATT PETER · 2000 to 2013
$4.8M
REGULATING GLI FUNCTION IN HAIR FOLLICLE PROGENITORSR01AR054780 · NIAMS · STANFORD UNIVERSITY · PI ORO, ANTHONY E · 2007 to 2017
$4.3M
Developing an Alopecia Areata Disease Activity Index (ALADIN)U01AR067173 · NIAMS · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI CHRISTIANO, ANGELA M · 2014 to 2016
$734k
NIAMS NIH HHS P50 AR070588NIAMS NIH HHS R01 AR047223NIAMS NIH HHS R01 AR054780NIAMS NIH HHS U01 AR067173NIGMS NIH HHS T32 GM007088
6 · The paper itself

Abstract

backgroundAlopecia areata (AA) is an autoimmune disease characterized by hair loss mediated by CD8

methodsThis was a 2-center, open-label, single-arm trial using the pan-JAK inhibitor, tofacitinib citrate, for AA with >50% scalp hair loss, alopecia totalis (AT), and alopecia universalis (AU). Tofacitinib (5 mg) was given twice daily for 3 months. Endpoints included regrowth of scalp hair, as assessed by the severity of alopecia tool (SALT), duration of hair growth after completion of therapy, and disease transcriptome.

resultsOf 66 subjects treated, 32% experienced 50% or greater improvement in SALT score. AA and ophiasis subtypes were more responsive than AT and AU subtypes. Shorter duration of disease and histological peribulbar inflammation on pretreatment scalp biopsies were associated with improvement in SALT score. Drug cessation resulted in disease relapse in 8.5 weeks. Adverse events were limited to grade I and II infections. An AA responsiveness to JAK/STAT inhibitors score was developed to segregate responders and nonresponders, and the previously developed AA disease activity index score tracked response to treatment.

conclusionsAt the dose and duration studied, tofacitinib is a safe and effective treatment for severe AA, though it does not result in a durable response. Transcriptome changes reveal unexpected molecular complexity within the disease.

trial registrationClinicalTrials.gov NCT02197455 and NCT02312882.

fundingThis work was supported by the US Department of Veterans Affairs Office of Research and Development, National Institute of Arthritis and Musculoskeletal and Skin Diseases National Institutes of Health grant R01 AR47223 and U01 AR67173, the National Psoriasis Foundation, the Swedish Society of Medicine, the Fernström Foundation, the Locks of Love Foundation, the National Alopecia Areata Foundation, and the Ranjini and Ajay Poddar Resource Fund for Dermatologic Diseases Research.

Indexed as

AdultAgedAlopecia AreataFemaleHumansJanus Kinase InhibitorsMaleMiddle AgedPiperidinesPyrimidinesPyrrolesUnited StatesYoung AdultJanus Kinase InhibitorsPiperidinesPyrimidinesPyrrolestofacitinib

Identifiers

PMID27699252
PMCPMC5033755
OpenAlexW2521655245

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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.