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Real-world effectiveness and safety of tofacitinib for alopecia areata: A retrospective cohort study of 202 patients.
Cranwell, William; Meah, Nekma; Wall, Dmitri; Bhoyrul, Bevin; Laita, Bokhari; Sinclair, Rodney D.
Affiliation
  • Cranwell W; Sinclair Dermatology, Melbourne, Victoria, Australia.
  • Meah N; St Helens & Knowsley NHS Trust, Prescot, UK.
  • Wall D; Faculty of Biology, Medicine and Health, Manchester University, Manchester, UK.
  • Bhoyrul B; National and International Skin Registry Solutions (NISR), Dublin, Ireland.
  • Laita B; Hair Restoration Blackrock, Dublin, Ireland.
  • Sinclair RD; Charles Institute of Dermatology, School of Medicine, University College Dublin, Dublin, Ireland.
Article de En | MEDLINE | ID: mdl-38831704
ABSTRACT

BACKGROUND:

Alopecia areata (AA) is an autoimmune hair loss disorder characterised by collapse of hair follicle immune privilege and mediated by autoreactive CD8+ T lymphocytes and natural killer cells. Treatment is often unsatisfactory. The Janus kinase-signal transducer and activator of transcription (JAK-STAT) pathway is implicated in the pathogenesis of AA and Janus Kinase inhibitor (JAKi) medications are promising emerging treatments for AA.

OBJECTIVES:

We evaluated the safety and effectiveness of tofacitinib in a real-world setting over 18 months of treatment.

METHODS:

A retrospective cohort study of all patients with scalp AA commenced on tofacitinib between 1 November 2016 and 31 May 2019. The primary endpoint was the percent change in Severity of Alopecia Tool (SALT) score at 18 months.

RESULTS:

Two hundred and two patients were included. After 18 months of treatment, 55.9%, 42.6% and 29.2% achieved 50%, 75% and 90% reductions in their SALT scores respectively. Increased duration of AA was a negative predictor of hair regrowth. Males and patients with baseline SALT ≥90 were slower to respond to treatment in the first 12 months. One hundred and twenty-four patients and 168 patients received concomitant systemic corticosteroids or low-dose oral minoxidil during tofacitinib therapy respectively. There were no serious adverse events.

CONCLUSION:

Tofacitinib was a safe and effective treatment for patients with moderate-to-severe AA. Further randomised controlled studies are needed to establish the optimal treatment regimen.
Mots clés

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Langue: En Journal: Australas J Dermatol Année: 2024 Type de document: Article Pays d'affiliation: Australie

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Langue: En Journal: Australas J Dermatol Année: 2024 Type de document: Article Pays d'affiliation: Australie