Evidence map›Paper›PMID 42340817›Full record

ArticleIndian dermatology online journal2026

A Pilot Randomized Controlled Trial Comparing the Efficacy and Safety of Oral Tofacitinib Versus Methotrexate In Moderate-to-Severe Alopecia Areata.

Mude Hemalatha, Tarun Narang, Muthu Sendhil Kumaran, Vinod Kumar, Hitaishi Mehta, Nusrat Shafiq, Daljit Kaur, Sunil Dogra

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Article in Indian dermatology online journal, 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

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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

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

8 authors.

Mude HemalathaDepartment of Dermatology, Venereology and Leprology, Postgraduate Institute of Medical Education and Research, Chandigarh, India.ORCID 0009-0001-1156-3613
Tarun NarangDepartment of Dermatology, Venereology and Leprology, Postgraduate Institute of Medical Education and Research, Chandigarh, India.
Muthu Sendhil KumaranDepartment of Dermatology, Venereology and Leprology, Postgraduate Institute of Medical Education and Research, Chandigarh, India.
Vinod KumarDepartment of Dermatology, Venereology and Leprology, Postgraduate Institute of Medical Education and Research, Chandigarh, India.
Hitaishi MehtaDepartment of Dermatology, Venereology and Leprology, Postgraduate Institute of Medical Education and Research, Chandigarh, India.
Nusrat ShafiqDepartment of Pharmacology, Postgraduate Institute of Medical Education and Research, Chandigarh, India.
Daljit KaurDepartment of Dermatology, Venereology and Leprology, Postgraduate Institute of Medical Education and Research, Chandigarh, India.
Sunil DograDepartment of Dermatology, Venereology and Leprology, Postgraduate Institute of Medical Education and Research, Chandigarh, India.ORCID 0000-0001-9912-0085

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundTreatments for moderate-to-severe alopecia areata (AA) have limited efficacy. Methotrexate, a conventional immunosuppressant, has been used for AA, while Janus kinase/signal transducer and activator of transcription (JAK-STAT) inhibitors like tofacitinib have shown promising results.

objectiveTo compare the efficacy of tofacitinib and methotrexate in moderate-to-severe AA. PATIENTS AND

methodsThirty-six patients aged 18-60 years with a severity of alopecia tool (SALT) score >40 were randomized to receive either tofacitinib (5-10 mg twice daily) or methotrexate (0.3-0.5 mg/kg weekly) for 6 months, followed by 3-month follow-up. Primary outcomes measured the proportion achieving a SALT score ≤20 at 6 months. Secondary outcomes included patient-reported outcome (PRO) on scalp hair assessment, dermatology life quality index (DLQI), patient health questionnaire (PHQ) scores, relapse rates, and alkaline phosphatase (ALP) activity in scalp biopsies.

resultsAt 6 months, 50% of tofacitinib patients achieved a SALT score ≤20 vs. 33.3% with methotrexate ( P = 0.31). A ≥ 90% SALT improvement occurred in 33.3% of tofacitinib and 11.1% of methotrexate patients ( P = 0.10). The tofacitinib group had greater scalp hair PRO score reductions. Both groups showed significant DLQI and PHQ improvements, with no intergroup differences. Adverse events were reported in 38.8% of tofacitinib and 33.3% of methotrexate patients ( P = 1). ALP activity was inconclusive. LIMITATIONS: Small sample size, open-label design, lack of stratification, and baseline imbalances that may affect achievable improvement and comparative interpretation.

conclusionIn this pilot trial, both tofacitinib and methotrexate improved SALT score, PRO score, and psychological outcomes, but the tofacitinib group showed greater efficacy. Larger studies are warranted to confirm findings and investigate ALP activity.

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PMID42340817
PMCPMC13395296

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