Evidence map›Paper›PMID 42217072›Full record

ArticleDermatology and therapy2026

Real-World Ritlecitinib Treatment of Severe Alopecia Areata in the United States: Patient Characteristics and Physician Satisfaction According to a Secondary Database Analysis.

Samantha K Kurosky, Ashley S Cha-Silva, Jenny Austin, Arash Mostaghimi, Chesahna Kindred, Genevieve Gauthier, Mojgan Sadrarhami, Peter Anderson, Benjamin Ungar

Abstract read
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Article in Dermatology and therapy, 2026. 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
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2citing papers in PubMed
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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

9 authors.

Samantha K KuroskyPfizer Inc, New York, NY, USA. Samantha.Kurosky@pfizer.com.
Ashley S Cha-SilvaPfizer Inc, New York, NY, USA.
Jenny AustinAdelphi Real World, Bollington, UK.
Arash MostaghimiBrigham and Women's Hospital, Boston, MA, USA.
Chesahna KindredKindred Hair & Skin Center, Columbia, MD, USA.
Genevieve GauthierPfizer Inc, Kirkland, QC, Canada.
Mojgan SadrarhamiPfizer Inc, New York, NY, USA.
Peter AndersonAdelphi Real World, Bollington, UK.
Benjamin UngarMount Sinai, New York, NY, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionRitlecitinib, an oral, selective dual inhibitor of Janus kinase (JAK) 3 and tyrosine kinase expressed in hepatocellular carcinoma (TEC) family kinases, is approved for treating severe alopecia areata (AA) in patients aged ≥ 12 years in the USA. This study describes characteristics, treatment satisfaction, and success among adults initiating ritlecitinib.

methodsA sample of US dermatologists treating adults who received ritlecitinib for severe AA were surveyed between November 2023 and June 2024. Demographics, clinical characteristics, treatment history, satisfaction, and health-related quality of life were analyzed overall, among recent initiators, and stratified by treatment duration.

resultsA total of 123 adults were included (mean age 37.1 years; 57% male; 79% white; 88% commercial insurance). Mean disease duration was 2.1 years. At ritlecitinib initiation (n = 93), mean scalp hair loss was 71% and 73% had worsening AA. The proportion of patients with hair regrowth increased with longer treatment duration, 49% among those with < 3 months of treatment (n = 18/37) to 82% with > 6 months (n = 28/34). Physicians reported many recent initiators (n = 26) felt moderate/severe embarrassment (84%), frustration (73%), and anxiety (65%) due to their AA. Among patients with available data (n = 102), ritlecitinib was the first AA treatment for 46%. Treatment goals (n = 123) included reducing hair loss (94%), improving quality-of-life (41%), and achieving long-term control (32%). Reasons for selecting ritlecitinib (n = 113) included its ability to reduce scalp hair loss (38%), cost-benefit ratio (28%), and safety profile (25%). Satisfaction with AA control was 54%, 68%, and 85% after < 3 (n = 20/37), 3-6 (n = 27/40), and > 6 months (n = 29/34), respectively, of ritlecitinib treatment.

conclusionsMany patients experienced psychological burden due to their AA around the start of treatment. Ritlecitinib was chosen for its efficacy, safety, and cost-effectiveness. Hair regrowth, disease stability, and treatment satisfaction increased with longer ritlecitinib treatment duration suggesting sustained treatment is important for achieving treatment goals.

Indexed as

Alopecia areataReal-world dataRitlecitinib

Identifiers

PMID42217072
PMCPMC13280082

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