Efficacy and safety of tofacitinib therapy in Asian patients with severe alopecia areata

Background: Patients with severe alopecia areata (AA), including alopecia totalis (AT) and alopecia universalis (AU), are usually resistant to treatment. While tofacitinib is emerging as a promising therapy for severe AA, little is known about its efficacy and safety in Asians. Objectives: To evalua...

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Main Authors: Ying-Xiu Dai, Chen-Pu Yeh, Chih-Chiang Chen
Format: Article
Language:English
Published: Wolters Kluwer Medknow Publications 2020-01-01
Series:Dermatologica Sinica
Subjects:
Online Access:http://www.dermsinica.org/article.asp?issn=1027-8117;year=2020;volume=38;issue=1;spage=3;epage=8;aulast=Dai
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spelling doaj-fb771b1eb48c4f00a0eef1df41700dd52020-11-25T02:50:34ZengWolters Kluwer Medknow PublicationsDermatologica Sinica1027-81172223-330X2020-01-013813810.4103/ds.ds_26_19Efficacy and safety of tofacitinib therapy in Asian patients with severe alopecia areataYing-Xiu DaiChen-Pu YehChih-Chiang ChenBackground: Patients with severe alopecia areata (AA), including alopecia totalis (AT) and alopecia universalis (AU), are usually resistant to treatment. While tofacitinib is emerging as a promising therapy for severe AA, little is known about its efficacy and safety in Asians. Objectives: To evaluate the efficacy and safety of tofacitinib for treating severe AA. Methods: We included patients with ≥50% scalp hair loss, disease for ≥6 months, and tofacitinib therapy for ≥4 months. The efficacy, evaluated based on the percent change in severity of alopecia tool (SALT) score, and response time, defined as time from baseline to reach >50% improvement in SALT score, were assessed. Results: We included 35 patients (21 with AA, 3 with AT, and 11 with AU). There were 18 men and 17 women (median age: 39 [range: 12–68] years). After 4–24 months of treatment, 74.3% showed clinical response, with 51.4% of the patients achieving ≥50% hair regrowth. Patients with AA showed higher percent change in SALT score than patients with AT/AU (median [interquartile range]: 60.7% [0–98.2] vs. 41.1% [8.9–98.7], P = 0.047). Initial SALT score was negatively associated with the latest percent change in SALT score (P = 0.025). Duration of disease and current episode were positively associated with response time to tofacitinib (P = 0.018 and 0.026, respectively). Patients tolerated tofacitinib well without serious adverse events. Conclusion: Tofacitinib effectively promoted hair regrowth in Asian patients with severe AA. Randomized controlled trials with larger sample size are needed to confirm the long-term efficacy and safety of tofacitinib for treating severe AA.http://www.dermsinica.org/article.asp?issn=1027-8117;year=2020;volume=38;issue=1;spage=3;epage=8;aulast=Daialopecia areatajanus kinase inhibitortofacitinibtreatment
collection DOAJ
language English
format Article
sources DOAJ
author Ying-Xiu Dai
Chen-Pu Yeh
Chih-Chiang Chen
spellingShingle Ying-Xiu Dai
Chen-Pu Yeh
Chih-Chiang Chen
Efficacy and safety of tofacitinib therapy in Asian patients with severe alopecia areata
Dermatologica Sinica
alopecia areata
janus kinase inhibitor
tofacitinib
treatment
author_facet Ying-Xiu Dai
Chen-Pu Yeh
Chih-Chiang Chen
author_sort Ying-Xiu Dai
title Efficacy and safety of tofacitinib therapy in Asian patients with severe alopecia areata
title_short Efficacy and safety of tofacitinib therapy in Asian patients with severe alopecia areata
title_full Efficacy and safety of tofacitinib therapy in Asian patients with severe alopecia areata
title_fullStr Efficacy and safety of tofacitinib therapy in Asian patients with severe alopecia areata
title_full_unstemmed Efficacy and safety of tofacitinib therapy in Asian patients with severe alopecia areata
title_sort efficacy and safety of tofacitinib therapy in asian patients with severe alopecia areata
publisher Wolters Kluwer Medknow Publications
series Dermatologica Sinica
issn 1027-8117
2223-330X
publishDate 2020-01-01
description Background: Patients with severe alopecia areata (AA), including alopecia totalis (AT) and alopecia universalis (AU), are usually resistant to treatment. While tofacitinib is emerging as a promising therapy for severe AA, little is known about its efficacy and safety in Asians. Objectives: To evaluate the efficacy and safety of tofacitinib for treating severe AA. Methods: We included patients with ≥50% scalp hair loss, disease for ≥6 months, and tofacitinib therapy for ≥4 months. The efficacy, evaluated based on the percent change in severity of alopecia tool (SALT) score, and response time, defined as time from baseline to reach >50% improvement in SALT score, were assessed. Results: We included 35 patients (21 with AA, 3 with AT, and 11 with AU). There were 18 men and 17 women (median age: 39 [range: 12–68] years). After 4–24 months of treatment, 74.3% showed clinical response, with 51.4% of the patients achieving ≥50% hair regrowth. Patients with AA showed higher percent change in SALT score than patients with AT/AU (median [interquartile range]: 60.7% [0–98.2] vs. 41.1% [8.9–98.7], P = 0.047). Initial SALT score was negatively associated with the latest percent change in SALT score (P = 0.025). Duration of disease and current episode were positively associated with response time to tofacitinib (P = 0.018 and 0.026, respectively). Patients tolerated tofacitinib well without serious adverse events. Conclusion: Tofacitinib effectively promoted hair regrowth in Asian patients with severe AA. Randomized controlled trials with larger sample size are needed to confirm the long-term efficacy and safety of tofacitinib for treating severe AA.
topic alopecia areata
janus kinase inhibitor
tofacitinib
treatment
url http://www.dermsinica.org/article.asp?issn=1027-8117;year=2020;volume=38;issue=1;spage=3;epage=8;aulast=Dai
work_keys_str_mv AT yingxiudai efficacyandsafetyoftofacitinibtherapyinasianpatientswithseverealopeciaareata
AT chenpuyeh efficacyandsafetyoftofacitinibtherapyinasianpatientswithseverealopeciaareata
AT chihchiangchen efficacyandsafetyoftofacitinibtherapyinasianpatientswithseverealopeciaareata
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