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Tofacitinib in Pediatric Alopecia Areata Totalis and Alopecia Universalis: A Retrospective Analysis From India.
Gowda, Shreya K; Aggarwal, Akash; Thakur, Vishal; Behera, Biswanath; Garg, Sonika; Sethy, Madhusmita; Ayyanar, Pavithra.
Afiliación
  • Gowda SK; Department of Dermatology and Venereology, All India Institute of Medical Sciences, Bhubaneswar, India.
  • Aggarwal A; Department of Dermatology and Venereology, All India Institute of Medical Sciences, Bhubaneswar, India.
  • Thakur V; Department of Dermatology and Venereology, All India Institute of Medical Sciences, Bhubaneswar, India.
  • Behera B; Department of Dermatology and Venereology, All India Institute of Medical Sciences, Bhubaneswar, India.
  • Garg S; Department of Dermatology and Venereology, All India Institute of Medical Sciences, Bhubaneswar, India.
  • Sethy M; Department of Pathology and Lab Medicine, All India Institute of Medical Sciences, Bhubaneswar, India.
  • Ayyanar P; Department of Pathology and Lab Medicine, All India Institute of Medical Sciences, Bhubaneswar, India.
J Cutan Med Surg ; : 12034754241266128, 2024 Jul 26.
Article en En | MEDLINE | ID: mdl-39056399
ABSTRACT
Alopecia areata totalis and universalis are disabling conditions and therapeutically challenging as they are refractory to conventional options. Tofacitinib is a Janus-kinase (JAK) inhibitor utilized to treat alopecia areata (AA) as an off-label drug. In India, FDA-approved JAK inhibitors such as baricitinib and ritlecitinib are not available. There are only a few case reports on tofacitinib in AA in the Indian population. We present the data of 9 pediatric cases of clinically and histologically proven alopecia areata totalis (AT) and alopecia universalis (AU), for whom oral tofacitinib was given after baseline investigations. The following parameters were analysed Photographic image and severity of alopecia tool (SALT) score at baseline, 3 months and 6 months, and Children Dermatology Life Quality Index (cDLQI) at baseline and 6 months. The mean ± standard deviation (M ± SD) of the SALT score and cDLQI(M ± SD) at baseline were 95 ± 5 and 17 ± 2. At weeks 4 and weeks 12, the SALT (M ± SD) score was 92.7 ± 6.1 and 34.35 ± 11.16, respectively. At weeks 24, the SALT (M ± SD) score and cDLQI (M ± SD) were 3.33 ± 5 and 6 ± 2. The final reduction in SALT score from the baseline was 100% in 6/9 cases (66.67%), 75% to 99% in 3/9 (22.23%), and 50 to 75% in 1/9 (11.12%). We also observed minimal adverse effects (one child developed herpes zoster) with tofacitinib. Our study demonstrates that oral tofacitinib represents a viable modality in managing difficult-to-treat pediatric AA, such as AT and AU, with a good safety profile.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: J Cutan Med Surg Asunto de la revista: DERMATOLOGIA Año: 2024 Tipo del documento: Article País de afiliación: India Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: J Cutan Med Surg Asunto de la revista: DERMATOLOGIA Año: 2024 Tipo del documento: Article País de afiliación: India Pais de publicación: Estados Unidos