Tofacitinib monotherapy as maintenance treatment in juvenile dermatomyositis: a case report

Juvenile dermatomyositis (JDM) is a multisystem autoimmune disease associated with considerable morbidity and mortality, having a significant impact on patient health. Early diagnosis and appropriate treatment play a key role in optimising outcomes. JDM management remains challenging, particularly in severe or refractory cases, due to the limited evidence regarding therapeutic options. Given these challenges, Janus kinase inhibitors, including tofacitinib, have emerged as promising alternatives, yet evidence in paediatric populations is still scarce. We present the case of a child with JDM who achieved sustained remission with tofacitinib monotherapy following the failure of previous therapies. While its use is currently restricted to refractory cases, these findings suggest its potential for earlier integration into treatment algorithms. This work aims to provide valuable insights to guide therapeutic strategies in JDM.

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Publication Details

Journal
RMD Open
Published
2025-04-01
DOI
https://doi.org/10.1136/rmdopen-2025-005651
Citations
2
Primary Topic
Inflammatory Myopathies and Dermatomyositis
Type
article
Field-Weighted Citation Impact
2.71
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article

Tofacitinib monotherapy as maintenance treatment in juvenile dermatomyositis: a case report

Montserrat M. Díaz Encarnación, E. Calvo, Estefanía Barral Mena, D. Balas
2 citations
RMD Open
Inflammatory Myopathies and Dermatomyositis
2.71
article

Tofacitinib monotherapy as maintenance treatment in juvenile dermatomyositis: a case report

Montserrat M. Díaz Encarnación, E. Calvo, Estefanía Barral Mena, D. Balas
article en
2 citations

Abstract

Juvenile dermatomyositis (JDM) is a multisystem autoimmune disease associated with considerable morbidity and mortality, having a significant impact on patient health. Early diagnosis and appropriate treatment play a key role in optimising outcomes. JDM management remains challenging, particularly in severe or refractory cases, due to the limited evidence regarding therapeutic options. Given these challenges, Janus kinase inhibitors, including tofacitinib, have emerged as promising alternatives, yet evidence in paediatric populations is still scarce. We present the case of a child with JDM who achieved sustained remission with tofacitinib monotherapy following the failure of previous therapies. While its use is currently restricted to refractory cases, these findings suggest its potential for earlier integration into treatment algorithms. This work aims to provide valuable insights to guide therapeutic strategies in JDM.

RMD OpenVol. 11(2)
Hospital Universitario Infanta Leonor (ES)
Good health and well-being
Openalex Percentile: Top 10%
Inflammatory Myopathies and Dermatomyositis
2.71
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