Recent developments on treatment strategies and the prognosis of dermatomyositis: a review

Dermatomyositis is an autoimmune disease affecting both skin and muscle. Steroids are the first line treatment. However, no consensus regarding dosing, length of treatment, tapering speed, or when to add which immunosuppressant in case of steroid resistance, has been reached, as randomized-controlle...

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Main Authors: Verena Isak, Joseph L. Jorizzo
Format: Article
Language:English
Published: Taylor & Francis Group 2018-07-01
Series:Journal of Dermatological Treatment
Subjects:
Online Access:http://dx.doi.org/10.1080/09546634.2017.1403549
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author Verena Isak
Joseph L. Jorizzo
author_facet Verena Isak
Joseph L. Jorizzo
author_sort Verena Isak
collection DOAJ
description Dermatomyositis is an autoimmune disease affecting both skin and muscle. Steroids are the first line treatment. However, no consensus regarding dosing, length of treatment, tapering speed, or when to add which immunosuppressant in case of steroid resistance, has been reached, as randomized-controlled trials are scarce. Especially data on long-term treatment is lacking in order to decide on the most effective treatment for long-term remission. Empiric evidence suggests that with an initially aggressive treatment with oral steroids followed by a slow taper, during which disease activity is adequately controlled, patients can be off therapy within typically 24–48 months, and remain disease-free without medication for over 20 years. Biologics such as rituximab have shown good results in the treatment of refractory DM. New, targeted therapies have been reported to improve DM in single cases or case series, but have to be evaluated for efficacy in randomized controlled trials.
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spelling doaj.art-5e12c77820e144588fa37020d5db73022023-09-15T14:08:31ZengTaylor & Francis GroupJournal of Dermatological Treatment0954-66341471-17532018-07-0129545045910.1080/09546634.2017.14035491403549Recent developments on treatment strategies and the prognosis of dermatomyositis: a reviewVerena Isak0Joseph L. Jorizzo1Winston SalemWinston SalemDermatomyositis is an autoimmune disease affecting both skin and muscle. Steroids are the first line treatment. However, no consensus regarding dosing, length of treatment, tapering speed, or when to add which immunosuppressant in case of steroid resistance, has been reached, as randomized-controlled trials are scarce. Especially data on long-term treatment is lacking in order to decide on the most effective treatment for long-term remission. Empiric evidence suggests that with an initially aggressive treatment with oral steroids followed by a slow taper, during which disease activity is adequately controlled, patients can be off therapy within typically 24–48 months, and remain disease-free without medication for over 20 years. Biologics such as rituximab have shown good results in the treatment of refractory DM. New, targeted therapies have been reported to improve DM in single cases or case series, but have to be evaluated for efficacy in randomized controlled trials.http://dx.doi.org/10.1080/09546634.2017.1403549dermatomyositisinflammatory myopathysystemic steroidsimmunosuppressants
spellingShingle Verena Isak
Joseph L. Jorizzo
Recent developments on treatment strategies and the prognosis of dermatomyositis: a review
Journal of Dermatological Treatment
dermatomyositis
inflammatory myopathy
systemic steroids
immunosuppressants
title Recent developments on treatment strategies and the prognosis of dermatomyositis: a review
title_full Recent developments on treatment strategies and the prognosis of dermatomyositis: a review
title_fullStr Recent developments on treatment strategies and the prognosis of dermatomyositis: a review
title_full_unstemmed Recent developments on treatment strategies and the prognosis of dermatomyositis: a review
title_short Recent developments on treatment strategies and the prognosis of dermatomyositis: a review
title_sort recent developments on treatment strategies and the prognosis of dermatomyositis a review
topic dermatomyositis
inflammatory myopathy
systemic steroids
immunosuppressants
url http://dx.doi.org/10.1080/09546634.2017.1403549
work_keys_str_mv AT verenaisak recentdevelopmentsontreatmentstrategiesandtheprognosisofdermatomyositisareview
AT josephljorizzo recentdevelopmentsontreatmentstrategiesandtheprognosisofdermatomyositisareview