The Use of Rituximab in the Management of Refractory Dermatomyositis
February 2017 | Volume 16 | Issue 2 | Original Article | 162 | Copyright © 2017
Ifedayo O. Kuye BAa and Gideon P. Smith MD PhDb
aHarvard Medical School, Boston, MA bMassachusetts General Hospital, Boston, MA
There is growing adoption of rituximab in the treatment of dermatomyositis patients whose disease is refractory to steroids. However, the effects have not been extensively studied. This is a retrospective study of 25 patients with dermatomyositis who were treated with rituximab. Data from January 2000 to July 2014 was obtained from a clinical data repository, which yielded results from two tertiary centers in the United States. We analyzed information on muscle weakness, skin disease, enzyme levels, and immunosuppressive medication use before and after treatment with rituximab. The follow-up time was six months. Among the patients with skin disease before treatment with rituximab, 72.2% had a clinical improvement in their skin disease at the follow-up visit (P less than0.01). Among the patients with proximal muscle weakness before treatment with rituximab, 81.8% had clinical improvement in their symptoms at the follow-up visit (P less than0.01). The average prednisone dose before rituximab therapy was 18.9 mg, and this dropped to 11.0 mg at follow up (P less than 0.05). The average number of immunosuppressive medications taken by patients dropped from 2.04 to 1.74 (P less than0.05). These changes were less in magnitude and significance among the subset of patient that had an additional connective tissue autoimmune condition.
J Drugs Dermatol. 2017;16(2):162-166.
Purchase Original Article
Purchase a single fully formatted PDF of the original manuscript as it was published in the JDD.
Download the original manuscript as it was published in the JDD.
Contact a member of the JDD Sales Team to request a quote or purchase bulk reprints, e-prints or international translation requests.
To get access to JDD's full-text articles and archives, upgrade here.
Save an unformatted copy of this article for on-screen viewing.
Print the full-text of article as it appears on the JDD site.→ proceed | ↑ close
Dermatomyositis is an idiopathic inflammatory myopathy. In its classic form, it presents with muscle weakness and cutaneous findings, although an amyopathic form also exists. The heliotrope rash and Grotton’s papules are pathognomonic cutaneous features of dermatomyositis.1 Other cutaneous features include scalp pruritus, hip and thigh erythema (holster sign), photosensitive poikilodermatous eruption (shawl sign), violaceous erythema on the extensor surfaces, and periungual and cuticular fraying (Samitz sign).1 In addition patients may have calcinosis. Patients can also have multi-organ system involvement including most commonly pulmonary fibrosis and hypertension, but also oesophageal disease, arthritis, and cardiac dysfunction.1The mainstay of therapy for dermatomyositis has traditionally consisted of systemic corticosteroids, especially in early muscle prominent disease.1,2 However, 25% of patients with dermatomyositis do not respond to steroids and 25-50% develop adverse reactions.1,2 In addition, long term steroid therapy has significant adverse risks. Therefore, steroid-sparing agents are often needed.There is growing evidence that rituximab may be an effective therapy in patients whose disease is refractory to steroids.3-7 Although, some studies have found limited results.8,9 Rituximab is a chimeric murine human monoclonal antibody that is directed against the CD20 antigen expressed on B cells.10 Although the pathogenesis of dermatomyositis is poorly understood, it is thought that humoral-mediated complement activation leads to the inflammation of endothelial cells, which allows activated T cells to migrate to muscle and cause ischemia.11 Thus rituximab may act to decrease the B-cell production of the autoantibodies. This study is a retrospective review of cases to evaluate the effect of rituximab on the cutaneous and muscle manifestations of dermatomyositis.
This study was approved under MGH IRB (Protocol 2014P001402). We used the Partners Healthcare Research Patient Data Registry (RPDR) to identify patients with at least one ICD-9 diagnostic code of dermatomyositis and who had been treated with rituximab between January 2000 and July 2014.Each medical record was reviewed by the authors in order ensure that the patient had a rheumatologist or dermatologist confirmed diagnosis of dermatomyositis and the patient had received rituximab specifically for the treatment of this condition. To determine baseline characteristics, we reviewed medical records from the visits immediately prior to treatment with rituximab. We recorded immunosuppressive medications and laboratory results. Muscle weakness was noted, if it was described in the medical record. The presence of skin disease was noted if the medical records described skin disease consistent with dermatomyositis. If a patient was seen by both a