Failure of daratumumab in the treatment of anti-synthetase syndrome: A case report

Anti-synthetase syndrome is a subset of idiopathic inflammatory myopathies, for which refractory disease can be difficult to treat. Daratumumab, an anti-CD38 monoclonal antibody primarily used in hematologic malignancies, has recently shown promise in very few case reports of refractory idiopathic inflammatory myopathies. We present a case of a 44-year-old man with anti-Jo1 anti-synthetase syndrome with concurrent anti-Ro52, in which myositis remained refractory to multiple immunosuppressants. Despite treatment with daratumumab, the patient did not respond and ultimately succumbed to infection. This case underscores the need for further research to better define the role of daratumumab in idiopathic inflammatory myopathies and identify predictors of treatment response.

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Publication Details

Journal
SAGE Open Medical Case Reports
Published
2025-04-29
DOI
https://doi.org/10.1177/2050313x251336022
Citations
2
Primary Topic
Inflammatory Myopathies and Dermatomyositis
Type
article
Field-Weighted Citation Impact
2.71
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article

Failure of daratumumab in the treatment of anti-synthetase syndrome: A case report

Valérie Leclair, Rayan Kaedbey, Nam Nguyen, Marie Hudson
2 citations
SAGE Open Medical Case Reports
Inflammatory Myopathies and Dermatomyositis
2.71
article

Failure of daratumumab in the treatment of anti-synthetase syndrome: A case report

Valérie Leclair, Rayan Kaedbey, Nam Nguyen, Marie Hudson
article en
2 citations

Abstract

Anti-synthetase syndrome is a subset of idiopathic inflammatory myopathies, for which refractory disease can be difficult to treat. Daratumumab, an anti-CD38 monoclonal antibody primarily used in hematologic malignancies, has recently shown promise in very few case reports of refractory idiopathic inflammatory myopathies. We present a case of a 44-year-old man with anti-Jo1 anti-synthetase syndrome with concurrent anti-Ro52, in which myositis remained refractory to multiple immunosuppressants. Despite treatment with daratumumab, the patient did not respond and ultimately succumbed to infection. This case underscores the need for further research to better define the role of daratumumab in idiopathic inflammatory myopathies and identify predictors of treatment response.

SAGE Open Medical Case ReportsVol. 13
McGill University Health Centre (CA), Jewish General Hospital (CA)
Good health and well-being
Openalex Percentile: Top 11%
Inflammatory Myopathies and Dermatomyositis
2.71
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