Acute leukoencephalopathy associated with daratumumab treatment in POEMS syndrome: a case report

Daratumumab, a monoclonal antibody against CD38, is increasingly used in the treatment of multiple myeloma, other hematological malignancies and autoimmune diseases. Little is known about its CNS toxicity. We present a case of a patient with POEMS syndrome (syndrome of polyneuropathy, organomegaly,...

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Veröffentlicht in:Frontiers in immunology Jg. 15; S. 1451693
Hauptverfasser: Steinegger, Lukas, Nierobisch, Nathalie, De Vere-Tyndall, Anthony, Schreiner, Bettina, Roth, Patrick, Kappos, Ludwig, Kana, Veronika, Herwerth, Marina
Format: Journal Article
Sprache:Englisch
Veröffentlicht: Switzerland Frontiers Media SA 26.09.2024
Frontiers Media S.A
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ISSN:1664-3224, 1664-3224
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Zusammenfassung:Daratumumab, a monoclonal antibody against CD38, is increasingly used in the treatment of multiple myeloma, other hematological malignancies and autoimmune diseases. Little is known about its CNS toxicity. We present a case of a patient with POEMS syndrome (syndrome of polyneuropathy, organomegaly, endocrinopathy, monoclonal gammopathy and skin changes) who developed an acute leukoencephalopathy shortly after initiation of therapy with daratumumab. Case report following the CARE case report guidelines. The patient presented with symptoms of headache and diffuse worsening of a pre-existing tetraparesis. MRI showed a rapidly progressive leukoencephalopathy. Extensive diagnostic evaluation revealed no specific cause, suggesting the leukoencephalopathy to be caused by daratumumab. Our report highlights a probably rare, but clinically significant adverse effect of daratumumab and underlines the necessity of raised vigilance for neurological side effects in patients treated with daratumumab.
Bibliographie:SourceType-Scholarly Journals-1
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ObjectType-Case Study-2
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Reviewed by: Ronald Antulov, University Hospital of Southern Denmark, Denmark
Edited by: Philipp Albrecht, Heinrich Heine University of Düsseldorf, Germany
Noriyuki Matsukawa, Nagoya City University, Japan
ISSN:1664-3224
1664-3224
DOI:10.3389/fimmu.2024.1451693