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Role for long term treatment in NMOSD induced by the immune checkpoint inhibitor cemiplimab
Fien Oelbrandt1, Romain Marignier2, Bénédicte Dubois1
1Department of Neurology, University Hospitals Leuven, Leuven, Belgium.
Abstract:
We present the case of a 54-year-old patient treated with cemiplimab, an immune checkpoint inhibitor (ICI), for multiple basal cell carcinomas in the context of Gorlin Goltz syndrome. Gorlin Goltz syndrome is an autosomal dominant multisystem disorder characterized, among other features, by multiple early-onset basal cell carcinomas (BCCs). After receiving Cemiplimab, she developed aquaporin-4 antibody (AQP4-Ab) positive neuromyelitis optica spectrum disorder (NMOSD). While several case reports have documented NMOSD induced by other ICIs, this is the first case associated with cemiplimab. Although guidelines exist for the acute treatment of a first relapse of ICI-induced NMOSD, long-term management to prevent new relapses remains challenging. We believe that these patients require maintenance therapy to prevent future relapses and propose rituximab or tocilizumab as suitable options.
Insights
This case report details a patient with Gorlin Goltz syndrome who developed neuromyelitis optica spectrum disorder (NMOSD) after cemiplimab treatment. It highlights the need for long-term management strategies for immune checkpoint inhibitor-induced NMOSD.
Area of Science:
- Neuroimmunology
- Dermatology
- Oncology
Background:
- Gorlin Goltz syndrome is a genetic disorder associated with multiple basal cell carcinomas (BCCs).
- Immune checkpoint inhibitors (ICIs) like cemiplimab are used to treat advanced cancers.
- Neuromyelitis optica spectrum disorder (NMOSD) is a rare autoimmune condition affecting the central nervous system.
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