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Immune Checkpoint Inhibitor-Induced Ocular Myasthenia Gravis: Case Series and Literature Review
Victoria A Dezard1, Heather M McDonald, Wayne T Cornblath
1Department of Medicine (VD), Université de Sherbrooke, Sherbrooke, Canada; Department of Ophthalmology and Visual Sciences (HMM, EM), University of Toronto, Toronto, Canada; Departments of Ophthalmology and Visual Sciences (WC) and Neurology (WC), University of Michigan, Ann Arbor, Michigan; and Division of Neurology (EM), Department of Medicine, University of Toronto, Toronto, Canada.
Immune checkpoint inhibitor-induced ocular myasthenia gravis (ICI-OMG) is rare, presenting with ptosis and diplopia. Diagnosis is challenging, and treatments show mixed results, often leading to chronic symptoms.
Area of Science:
- Neuro-ophthalmology
- Oncology
- Immunology
Background:
- Immune checkpoint inhibitors (ICIs) enhance anti-cancer immunity but can cause immune-related adverse events.
- ICI-induced myasthenia gravis (ICI-MG) is a known side effect, with limited data on the isolated ocular form (ICI-OMG).
Purpose of the Study:
- To characterize the clinical presentation of patients with ICI-OMG.
- To evaluate treatment responses in ICI-OMG cases.
Main Methods:
- A case series of patients with ICI-OMG from neuro-ophthalmology practices.
- A comprehensive literature review of published ICI-OMG cases.
Main Results:
- Identified 3 new cases and reviewed 12 additional cases of ICI-OMG, predominantly associated with pembrolizumab.
- All patients presented with ptosis; most had diplopia. Antibody tests and sfEMG results were often inconclusive.
- Treatments including corticosteroids and IVIg yielded variable responses.
Conclusions:
- ICI-OMG is a rare condition with diagnostic challenges due to unreliable testing.
- Early recognition is vital; however, patients often experience chronic symptoms with incomplete recovery.
- Further research is needed for improved diagnostic markers and therapeutic strategies.
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