AI Article Synopsis

  • Myasthenia gravis (MG) - Lambert-Eaton (LE) overlap syndrome, a rare condition, was identified in a patient undergoing treatment for metastatic melanoma with the drug nivolumab, an anti-PD1 inhibitor.
  • The patient experienced symptoms such as fatigue, ptosis, and swallowing difficulties after receiving nivolumab, which led to the diagnosis through various antibody tests and electromyogram findings.
  • Despite halting nivolumab and administering immunosuppressive treatment that improved the symptoms, a relapse occurred two years later, suggesting potential links between brain inflammation from radiation therapy and the onset of MG-LE overlap syndrome.

Article Abstract

Introduction: Myasthenia gravis (MG) Lambert-Eaton (LE) overlap syndrome is a rare condition. Here, we describe the first case of MG-LE overlap syndrome revealed by the anti-programmed cell death 1 inhibitor, nivolumab, in a patient treated for metastatic melanoma.

Case: Three months after receiving nivolumab and 1 month after brain metastasis radiotherapy, our patient developed generalized fatigue with intermittent ptosis and swallowing difficulty suggesting a myasthenic syndrome. Electromyogram findings, anti-acetylcholine receptor, and anti-calcium channel antibodies levels were consistent with an immune-related myasthenic syndrome with specific features for both MG and LE syndromes. Immunotherapy with nivolumab was stopped. Patient was treated with systemic immunosuppressive and anti-cholinesterase drugs, with remarkable improvement of his neurological symptoms. Prolonged partial remission was obtained for his metastatic melanoma without need for a third-line treatment. Two years later, a relapse of hismyasthenic symptoms was observed along with new neurological symptoms related to brain radiation necrosis.

Conclusion: We describe the first case of MG-LE overlap syndrome diagnosed after anti-PD1 immunotherapy for metastatic melanoma, which appeared after radiation therapy and then relapsed after brain radiation necrosis. We hypothesized a role for brain inflammation as a trigger for MG-LE onset. Neuro-muscular junctions disease induced or revealed by checkpoint inhibitors can be challenging and requires long-term follow-up.

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http://dx.doi.org/10.1007/s10072-021-05557-9DOI Listing

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