ArticleEuropean journal of neurology2026
Severe Immune-Related Neurological Adverse Events Associated With Immune Checkpoint Inhibitor Treatment: A Retrospective Single-Center Study.
Article in European journal of neurology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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Abstract
backgroundImmune checkpoint inhibitors (ICIs) have revolutionized the treatment of various malignancies. The resulting activation of the immune system may lead to neurological immune-related adverse events (n-irAEs). Here, we retrospectively characterized severe n-irAEs in a monocentric cohort.
methodsWe screened an in-house registry of the Medical University of Vienna, Austria, including all patients treated with ICIs between 2007 and 2023. Patients who underwent a neurological evaluation were identified, and their medical records were reviewed. Cases with severe (i.e., grade ≥ 3) n-irAEs were analyzed. We report clinical and demographic characteristics, neurological manifestations, treatment and outcomes.
resultsTen out of 2043 screened patients (i.e., 0.5%) developed severe n-irAEs. In most cases (n = 7), neurological manifestations involved the neuromuscular system and/or peripheral nerves, including myasthenia/myositis (n = 5), polyneuropathy (n = 1), and facial nerve palsy (n = 1). Central nervous system involvement included aseptic meningitis, myelitis, and stroke (each n = 1). The number of ICI cycles prior to n-irAE onset varied, with a median of 3 cycles (range 1-43). The median time from the last infusion to symptom onset was 7 days (range 2-24). n-irAEs led to ICI discontinuation and/or immunomodulatory treatments in 9 patients. Clinical improvement was observed in 7 of 10 cases. No deaths were attributed to ICI-related toxicity.
conclusionOur findings indicate that severe n-irAEs are rare. Nonetheless, clinicians should remain vigilant for delayed-onset neurotoxicity, even after long treatment exposure. Most patients showed clinical improvement following ICI discontinuation and/or immunomodulatory treatments.
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