Evidence map›Paper›PMID 42227599›Full record

ArticleEuropean journal of neurology2026

Severe Immune-Related Neurological Adverse Events Associated With Immune Checkpoint Inhibitor Treatment: A Retrospective Single-Center Study.

Anna Grisold, Angelika M Starzer, Sara Silvaieh, Martin Krenn, Marie-Bernadette Aretin, Manuela Schmidinger, Julia M Ressler, Stephan Polterauer, Thomas Berger, Matthias Preusser and 1 more

Abstract read
In one paragraph

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.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors.

Anna GrisoldDepartment of Neurology, Medical University of Vienna, Vienna, Austria.ORCID https://orcid.org/0000-0002-5619-4858
Angelika M StarzerDivision of Oncology, Department of Medicine I, Medical University of Vienna, Vienna, Austria.
Sara SilvaiehDepartment of Neurology, Medical University of Vienna, Vienna, Austria.
Martin KrennDepartment of Neurology, Medical University of Vienna, Vienna, Austria.
Marie-Bernadette AretinPharmacy Department, Vienna General Hospital, Vienna, Austria.
Manuela SchmidingerDepartment of Urology, Comprehensive Cancer Center, Medical University of Vienna, Vienna, Austria.
Julia M ResslerDepartment of Dermatology, Medical University of Vienna, Vienna, Austria.ORCID https://orcid.org/0000-0001-8602-0878
Stephan PolterauerDepartment of Obstetrics and Gynecology, Comprehensive Cancer Center, Medical University of Vienna, Vienna, Austria.
Thomas BergerDepartment of Neurology, Medical University of Vienna, Vienna, Austria.ORCID https://orcid.org/0000-0001-5626-1144
Matthias PreusserDivision of Oncology, Department of Medicine I, Medical University of Vienna, Vienna, Austria.
Anna S BerghoffDivision of Oncology, Department of Medicine I, Medical University of Vienna, Vienna, Austria.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

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.

Indexed as

Immune Checkpoint InhibitorsNervous System DiseasesAdultAgedAged, 80 and overFemaleHumansMaleMiddle AgedNeoplasmsRetrospective StudiesImmune Checkpoint Inhibitorsadverse eventsimmune checkpoint inhibitorneurologicaln‐irAEPD‐1PD‐L1

Identifiers

PMID42227599
PMCPMC13239952

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.