Evidence map›Paper›PMID 41348123›Full record

ReviewRadiologie (Heidelberg, Germany)2026

[Imaging of neurological adverse events associated with immunotherapies : Immune checkpoint inhibitors and CAR-T cells].

Timotheus Josef Neumann, Anna Magdalena Baz, Elena Nicola Charlotte Schmidt, Zeynep Bendella, Ralf Clauberg, Alexander Radbruch, Anne-Katrin Pröbstel, Antje Bischof, Nora Möhn, Barbara Daria Wichtmann

Abstract readEnglish AbstractReview
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In one paragraph

Review in Radiologie (Heidelberg, Germany), 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

10 authors.

Timotheus Josef NeumannKlinik für Diagnostische und Interventionelle Neuroradiologie und Kinderneuroradiologie, Universitätsklinikum Bonn, Venusberg-Campus 1, 53127, Bonn, Deutschland.
Anna Magdalena BazKlinik für Diagnostische und Interventionelle Neuroradiologie und Kinderneuroradiologie, Universitätsklinikum Bonn, Venusberg-Campus 1, 53127, Bonn, Deutschland.
Elena Nicola Charlotte SchmidtKlinik für Diagnostische und Interventionelle Neuroradiologie und Kinderneuroradiologie, Universitätsklinikum Bonn, Venusberg-Campus 1, 53127, Bonn, Deutschland.
Zeynep BendellaKlinik für Diagnostische und Interventionelle Neuroradiologie und Kinderneuroradiologie, Universitätsklinikum Bonn, Venusberg-Campus 1, 53127, Bonn, Deutschland.
Ralf ClaubergKlinik für Diagnostische und Interventionelle Neuroradiologie und Kinderneuroradiologie, Universitätsklinikum Bonn, Venusberg-Campus 1, 53127, Bonn, Deutschland.
Alexander RadbruchKlinik für Diagnostische und Interventionelle Neuroradiologie und Kinderneuroradiologie, Universitätsklinikum Bonn, Venusberg-Campus 1, 53127, Bonn, Deutschland.
Anne-Katrin PröbstelKlinik für Neuroimmunologie, Zentrum für Neurologie, Universitätsklinikum Bonn, Bonn, Deutschland.
Antje BischofKlinik für Neuroimmunologie, Zentrum für Neurologie, Universitätsklinikum Bonn, Bonn, Deutschland.
Nora MöhnKlinik für Neuroimmunologie, Zentrum für Neurologie, Universitätsklinikum Bonn, Bonn, Deutschland.
Barbara Daria WichtmannKlinik für Diagnostische und Interventionelle Neuroradiologie und Kinderneuroradiologie, Universitätsklinikum Bonn, Venusberg-Campus 1, 53127, Bonn, Deutschland. barbara.wichtmann@ukbonn.de.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundImmune checkpoint inhibitors (ICI) and chimeric antigen receptor T‑cell (CAR-T) therapies have fundamentally transformed oncology. With their increasing use, immune-related adverse events (irAEs) have gained attention, including those affecting the nervous system.

objectivesTo describe the clinical and imaging characteristics of neurological immune-related adverse events (NirAEs) under ICI and CAR‑T therapy, as well as their differential diagnostic and therapeutic implications. MATERIALS AND

methodsReview of current literature on the incidence, clinical spectrum, and imaging features of NirAEs.

resultsNirAEs occur in approximately 1-6% of patients treated with ICIs. Common manifestations include myositis, myasthenic syndromes, peripheral neuropathies, and various forms of encephalitis, which may differ clinically and radiologically from their idiopathic or paraneoplastic counterparts. Under CAR‑T therapy, immune effector cell-associated neurotoxicity syndrome (ICANS) represents the most frequent neurotoxic complication and affects about 30% of patients. Magnetic resonance imaging (MRI) is the imaging modality of choice but often reveals nonspecific or initially unremarkable findings. A pretherapeutic baseline MRI and close imaging follow-up improve diagnostic interpretation and prognostic assessment. Findings must always be interpreted within the clinical context and through interdisciplinary collaboration.

conclusionNirAEs are rare but potentially life-threatening. Due to unspecific imaging findings and overlapping differential diagnoses, close interdisciplinary cooperation between radiology, neurology, and oncology is essential. Early recognition and imaging follow-up are key to improving prognosis and survival.

Indexed as

Immune Checkpoint InhibitorsImmunotherapyImmunotherapy, AdoptiveMagnetic Resonance ImagingNervous System DiseasesNeurotoxicity SyndromesDiagnosis, DifferentialHumansReceptors, Chimeric AntigenImmune Checkpoint InhibitorsReceptors, Chimeric AntigenCentral and peripheral nervous systemICANS (immune effector cell–associated neurotoxicity syndrome)Magnetic resonance imagingNeuroradiological diagnosticsNeurotoxicity under immunotherapy

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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.