Evidence map›Paper›PMID 39066587›Full record

ArticleThe oncologist2025

Immune-related encephalitis after immune checkpoint inhibitor therapy.

Monica W Buckley, Aanika Balaji Warner, Julie Brahmer, Laura C Cappelli, William H Sharfman, Ephraim Fuchs, Hyunseok Kang, Patrick M Forde, Douglas E Gladstone, Richard Ambinder and 10 more

Abstract read
In one paragraph

Article in The oncologist, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing 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

17 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Review
  13. Article
  14. Article
  15. Review
  16. Review
  17. Article
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

20 authors.

Monica W BuckleyDepartment of Neurology, Johns Hopkins University School of Medicine, Baltimore, MD 21287, United States.
Aanika Balaji WarnerDepartment of Oncology, Johns Hopkins University School of Medicine, Baltimore, MD 21287, United States.ORCID 0000-0001-6697-3364
Julie BrahmerDepartment of Oncology, Johns Hopkins University School of Medicine, Baltimore, MD 21287, United States.
Laura C CappelliDepartment of Oncology, Johns Hopkins University School of Medicine, Baltimore, MD 21287, United States.
William H SharfmanDepartment of Oncology, Johns Hopkins University School of Medicine, Baltimore, MD 21287, United States.
Ephraim FuchsDepartment of Oncology, Johns Hopkins University School of Medicine, Baltimore, MD 21287, United States.
Hyunseok KangDepartment of Oncology, Johns Hopkins University School of Medicine, Baltimore, MD 21287, United States.
Patrick M FordeDepartment of Oncology, Johns Hopkins University School of Medicine, Baltimore, MD 21287, United States.
Douglas E GladstoneDepartment of Oncology, Johns Hopkins University School of Medicine, Baltimore, MD 21287, United States.
Richard AmbinderDepartment of Oncology, Johns Hopkins University School of Medicine, Baltimore, MD 21287, United States.
Ronan J KellyDepartment of Oncology, Johns Hopkins University School of Medicine, Baltimore, MD 21287, United States.
Evan J LipsonDepartment of Oncology, Johns Hopkins University School of Medicine, Baltimore, MD 21287, United States.ORCID 0000-0003-2976-0911
Ivana GojoDepartment of Oncology, Johns Hopkins University School of Medicine, Baltimore, MD 21287, United States.
Edward J LeeMaryland Oncology Hematology, Columbia, MD 21044, United States.
Tory P JohnsonDepartment of Neurology, Johns Hopkins University School of Medicine, Baltimore, MD 21287, United States.
Shiv SaidhaDepartment of Neurology, Johns Hopkins University School of Medicine, Baltimore, MD 21287, United States.
Rafael LlinasDepartment of Neurology, Johns Hopkins University School of Medicine, Baltimore, MD 21287, United States.
Lyle W OstrowDepartment of Neurology, Johns Hopkins University School of Medicine, Baltimore, MD 21287, United States.
Jarushka NaidooDepartment of Oncology, Johns Hopkins University School of Medicine, Baltimore, MD 21287, United States.
John C ProbascoDepartment of Neurology, Johns Hopkins University School of Medicine, Baltimore, MD 21287, United States.ORCID 0000-0003-2095-0786

Funding

Translational Research Central ServicesP30CA006973 · NCI · JOHNS HOPKINS UNIVERSITY · PI Rosalie Wollett · 1985 to 2026
$208.6M
AbbVieAmgenAstraZenecaBayerBiogenBristol-Myers SquibbCelgeneEMD SeronoNCI NIH HHS P30 CA006973
6 · The paper itself

Abstract

backgroundImmune checkpoint inhibitors (ICI) have revolutionized cancer treatment but can trigger immune-related encephalitis. We report one of the largest case series of patients with immune-related encephalitis and review of the literature.

methodsRetrospective series of patients with immune-related encephalitis and literature review.

resultsFourteen patients with cancer treated with ICI (50% combination therapy) developed immune-related encephalitis. Diagnostic testing revealed cerebral spinal fluid (CSF) lymphocytic pleocytosis (85%) and elevated protein (69%), abnormal brain magnetic resonance imaging(MRI) (33%) or brain FDG-PET (25%), electroencephalogram (EEG) abnormalities (30%), and autoantibodies (31%). Encephalitis treatment included: corticosteroids (86%), intravenous immunoglobulin (IVIg) (36%), plasmapheresis (7%), and rituximab (29%). There were no deaths and 12 patients had significant recovery, although long-term complications were observed. All patients discontinued ICI. Longitudinal follow-up demonstrated anti-cancer response to ICI at 3 months (85%) and 6 months post-ICI initiation (77%). A literature review identified 132 patients with immune-related encephalitis. Most were treated with PD-1 inhibitors (18% combination). Common abnormalities included elevated CSF protein (84%) or pleocytosis (77%), abnormal brain MRI (65%), or autoantibodies (47%). Nearly all were treated with corticosteroids, many required additional therapy with IVIg (26%) or rituximab (12%). Most patients had clinical improvement (81%) but a minority (10%) had a clinical relapse after completing corticosteroid taper. ICIs were resumed in 7 patients (5%), with relapse in 3. CONCLUSIONS AND RELEVANCE: Immune-related encephalitis is treatable and improves with corticosteroids in most cases but may require additional immunosuppression. Re-emergence of encephalitis is rare and does not typically result in adverse outcomes, and this should be considered in neurological immune-related adverse event management guidelines.

Indexed as

EncephalitisImmune Checkpoint InhibitorsNeoplasmsAdultAgedAged, 80 and overFemaleHumansMaleMiddle AgedRetrospective StudiesImmune Checkpoint Inhibitorsautoimmunecancerencephalitisimmune checkpoint

Identifiers

PMID39066587
PMCPMC11783331

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.