Evidence map›Paper›PMID 40465294›Full record

ArticleJAMA network open2025

Immune Checkpoint Inhibitors for Patients With Preexisting Autoimmune Neurologic Disorders.

Kylie Fletcher, Marc Machaalani, Razane El Hajj Chehade, Amin H Nassar, Rashad Nawfal, Michael Manos, Alexander M Menzies, Frank Aboubakar-Nana, Jessica C Hassel, David J Pinato and 15 more

Abstract readMulticenter Study
In one paragraph

Article in JAMA network open, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing 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

9 citing papers in PubMed.

  1. The Immune Checkpoint Inhibitors Journey: From Early Promise to Lasting Impact.Journal of immunotherapy and precision oncology · 2026
    Review
  2. Article
  3. Article
  4. Article
  5. Observational
  6. Article
  7. Review
  8. Review
  9. Review
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

25 authors.

Kylie FletcherVanderbilt University School of Medicine, Nashville, Tennessee.
Marc MachaalaniDana Farber Cancer Institute, Boston, Massachusetts.
Razane El Hajj ChehadeDana Farber Cancer Institute, Boston, Massachusetts.
Amin H NassarYale University, New Haven, Connecticut.
Rashad NawfalDana Farber Cancer Institute, Boston, Massachusetts.
Michael ManosDana Farber Cancer Institute, Boston, Massachusetts.
Alexander M MenziesMelanoma Institute Australia, The University of Sydney, Sydney, New South Wales, Australia.
Frank Aboubakar-NanaService de Pneumologie, Cliniques Universitaires Saint-Luc, Brussels, Belgium.
Jessica C HasselUniversity Hospital Heidelberg, Heidelberg, Germany.
David J PinatoDepartment of Surgery & Cancer, Imperial College London, Hammersmith Hospital, London, United Kingdom.
Alexandra JohnsonClatterbridge Cancer Centre NHS Foundation Trust, Liverpool, United Kingdom.
Anna C Olsson-BrownClatterbridge Cancer Centre NHS Foundation Trust, Liverpool, United Kingdom.
Matteo S CarlinoMelanoma Institute Australia, The University of Sydney, Sydney, New South Wales, Australia.
Andrea MalgeriFondazione Policlinico Universitario Campus-Biomedico, Roma, Italy.
Alessio CortelliniDepartment of Surgery & Cancer, Imperial College London, Hammersmith Hospital, London, United Kingdom.
Aditi SinghDepartment of Oncology, Mayo Clinic, Rochester, Minnesota.
Kaushal ParikhDepartment of Oncology, Mayo Clinic, Rochester, Minnesota.
So Yeon KimYale University, New Haven, Connecticut.
Abdul Rafeh NaqashMedical Oncology, Stephenson Cancer Center, The University of Oklahoma Health Sciences, Oklahoma City.
Georgina V LongMelanoma Institute Australia, The University of Sydney, Sydney, New South Wales, Australia.
Pavan ChallaYale University, New Haven, Connecticut.
Toni K ChoueiriDana Farber Cancer Institute, Boston, Massachusetts.
Elad SharonDana Farber Cancer Institute, Boston, Massachusetts.
Shailee ShahDepartment of Neurology, Northwestern University, Chicago, Illinois.
Douglas B JohnsonDepartment of Hematology/Oncology, Vanderbilt University Medical Center, Nashville, Tennessee.

Funding

Long-Term Cardiovascular Sequelae of Cancer ImmunotherapiesR01HL155990 · NHLBI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI JOHNSON, DOUGLAS B, MOSLEHI, JAVID J · 2021 to 2025
$3.3M
(PQ8) Patient- and tumor-specific biomarkers and mechanisms that predict irAEs resulting from checkpoint inhibitionR01CA227481 · NCI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI BALKO, JUSTIN M, JOHNSON, DOUGLAS B · 2019 to 2023
$2.6M
NCI NIH HHS R01 CA227481NHLBI NIH HHS R01 HL155990
6 · The paper itself

Abstract

Importance: Immune checkpoint inhibitors (ICIs) are efficacious in many cancer types but can produce immune-related adverse events (irAEs). As such, patients with preexisting autoimmune disorders are often excluded from clinical trials, although subsequent studies have shown that many of these patients have acceptable ICI tolerance. The safety and efficacy of ICIs among patients with preexisting neurologic autoimmune disorders (NAIDs) is not well characterized. Objective: To evaluate the safety and clinical outcomes associated with ICI therapy among patients with NAIDs. Design, Setting, and Participants: This multicenter retrospective cohort study included patients with cancer who were treated with ICIs between October 2013 and May 2023 and had preexisting multiple sclerosis (MS), myasthenia gravis (MG), Guillain-Barré syndrome (GBS), and other NAIDs as well as a control cohort of patients with Parkinson disease (PD). Exposure: ICI therapy. Main Outcomes and Measures: Demographic and clinical characteristics (neurologic disability, active or recent immunosuppression), ICI outcomes (response, progression-free survival [PFS], and overall survival [OS]), and safety outcomes (NAID exacerbation, irAEs) were collected. Results: A total of 135 patients were included; the median (range) age was 72 (40-88) years, 84 (62%) were men, and 51 (38%) were women. A total of 45 patients had MS; 18, MG; 10, GBS; 5, another NAID; and 57, PD. Exacerbations occurred most frequently in MG (12 of 18 patients [67%]), often resulting in hospitalization (6 [50%]) or death (2 [17%]), with much lower rates in the MS cohort (8 of 45 patients [18%]). Ten patients with a history of GBS tolerated ICI without exacerbations, although 1 developed a fatal case of Lambert Eaton myasthenic syndrome following ICI treatment. No differences in response rate, PFS, or OS were observed between NAID groups. Conclusions and Relevance: In this cohort study of ICI use in NAIDs, patients with MG had frequent and more severe exacerbations, while those with MS had few exacerbations. No obvious differences in survival between groups were observed. ICI may be an option for many patients with appropriate oncologic indications and preexisting NAIDs.

Indexed as

Autoimmune DiseasesAutoimmune Diseases of the Nervous SystemImmune Checkpoint InhibitorsNeoplasmsAdultAgedAged, 80 and overFemaleHumansMaleMiddle AgedRetrospective StudiesImmune Checkpoint Inhibitors

Identifiers

PMID40465294
PMCPMC12138719

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.