Evidence map›Paper›PMID 35086945›Full record

ReviewJournal for immunotherapy of cancer2022

Potential therapies for immune-related adverse events associated with immune checkpoint inhibition: from monoclonal antibodies to kinase inhibition.

Meagan-Helen Henderson Berg, Sonia Victoria Del Rincón, Wilson H Miller

Registry-linked trialOpen access · goldAbstract readReview
In one paragraph

Review in Journal for immunotherapy of cancer, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT07249060 (Interferon Signature in Cancer Patients Treated With Anti-CTLA-4 and Anti-PD-1/PD-L1 Therapies), which is not on this map. Cited by 34 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed, 2 pooled it
4.5field-weighted citation impact, top 4% of its field
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.

NCT07249060 recruitingnot on this mapstarted 2024, after this paper: background citation

Interferon Signature in Cancer Patients Treated With Anti-CTLA-4 and Anti-PD-1/PD-L1 Therapies: A Multicenter, Prospective, Observational Cohort Study Comparing Cancer Patients and Non-Cancer Patients With Systemic Autoimmune Diseases

Typeobservational_patient_registrySponsorHospital Universitario ArabaRan2024 to 2026Enrolled300ConditionsImmune-Related Adverse Events, Lupus Erythematosus, Systemic, Sjogren Syndrome, Systemic Sclerosis (SSc)ArmsImmune Checkpoint Inhibitors
3 · Its place in the literature

Who cites it

34 citing papers in PubMed, 2 syntheses or guidelines pooled it, 45 citations in OpenAlex.

  1. Systemic treatment of immune checkpoint inhibitor-induced psoriasis: Inference-based guidance.Journal of the European Academy of Dermatology and Venereology : JEADV · 2025
    Pooled it
  2. Guideline
  3. Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Review
  12. Review
  13. Clinical management of checkpoint inhibitor pneumonitis: Focus, challenges, and future directions.Chinese medical journal pulmonary and critical care medicine · 2025
    Review
  14. Article
  15. Review
  16. [Immune-related severe pneumonia: A case report].Beijing da xue xue bao. Yi xue ban = Journal of Peking University. Health sciences · 2024
    Article
  17. Review
  18. Article
  19. Article
  20. 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

3 authors at 1 institution in 1 country.

Meagan-Helen Henderson BergDivision of Dermatology, McGill University, Montreal, Québec, Canada.ORCID 0000-0002-4622-2931
Sonia Victoria Del Rincón *Division of Experimental Medicine, McGill University, Montreal, Québec, Canada wilsonmiller@gmail.com sonia.delrincon@mcgill.ca.
Wilson H Miller *Division of Experimental Medicine, McGill University, Montreal, Québec, Canada wilsonmiller@gmail.com sonia.delrincon@mcgill.ca.
Jewish General Hospital · CA

Funding

CIHR MOP-142281CIHR PJT-156269CIHR PJT-162260
6 · The paper itself

Abstract

The therapeutic benefits of immune checkpoint inhibitors (ICIs), which enable antitumor immune responses, can be tempered by unwanted immune-related adverse events (irAEs). Treatment recommendations stratified by irAE phenotype and immunohistopathological findings have only recently been proposed and are often based on those used in primary autoimmune diseases, including targeting of specific proinflammatory cytokines with monoclonal antibodies. Increasing evidence supports the use of such antibody-based strategies as effective steroid-sparing treatments, although the therapies themselves may be associated with additional drug toxicities and reduced ICI efficacy. Kinases are key contributors to the adaptive and innate responses that drive primary autoimmune diseases and irAEs. The janus kinase/signal transducer and activator of transcription, Bruton's tyrosine kinase, and mitogen-activated protein kinase-interacting serine/threonine protein kinases 1 and 2 pathways are also critical to tumor progression and have important roles in cells of the tumor microenvironment. Herein, we review the histopathological, biological, and clinical evidence to support specific monoclonal antibodies and kinase inhibition as management strategies for irAEs.

Indexed as

Agammaglobulinaemia Tyrosine KinaseAntibodies, MonoclonalAutoimmune DiseasesCytokinesHumansImmune Checkpoint InhibitorsJanus Kinase InhibitorsNeoplasmsProtein Kinase InhibitorsSTAT Transcription FactorsTumor MicroenvironmentAgammaglobulinaemia Tyrosine KinaseAntibodies, MonoclonalBTK protein, humanCytokinesImmune Checkpoint InhibitorsJanus Kinase InhibitorsProtein Kinase InhibitorsSTAT Transcription Factorsautoimmunityimmunotherapyinflammationinvestigationalreviewtherapies

Identifiers

PMID35086945
PMCPMC8796266
OpenAlexW4210690867

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

Registered trials

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.