Evidence map›Paper›PMID 31989585›Full record

ReviewClinical and experimental immunology2020

Mechanisms of checkpoint inhibition-induced adverse events.

P Urwyler, I Earnshaw, M Bermudez, E Perucha, W Wu, S Ryan, L Mcdonald, S N Karagiannis, L S Taams, N Powell and 2 more

Open access · bronzeAbstract readReview
In one paragraph

Review in Clinical and experimental immunology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed, 1 pooled it
2.9field-weighted citation impact, top 7% 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.

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

28 citing papers in PubMed, 1 synthesis or guideline pooled it, 50 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Organ-specific accuracy of [Japanese journal of radiology · 2024
    Article
  9. Article
  10. Article
  11. Article
  12. Review
  13. Article
  14. Article
  15. Non-invasive Detection of Immunotherapy-Induced Adverse Events.Clinical cancer research : an official journal of the American Association for Cancer Research · 2021
    Article
  16. Review
  17. Inflammatory markers in autoimmunity induced by checkpoint inhibitors.Journal of cancer research and clinical oncology · 2021
    Article
  18. Review
  19. An update on the pathogenesis of Hashimoto's thyroiditis.Journal of endocrinological investigation · 2021
    Review
  20. 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

12 authors at 2 institutions in 1 country.

P Urwyler *Department of Medical Oncology, Guy's and St Thomas' NHS Foundation Trust, London, UK.
I Earnshaw *Centre for Inflammation Biology and Cancer Immunology, Department of Inflammatory Biology, School of Immunology and Microbial Sciences, Faculty of Life Sciences and Medicine, King's College London, London, UK.
M Bermudez *Centre for Inflammation Biology and Cancer Immunology, Department of Inflammatory Biology, School of Immunology and Microbial Sciences, Faculty of Life Sciences and Medicine, King's College London, London, UK.
E PeruchaCentre for Inflammation Biology and Cancer Immunology, Department of Inflammatory Biology, School of Immunology and Microbial Sciences, Faculty of Life Sciences and Medicine, King's College London, London, UK.
W WuCentre for Inflammation Biology and Cancer Immunology, Department of Inflammatory Biology, School of Immunology and Microbial Sciences, Faculty of Life Sciences and Medicine, King's College London, London, UK.
S RyanCentre for Inflammation Biology and Cancer Immunology, Department of Inflammatory Biology, School of Immunology and Microbial Sciences, Faculty of Life Sciences and Medicine, King's College London, London, UK.
L McdonaldOncology and Haematology Clinical Trials, Guy's and St Thomas' NHS Foundation Trust, London, UK.
S N KaragiannisSt John's Institute of Dermatology, School of Basic and Medical Biosciences, King's College London, London, UK.ORCID 0000-0002-4100-7810
L S TaamsCentre for Inflammation Biology and Cancer Immunology, Department of Inflammatory Biology, School of Immunology and Microbial Sciences, Faculty of Life Sciences and Medicine, King's College London, London, UK.ORCID 0000-0002-9337-7194
N PowellCentre for Inflammation Biology and Cancer Immunology, Department of Inflammatory Biology, School of Immunology and Microbial Sciences, Faculty of Life Sciences and Medicine, King's College London, London, UK.
A CopeCentre for Inflammation Biology and Cancer Immunology, Department of Inflammatory Biology, School of Immunology and Microbial Sciences, Faculty of Life Sciences and Medicine, King's College London, London, UK.
S PapaDepartment of Medical Oncology, Guy's and St Thomas' NHS Foundation Trust, London, UK.ORCID 0000-0002-9063-7675
King's College London · GBGuy's and St Thomas' NHS Foundation Trust · GB

Funding

Medical Research Council MR/L023091/1
6 · The paper itself

Abstract

Immune checkpoint inhibition has revolutionized the treatment of several solid cancers, most notably melanoma and non-small-cell lung cancer (NSCLC). Drugs targeting cytotoxic T lymphocyte antigen (CTLA)-4 and programmed cell death 1 (PD-1) have made their way into routine clinical use; however, this has not been without difficulties. Stimulation of the immune system to target cancer has been found to result in a reduction of self-tolerance, leading to the development of adverse effects that resemble autoimmunity. These adverse effects are erratic in their onset and severity and can theoretically affect any organ type. Several mechanisms for immune-related toxicity have been investigated over recent years; however, no consensus on the cause or prediction of toxicity has been reached. This review seeks to examine reported evidence for possible mechanisms of toxicity, methods for prediction of those at risk and a discussion of future prospects within the field.

Indexed as

Antineoplastic AgentsCarcinoma, Non-Small-Cell LungCTLA-4 AntigenLung NeoplasmsNeoplasm ProteinsProgrammed Cell Death 1 ReceptorHumansAntineoplastic AgentsCTLA-4 AntigenCTLA4 protein, humanNeoplasm ProteinsPDCD1 protein, humanProgrammed Cell Death 1 ReceptorcancercheckpointCTLA-4immunotherapyPD-1

Identifiers

PMID31989585
PMCPMC7160658
OpenAlexW3004211126

What OpenQuestion holds

Textmetadata
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.