Evidence map›Paper›PMID 31816085›Full record

ReviewRheumatology (Oxford, England)2019

Toxicities associated with checkpoint inhibitors-an overview.

Laura Spiers, Nicholas Coupe, Miranda Payne

Abstract readReview
In one paragraph

Review in Rheumatology (Oxford, England), 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 56 papers.

0numbers the graph read from it
0cells of the map it votes in
56citing 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

56 citing papers in PubMed.

  1. Trial
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  14. Skin Infiltrate Composition as a Telling Measure of Responses to Checkpoint Inhibitors.JID innovations : skin science from molecules to population health · 2023
    Article
  15. Article
  16. Article
  17. Article
  18. Review
  19. Article
  20. CMTM6 as a master regulator of PD-L1.Cancer immunology, immunotherapy : CII · 2022
    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

3 authors.

Laura SpiersDepartment of Oncology, Churchill Hospital, Oxford University Hospitals Foundation Trust, Oxford, UK.
Nicholas CoupeDepartment of Oncology, Churchill Hospital, Oxford University Hospitals Foundation Trust, Oxford, UK.
Miranda PayneDepartment of Oncology, Churchill Hospital, Oxford University Hospitals Foundation Trust, Oxford, UK.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Immunotherapy has an increasing role in the management of cancer, both in metastatic disease and as an adjuvant therapy. However, sensitization of the immune system with checkpoint inhibitors comes with a unique side effect profile. Full appreciation of this can take some time to emerge as some adverse events are rare, or can be subtle and potentially overlooked. Clinician awareness of these side effects can be particularly important in patients with pre-existing autoimmune conditions. Here we describe common symptoms and diagnostic strategies for organ-specific side effects of anti-CTLA-4 and anti-PD-1/PD-L1 immunotherapy agents.

Indexed as

Antineoplastic Agents, ImmunologicalChemical and Drug Induced Liver InjuryCTLA-4 AntigenDrug EruptionsEndocrine System DiseasesGastrointestinal DiseasesHumansImmunologic FactorsImmunotherapyIpilimumabNeoplasmsNervous System DiseasesProgrammed Cell Death 1 ReceptorRheumatic DiseasesAntineoplastic Agents, ImmunologicalCTLA-4 AntigenCTLA4 protein, humanImmunologic FactorsIpilimumabPDCD1 protein, humanProgrammed Cell Death 1 Receptoradverse eventcheckpoint inhibitor

Identifiers

PMID31816085
PMCPMC6900917

What OpenQuestion holds

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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.