Evidence map›Paper›PMID 30006825›Full record

ReviewTargeted oncology2018

Coronary Toxicities of Anti-PD-1 and Anti-PD-L1 Immunotherapies: a Case Report and Review of the Literature and International Registries.

Marion Ferreira, Eric Pichon, Delphine Carmier, Emilie Bouquet, Cécile Pageot, Theodora Bejan-Angoulvant, Marion Campana, Emmanuelle Vermes, Sylvain Marchand-Adam

Abstract readCase ReportsReview
PubMed Publisher
In one paragraph

Review in Targeted oncology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
2.2field-weighted citation impact, top 9% 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

15 citing papers in PubMed, 40 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Immune checkpoint inhibitors and potential risk of thromboembolic events: Analysis of the WHO global database of individual case safety reports.Saudi pharmaceutical journal : SPJ : the official publication of the Saudi Pharmaceutical Society · 2022
    Article
  6. Article
  7. Review
  8. Review
  9. Review
  10. Review
  11. Review
  12. Article
  13. Article
  14. Observational
  15. 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

9 authors at 2 institutions in 2 countries.

Marion FerreiraDepartment of Pneumology and Respiratory Functional Exploration, University Hospital of Tours, Tours, France. marion-ferreira@hotmail.fr.ORCID 0000-0001-6311-0256
Eric PichonDepartment of Pneumology and Respiratory Functional Exploration, University Hospital of Tours, Tours, France.
Delphine CarmierDepartment of Pneumology and Respiratory Functional Exploration, University Hospital of Tours, Tours, France.
Emilie BouquetDepartment of Clinical Pharmacology and Regional Pharmacovigilance Center, University Hospital of Tours, Tours, France.
Cécile PageotRegional Pharmacovigilance Center of Bordeaux, Bordeaux, France.
Theodora Bejan-AngoulvantMedical Pharmacology Department, University Hospital of Tours, Tours, France.
Marion CampanaDepartment of Pneumology and Respiratory Functional Exploration, University Hospital of Tours, Tours, France.
Emmanuelle VermesDepartment of Radiology, University Hospital of Tours, Tours, France.
Sylvain Marchand-AdamDepartment of Pneumology and Respiratory Functional Exploration, University Hospital of Tours, Tours, France.
Université de Tours · FRBordeaux Population Health · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Immunotherapy medications that target programmed death 1 protein (PD-1) and programmed death-ligand 1 (PD-L1), such as nivolumab, pembrolizumab, and atezolizumab, are currently used in the first- or second-line treatment of non-small cell lung cancers, among other indications. However, these agents are associated with immune-related side effects, the most common of which are endocrinopathies, colitis, hepatitis, and interstitial pneumonitis. In contrast, coronary toxicities are rarely reported and remain poorly understood. Here, we describe the case of a patient who developed an acute coronary syndrome when treated with nivolumab as second-line therapy for metastatic pulmonary adenocarcinoma. A review of the literature, the French pharmacovigilance registry, and the World Health Organization pharmacovigilance database led to the identification of four cases of patients with coronary manifestations attributable to anti-PD1 immunotherapy (with no reported cases of patients undergoing anti-PD-L1 immunotherapy), which we describe herein. The potential mechanisms causing adverse coronary reactions to this type of therapy, which is used to treat lung cancer as well as other solid and hematological neoplastic diseases, are also discussed.

Indexed as

AgedAntibodies, Monoclonal, HumanizedB7-H1 AntigenCardiotoxicityFemaleHumansImmunotherapyMaleMiddle AgedNivolumabProgrammed Cell Death 1 ReceptorRegistriesAntibodies, Monoclonal, HumanizedB7-H1 AntigenCD274 protein, humanNivolumabPDCD1 protein, humanpembrolizumabProgrammed Cell Death 1 Receptor

Identifiers

PMID30006825
OpenAlexW2883638671

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.