Evidence map›Paper›PMID 33205034›Full record

ReviewJHEP reports : innovation in hepatology2020

Liver toxicity as a limiting factor to the increasing use of immune checkpoint inhibitors.

Eleonora De Martin, Jean-Marie Michot, Olivier Rosmorduc, Catherine Guettier, Didier Samuel

Registry-linked trialOpen access · goldAbstract readReview
In one paragraph

Review in JHEP reports : innovation in hepatology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT06470997 (Specific Biomarkers of Immune-mediated Hepatitis Secondary to Immune Checkpoint), which is not on this map. Cited by 100 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
100citing papers in PubMed, 1 pooled it
7.7field-weighted citation impact, top 2% 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.

NCT06470997 recruitingnot on this mapstarted 2024, after this paper: background citation

Specific Biomarkers of Immune-mediated Hepatitis Secondary to Immune Checkpoint

TypeobservationalSponsorUniversity Hospital, MontpellierRan2024 to 2027Enrolled60ConditionsImmune-mediated HepatitisArmsBlood sample collection, Liver biopsy
3 · Its place in the literature

Who cites it

100 citing papers in PubMed, 1 synthesis or guideline pooled it, 173 citations in OpenAlex.

  1. Anti-PD-1/L1 antibody plus anti-VEGF antibodyExploration of targeted anti-tumor therapy · 2024
    Pooled it
  2. Trial
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. Article
  14. Review
  15. Article
  16. Article
  17. Article
  18. Article
  19. Review
  20. Review

40 more citing papers are in PubMed but not listed here.

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

5 authors at 4 institutions in 1 country.

Eleonora De MartinAP-HP Hôpital Paul-Brousse, Centre Hépato-Biliaire, INSERM Unit 1193, Univ Paris-Sud, Université Paris-Saclay, FHU Hépatinov, Villejuif, F-94800, France.
Jean-Marie MichotDépartement d'innovation thérapeutique et d'Essais Précoces (DITEP), Institut Gustave-Roussy, Université Paris Saclay, Villejuif, France.
Olivier RosmorducAP-HP Hôpital Paul-Brousse, Centre Hépato-Biliaire, INSERM Unit 1193, Univ Paris-Sud, Université Paris-Saclay, FHU Hépatinov, Villejuif, F-94800, France.
Catherine GuettierAP-HP Hôpital Bicêtre, Laboratoire Anatomie Pathologique, Le Kremlin-Bicêtre, France, Univ Paris-Sud, UMR-S 1193, Université Paris-Saclay, France.
Didier SamuelAP-HP Hôpital Paul-Brousse, Centre Hépato-Biliaire, INSERM Unit 1193, Univ Paris-Sud, Université Paris-Saclay, FHU Hépatinov, Villejuif, F-94800, France.
Inserm · FRInstitut Gustave Roussy · FRSorbonne Université · FRUniversité Paris-Saclay · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Immune checkpoint inhibitors (ICIs) improve clinical outcomes in patients suffering from different types of cancer. Liver toxicity is one of the immune-related adverse events associated with immunotherapy; although not common, its management is challenging as it is extremely heterogeneous in terms of presentation and severity. Differences in the development and evolution of ICI-related toxicity in healthy or cirrhotic livers have not yet been elucidated. Assessing causality is key to diagnosing ICI-induced liver toxicity; liver biopsies can assist not only in the differential diagnosis but also in assessing the severity of histological liver damage. The current classification of severity overestimates the grade of liver injury and needs to be revised to reflect the views of hepatologists. Spontaneous improvements in ICI-related liver toxicity have been reported, so corticosteroid therapy should probably be individualised not systematic. The reintroduction of ICIs in a patient with previous immune-mediated hepatitis may be possible, but the risk/benefit ratio should be considered, as the risk factors for hepatitis recurrence are currently unclear. The management of these patients, requiring a balance between efficacy, toxicity and specific treatments, necessitates multidisciplinary collaboration. The incidence of immune-related liver toxicity will continue to rise based on the increasing use of ICIs for most cancers, mandating improved understanding and management of this complication.

Indexed as

AIH, autoimmune hepatitisALP, alkaline phosphataseALT, alanine aminotransferaseAMA, anti-mitochondrial antibodiesANA, anti-nuclear antibodiesanti-LC1, anti-liver cytosol type-1 antibodiesanti-LKM, anti-liver-kidney microsomal antibodiesanti-SLA, anti-soluble liver antigen antibodiesASMA, anti-smooth muscles antibodiesAST, aspartate aminotransferaseCorticosteroid therapyCTLA-4, cytotoxic T lymphocyte-associated protein 4DCR, disease control rateDILI, drug-induced liver injuryGGT, gamma-glutamyltransferaseHCC, hepatocellular carcinomaICI, immune checkpoint inhibitorImmune-mediated hepatitisImmunotherapyINR, international normalised ratioirAE, immune-related adverse eventLiver biopsyMMF, mycophenolate mofetilORR, objective response rateOS, overall survivalPD-1, programmed cell death 1PD-L1-2, programmed cell death ligands 1-2PFS, progression-free survivalTKI, tyrosine kinase inhibitortrAE, treatment-related adverse eventUDCA, ursodeoxycholic acidULN, upper limit of normal

Identifiers

PMID33205034
PMCPMC7648167
OpenAlexW3048739245

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.