Evidence map›Paper›PMID 39911399›Full record

ArticleFrontiers in immunology2025

PDL1 inhibitors may be associated with a lower risk of allograft rejection than PD1 and CTLA4 inhibitors: analysis of the WHO pharmacovigilance database.

Alexandre O Gérard, Diane Merino, Jonathan Benzaquen, Alexandre Destere, Delphine Borchiellini, Clément Gosset, Fanny Rocher, Marine Andreani, Charles-Hugo Marquette, Henri Montaudié and 2 more

Abstract read
In one paragraph

Article in Frontiers in immunology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Review
  2. Article
  3. 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

12 authors.

Alexandre O GérardDepartment of Nephrology-Dialysis-Transplantation, Université Côte d'Azur, University Hospital Centre of Nice, Nice, France.
Diane MerinoDepartment of Clinical Pharmacology, Université Côte d'Azur, University Hospital Centre of Nice, Nice, France.
Jonathan BenzaquenMolecular and Cellular Pharmacology Q6 Institute (IPMC), UMR 7275, CNRS, Université Côte d'Azur, Nice, France.
Alexandre DestereDepartment of Clinical Pharmacology, Université Côte d'Azur, University Hospital Centre of Nice, Nice, France.
Delphine BorchielliniDepartment of Clinical Research and Innovation, Department of Medical Oncology, Centre Antoine Lacassagne, Nice, France.
Clément GossetDepartment of Nephrology-Dialysis-Transplantation, Université Côte d'Azur, University Hospital Centre of Nice, Nice, France.
Fanny RocherDepartment of Clinical Pharmacology, Université Côte d'Azur, University Hospital Centre of Nice, Nice, France.
Marine AndreaniDepartment of Nephrology-Dialysis-Transplantation, Université Côte d'Azur, University Hospital Centre of Nice, Nice, France.
Charles-Hugo MarquetteMolecular and Cellular Pharmacology Q6 Institute (IPMC), UMR 7275, CNRS, Université Côte d'Azur, Nice, France.
Henri MontaudiéDepartment of Dermatology, Université Côte d'Azur, University Hospital Centre of Nice, Nice, France.
Milou-Daniel Drici *Department of Clinical Pharmacology, Université Côte d'Azur, University Hospital Centre of Nice, Nice, France.
Antoine Sicard *Department of Nephrology-Dialysis-Transplantation, Université Côte d'Azur, University Hospital Centre of Nice, Nice, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Transplant recipients face increased cancer mortality due to immunosuppressive treatments. Immune checkpoint inhibitors (ICI) have improved survival rates, but data on the use of these agents in transplant recipients is scarce. ICI may trigger allograft rejection, but the absolute risk of AR between the different ICI classes remains to be defined. Methods: VigiBase Results: We gathered 159 AR involving an ICI, especially nivolumab (73, 45.9%), mostly affecting kidneys (87, 54.7%). Median time to onset: 28 days. Fatal outcome: 36 reports (22.6%). ICI were significantly associated with AR: IC=1.7 [1.4;1.9]. Specifically, PD1 inhibitors yielded an IC of 2.0 [1.7;2.2] (152 reports observed compared to 38 expected). By contrast, the IC of PDL1 inhibitors was negative: -2.6 [-6.4;-1.0] (1 observed, 9 expected). The comparative ROR of PD1 compared to PDL1 inhibitors was 33.7 [4.7;240.9] (p=0.0005). Conclusions: We confirm the association between ICI treatment and AR. Notably, PDL1 inhibitors showed surprisingly low AR reports compared to CTLA4 and PD1 inhibitors. Further prospective studies are warranted to confirm whether PDL1 inhibitors indeed reduce AR risk compared to other ICI.

Indexed as

B7-H1 AntigenCTLA-4 AntigenGraft RejectionImmune Checkpoint InhibitorsProgrammed Cell Death 1 ReceptorAdultAgedDatabases, FactualFemaleHumansMaleMiddle AgedPharmacovigilanceWorld Health OrganizationYoung AdultB7-H1 AntigenCD274 protein, humanCTLA-4 AntigenCTLA4 protein, humanImmune Checkpoint InhibitorsPDCD1 protein, humanProgrammed Cell Death 1 Receptorallograft rejectionimmune checkpoint inhibitorsoncologypharmacovigilancetransplantation

Identifiers

PMID39911399
PMCPMC11794220

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.