Evidence map›Paper›PMID 40755508›Full record

ArticleTransplantation direct2025

Immune Checkpoint Inhibitors in Kidney Transplant Recipients: A French Multicenter Retrospective Cohort Study.

Tristan Legris, Marion Sallée, Xavier Charmetant, Olivier Thaunat, Marie Matignon, Nizar Joher, Vincent Pernin, Antoine Sicard, Hannah Kaminski, Lionel Couzi and 1 more

Abstract read
In one paragraph

Article in Transplantation direct, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Article
  2. Ten tips for kidney biopsy in cancer patients.Clinical kidney journal · 2026
    Review
  3. Article
  4. Article
  5. Review
  6. 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

11 authors.

Tristan LegrisDepartment of Nephrology and Kidney Transplantation, APHM, Conception University Hospital, Marseille, France.
Marion SalléeDepartment of Nephrology and Kidney Transplantation, APHM, Conception University Hospital, Marseille, France.
Xavier CharmetantDepartment of Transplantation, Nephrology, and Clinical Immunology, Edouard Herriot Hospital, HCL, Lyon, France.
Olivier ThaunatDepartment of Transplantation, Nephrology, and Clinical Immunology, Edouard Herriot Hospital, HCL, Lyon, France.
Marie MatignonDepartment of Nephrology and Transplantation, APHP, Henri Mondor University Hospital, Créteil, France.
Nizar JoherDepartment of Nephrology and Transplantation, APHP, Henri Mondor University Hospital, Créteil, France.
Vincent PerninNephrology, Dialysis and Transplantation Department, Lapeyronie University Hospital, Montpellier, France.
Antoine SicardDepartment of Nephrology, Dialysis and Transplantation, Pasteur University Hospital, Nice, France.
Hannah KaminskiDepartment of Nephrology, Transplantation, Dialysis and Apheresis, Bordeaux University Hospital, Bordeaux, France.
Lionel CouziDepartment of Nephrology, Transplantation, Dialysis and Apheresis, Bordeaux University Hospital, Bordeaux, France.
Valérie MoalDepartment of Nephrology and Kidney Transplantation, APHM, Conception University Hospital, Marseille, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Kidney transplant recipients (KTRs) are at elevated risk of malignancy. Data on the safety and efficacy of immune checkpoint inhibitors (ICIs) in this population remain limited. We aimed to reassess the benefit-risk profile of ICI therapy in KTRs using a multicenter cohort, in the recent era. Methods: We conducted a retrospective cohort study of all KTRs treated with ICIs for advanced or metastatic cancer, across 6 transplant centers. We evaluated cancer response, acute rejection (AR) incidence, graft survival, and patient survival. Results: From 2015 to 2024, 34 KTRs were analyzed. The most common cancers were cutaneous (56%) and non-small cell lung cancer (32%). Pembrolizumab was the most used ICI (53%). The objective response rate was 38%, with a median progression-free survival of 5.5 mo and an overall survival of 10.7 mo. Biopsy-proven AR occurred in 26.5% of patients, at a median time of 52 d after ICI start. All rejection episodes involved T cells, and one-third showed additional humoral features. No clinical predictors of AR were identified. Among all patients, 29% had a favorable outcome (tumor response without ICI-induced graft loss), 12% experienced a tumor response with graft loss, 59% had progression disease without graft loss, and 3% experienced the worst outcome (progression disease with graft loss). Conclusions: Our study suggests that ICI therapy is a viable option for KTRs with poor-prognosis cancers, demonstrating a 38% tumor response rate and a lower incidence of graft loss (15%) compared with previously reported rates. Prospective studies are needed to optimize the use of ICI in KTRs.

Identifiers

PMID40755508
PMCPMC12316348

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Registered trials

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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.