Evidence map›Paper›PMID 41659771›Full record

ArticleJHEP reports : innovation in hepatology2026

Plasma exchange as potential treatment of severe immune checkpoint inhibitor-induced hepatitis.

Lucy Meunier, Clement Monet, Antonio Saviano, Marwin Farrugia, François Villeret, Fanny Lebossé, Marion Khaldi, Olivier Moranne, Christine Chambon, Philippe Ichai and 8 more

Abstract read
In one paragraph

Article in JHEP reports : innovation in hepatology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

18 authors.

Lucy MeunierLiver Unit, Saint-Eloi Hospital, INSERM 1183, Montpellier School of Medicine, Montpellier, France.
Clement MonetDepartment of Anesthesia and Intensive Care unit, Regional University Hospital of Montpellier, St-Eloi Hospital, University of Montpellier, Montpellier, CEDEX 5, France; PhyMedExp, INSERM U1046, CNRS UMR, 9214, Montpellier, France.
Antonio SavianoGastroenterology and Hepatology Service, Strasbourg University Hospitals, Strasbourg, France.
Marwin FarrugiaArchet 2 University Hospital, Inserm U1065 Team 8, Université Côte d'Azur, Nice, France.
François VilleretDepartment of Hepatology, Hospices Civils de Lyon; Université Claude Bernard Lyon 1; INSERM Unit 1350 PathLiv; Lyon Hepatology Institute, IHU EVEREST; Lyon, France.
Fanny LebosséDepartment of Hepatology, Hospices Civils de Lyon; Université Claude Bernard Lyon 1; INSERM Unit 1350 PathLiv; Lyon Hepatology Institute, IHU EVEREST; Lyon, France.
Marion KhaldiCHU Nantes, Nantes Université, Service Hépato-Gastroentérologie, IMAD, Nantes, France.
Olivier MoranneService de Nephrologie-Dialyse-Apherese, Hôpital Universitaire Carémeau Nimes, IDESP Université de Montpellier, France.
Christine ChambonDepartment of Hepatology, Hôpital Edouard Herriot, Hospices Civils de Lyon, University of Lyon, 69003, Lyon, France.
Philippe IchaiAP-HP Hôpital Paul-Brousse, Centre Hépato-Biliaire, INSERM Unit 1193, Université Paris-Saclay, FHU Hepatinov, Villejuif, F-94800, France.
Astrid Laurent-BellueHôpital Kremlin Bicêtre, Anatomie & Cytologie Pathologiques, Le Kremlin Bicetre, France.
Ariane LaparraInterdisciplinary Department for the Organization of Patient Pathways-DIOPP, Gustave Roussy, Villejuif, France.
Rodolphe AntyArchet 2 University Hospital, Inserm U1065 Team 8, Université Côte d'Azur, Nice, France.
Simona TriponGastroenterology and Hepatology Service, Strasbourg University Hospitals, Strasbourg, France.
Mialy RandrianarisoaGastroenterology and Hepatology Service, Strasbourg University Hospitals, Strasbourg, France.
Alexandre MariaInternal Medicine and Multi-Organic Diseases Department, Hôpital Saint Éloi, CHU Montpellier, IRMB, University of Montpellier, INSERM, Montpellier, France.
Lina HountondjiLiver Unit, Saint-Eloi Hospital, INSERM 1183, Montpellier School of Medicine, Montpellier, France.
Eleonora De MartinAP-HP Hôpital Paul-Brousse, Centre Hépato-Biliaire, INSERM Unit 1193, Université Paris-Saclay, FHU Hepatinov, Villejuif, F-94800, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background & Aims: Immune checkpoint inhibitors (ICIs) improve cancer survival but can cause severe immune-related hepatitis. Standard therapy with corticosteroids and second-line agents such as mycophenolate mofetil fails in some cases. Therapeutic plasma exchange (TPE) has been suggested as rescue therapy, but supporting evidence is limited. Methods: We retrospectively analyzed French multicenter data (March 2021-April 2025) on patients with grade 4 ICI-induced hepatitis refractory to corticosteroids ± other immunosuppressants who underwent TPE. Results: Thirteen patients (median age 63 years; 54% male) were included. Eleven had acute hepatitis, including seven with acute liver injury, and two had steroid-refractory cholestatic hepatitis. TPE was initiated a median of 28 days after hepatitis onset (median MELD score 21) and administered in 2-8 sessions. Liver function improved in eight patients (61.5%), allowing resumption of anticancer therapy without ICI rechallenge in five. Three patients with cirrhosis and hepatocellular carcinoma died of liver failure, and three died from other causes. TPE-related adverse events were mild to moderate. Conclusion: TPE is feasible, safe, and may be effective for severe steroid- and immunosuppressant-refractory ICI-induced hepatitis. Early initiation could improve outcomes; prospective studies are needed to clarify optimal timing and patient selection. Impact and implications: Severe immune checkpoint inhibitor-induced hepatitis represents a rare but life-threatening complication for which therapeutic options are limited once corticosteroids and immunosuppressants fail. Our study provides the first multicenter evidence suggesting that therapeutic plasma exchange (TPE) is a feasible and safe approach that may improve hepatic outcomes in this setting. These findings are particularly relevant for oncologists, hepatologists, and intensivists facing refractory immune checkpoint inhibitor-induced liver injury, as TPE could offer a bridge to recovery when liver transplantation is not feasible. Early consideration of TPE, alongside careful patient selection, could optimize outcomes, although larger prospective studies are required to confirm efficacy and define the best timing and indications.

Indexed as

Acute liver failureCheckpoint inhibitor-induced liver injuryTherapeutic plasma exchange

Identifiers

PMID41659771
PMCPMC12873720

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