Evidence map›Paper›PMID 41142624›Full record

ArticleFrontiers in oncology2025

Treatment experience in managing severe immune-mediated hepatotoxicity induced by immune checkpoint inhibitors.

Ruijie Cao, Shasha Zhang, Jingjing Zhang, Yufei Zhao, Xiaoyun Zhang, Zhanjun Guo

Abstract read
In one paragraph

Article in Frontiers in oncology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

6 authors.

Ruijie CaoDepartment of Immunology and Rheumatology, The Fourth Hospital of Hebei Medical University, Shijiazhuang, China.
Shasha ZhangDepartment of Immunology and Rheumatology, The Fourth Hospital of Hebei Medical University, Shijiazhuang, China.
Jingjing ZhangDepartment of Immunology and Rheumatology, The Fourth Hospital of Hebei Medical University, Shijiazhuang, China.
Yufei ZhaoDepartment of Immunology and Rheumatology, The Fourth Hospital of Hebei Medical University, Shijiazhuang, China.
Xiaoyun ZhangDepartment of Immunology and Rheumatology, The Fourth Hospital of Hebei Medical University, Shijiazhuang, China.
Zhanjun GuoDepartment of Immunology and Rheumatology, The Fourth Hospital of Hebei Medical University, Shijiazhuang, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Although multiple guidelines for managing severe immune-mediated hepatotoxicity (IMH) induced by immune checkpoint inhibitors (ICIs) were recommended, real-world research data regarding its clinical progression, treatment modalities, and outcomes remain scarce. Methods: This study was a retrospective, single-center investigation conducted at the Fourth Hospital of Hebei Medical University. A total of 379 patients with complete clinical records were enrolled in the Department of Immunology and Rheumatology at the Fourth Hospital of Hebei Medical University from January 2021 to July 2024. Binary logistic regression analysis was employed to identify potential risk factors associated with the development of severe IMH or infection during treatment. Receiver operating characteristic (ROC) curve analysis was further applied to determine the optimal cutoff values for the identified risk factors. Results: A total of 32 severe IMH patients were analyzed for risk factor association; the Eastern Cooperative Oncology Group performance status (ECOG PS) (p = 0.001) and oral traditional Chinese medicine (TCM) (p < 0.001) were independently associated with the incidence of severe IMH. Based on our experience with these 32 patients, a road map was proposed for the management of severe IMH patients: conventional applications of daily methylprednisolone sodium succinate with dose adjustment for 11 days, a liver biopsy to exclude vanishing bile duct syndrome for steroid-resistant patients, and subsequent plasma exchange (PE). Furthermore, cumulative steroid use was identified as an independent risk factor for concurrent infection with a cutoff value of 1,656 mg (p = 0.024) in severe IMH patients. Conclusion: We investigated the risk factor of severe IMH and provided a feasible treatment roadmap for severe IMH.

Indexed as

immune checkpoint inhibitorsimmune-mediated hepatotoxicityimmune-related adverse eventsplasma exchangesteroid

Identifiers

PMID41142624
PMCPMC12549241

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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.