Evidence map›Paper›PMID 42435281›Full record

ReviewInternational journal of clinical oncology2026

The immunological paradox: immune checkpoint inhibitors in liver transplantation.

Takashi Ito, Shinya Okumura, Katsunori Sakamoto, Etsuro Hatano

Abstract readReview
In one paragraph

Review in International journal of clinical oncology, 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

4 authors.

Takashi ItoDepartment of Surgery, Graduate School of Medicine, Kyoto University, 54 Kawahara-Cho, Shogoin, Sakyo-Ku, Kyoto, 606-8507, Japan. itotaka@kuhp.kyoto-u.ac.jp.ORCID http://orcid.org/0000-0002-5892-8317
Shinya OkumuraDepartment of Surgery, Graduate School of Medicine, Kyoto University, 54 Kawahara-Cho, Shogoin, Sakyo-Ku, Kyoto, 606-8507, Japan.
Katsunori SakamotoDepartment of Surgery, Graduate School of Medicine, Kyoto University, 54 Kawahara-Cho, Shogoin, Sakyo-Ku, Kyoto, 606-8507, Japan.
Etsuro HatanoDepartment of Surgery, Graduate School of Medicine, Kyoto University, 54 Kawahara-Cho, Shogoin, Sakyo-Ku, Kyoto, 606-8507, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The incorporation of immune checkpoint inhibitors (ICIs) into the treatment repertoire for hepatocellular carcinoma (HCC) and advanced biliary tract cancers has significantly transformed the field of oncology, offering remarkable survival advantages. However, the interaction of these powerful immunomodulators with liver transplantation (LT), the ultimate curative intervention for end-stage liver disease, presents a complex immunological paradox. While LT depends on the induction and maintenance of immune tolerance to suppress alloimmune responses and prevent allograft rejection, ICIs operate by disrupting these tolerance mechanisms to enhance host antitumor immunity. This comprehensive review synthesizes the latest evidence from 2024 and 2025, incorporating key findings from the VITALITY study, international washout cohorts, and meta-analyses of individual patient data. The historical "Liver Tolerance Effect," the mechanistic role of the PD-1/PD-L1 axis as a crucial protector of hepatic integrity, and the severe phenomenon of ICI-induced fatal hepatic necrosis are critically examined in this review. Furthermore, the emerging utility of precision predictive biomarkers, including immune-related adverse events (irAEs), the Eplet Risk Score, and intragraft PD-L1 expression as tissue-based predictors of post-transplant ICI-induced rejection, was rigorously analyzed to stratify rejection risk. By examining the pharmacodynamic conflict between systemic tumor eradication and localized graft preservation, this report provides a pragmatic, evidence-based framework for candidate selection, optimal washout timing, and post-transplant management, ultimately culminating in a critical appraisal of the ethical imperatives surrounding living donor liver transplantation.

Indexed as

Carcinoma, HepatocellularGraft RejectionImmune Checkpoint InhibitorsLiver NeoplasmsLiver TransplantationB7-H1 AntigenHumansB7-H1 AntigenImmune Checkpoint InhibitorsHepatocellular carcinomaImmune checkpoint inhibitorLiver transplantationPerihilar cholangiocarcinomaT cell mediated rejection

Identifiers

PMID42435281
PMCPMC13401545

What OpenQuestion holds

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LicenceCC BY
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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.