Evidence map›Paper›PMID 41640611›Full record

ReviewWorld journal of gastroenterology2026

Post-immunotherapy second-line strategies for hepatocellular carcinoma: State of the art and ongoing trials.

Sara Ascari, Rusi Chen, Andrea De Sinno, Bernardo Stefanini, Matteo Cescon, Matteo Serenari, Cristina Mosconi, Francesco Tovoli

Abstract readReview
In one paragraph

Review in World journal of gastroenterology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Review
  2. Review
  3. Review
  4. 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

8 authors.

Sara AscariDepartment of Medical and Surgical Sciences, University of Bologna, Bologna 40138, Emilia-Romagna, Italy.
Rusi ChenDepartment of Medical and Surgical Sciences, University of Bologna, Bologna 40138, Emilia-Romagna, Italy.
Andrea De SinnoDepartment of Medical and Surgical Sciences, University of Bologna, Bologna 40138, Emilia-Romagna, Italy.
Bernardo StefaniniDepartment of Medical and Surgical Sciences, University of Bologna, Bologna 40138, Emilia-Romagna, Italy.
Matteo CesconDepartment of Medical and Surgical Sciences, University of Bologna, Bologna 40138, Emilia-Romagna, Italy.
Matteo SerenariDepartment of Medical and Surgical Sciences, University of Bologna, Bologna 40138, Emilia-Romagna, Italy.
Cristina MosconiDepartment of Medical and Surgical Sciences, University of Bologna, Bologna 40138, Emilia-Romagna, Italy.
Francesco TovoliDepartment of Medical and Surgical Sciences, University of Bologna, Bologna 40138, Emilia-Romagna, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The treatment landscape of hepatocellular carcinoma (HCC) has significantly evolved following the introduction of immune checkpoint inhibitors (ICIs), which are now the standard of care in first-line systemic therapy. However, as more patients experience progression after ICI-based combinations, the optimal second-line treatment strategy remains undefined. Currently approved agents, such as regorafenib, cabozantinib, and ramucirumab, have not been specifically tested in the post-ICI setting, and their efficacy in this context remains uncertain. This review provides a comprehensive and critical analysis of systemic second-line treatment strategies in patients with unresectable HCC after progression to frontline immunotherapy. We summarize the available evidence from early-phase studies and retrospective series and describe the rationale, efficacy signals, and development status of ongoing clinical trials. Therapeutic approaches include tyrosine kinase inhibitors, novel ICI-based combinations, bispecific antibodies, T-cell therapies (chimeric antigen receptor-T and T-cell receptor-T), and other emerging strategies such as liver-targeted prodrugs and microbiota modulation. While current data are still limited, several trials are ongoing and reflect compelling biological hypotheses. Their diversity highlights both the complexity and the opportunity of this therapeutic space. Future research should focus on identifying predictive biomarkers, optimizing safety, and developing individualized sequencing strategies to enhance outcomes in this rapidly expanding patient population.

Indexed as

Antineoplastic Combined Chemotherapy ProtocolsCarcinoma, HepatocellularImmune Checkpoint InhibitorsImmunotherapyLiver NeoplasmsAntibodies, BispecificClinical Trials as TopicDisease ProgressionHumansProtein Kinase InhibitorsTreatment OutcomeAntibodies, BispecificImmune Checkpoint InhibitorsProtein Kinase InhibitorsAdoptive T-cell therapyBispecific antibodiesChimeric antigen receptor-T cellsClinical trialsHepatocellular carcinomaImmune checkpoint inhibitorsPost-immunotherapy progressionSecond-line therapyTreatment sequencingTyrosine kinase inhibitors

Identifiers

PMID41640611
PMCPMC12865376

What OpenQuestion holds

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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.