ReviewJournal of gastroenterology and hepatology2026
Systemic Therapy for Advanced Hepatocellular Carcinoma in 2026: Current Standard-of-Care and Emerging Therapeutic Strategies.
Review in Journal of gastroenterology and hepatology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.
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.
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.
Who cites it
2 citing papers in PubMed.
- Article
- Independent Prognosis Prediction of Hepatocellular Carcinoma Using MicroRNA-Based Single and Combined Biomarkers.Canadian journal of gastroenterology & hepatology · 2026Review
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
3 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Hepatocellular carcinoma (HCC) is the most common type of primary liver cancer, accounting for up to 80% of all cases. Most patients present at an advanced stage and are unsuitable for curative treatments. In the past 5 years, immunotherapy combination has superseded tyrosine kinase inhibitors (TKI) as the standard first-line therapy for advanced HCC. These therapies include the combination of anti-PD-(L)1 with an anti-CTLA-4 or partner with anti-VEGF; these agents offer unprecedented high rates of response and survival. Unfortunately, only about 20%-30% of patients respond to first-line immunotherapy combination, and about 50% of them would develop disease progression at 6 months. In patients with progression on immunotherapy, recent prospective studies support the efficacy and safety of multiple TKIs. To further improve the efficacy of systemic therapies, novel therapeutic strategies are actively being investigated, such as with the addition of a third immune checkpoint inhibitor. Furthermore, there is increasing interest to incorporate locoregional therapies in patients with advanced disease. Three Phase 3 randomized studies (EMERALD-1, LEAP-012, and TALENTACE) have recently demonstrated survival benefits with the combination of trans-arterial chemoembolization (TACE) and immunotherapy, over TACE alone. The higher response rates brought by combining locoregional therapies and systemic therapies have enabled the possibility of downstaging and conversion. In addition, cellular therapy has shown promise in early phase studies, demonstrating potential to expand the use of immunotherapy in HCC beyond immune checkpoint inhibitors. In this review, we provide an overview of the current treatment landscape and emerging therapeutic strategies for advanced HCC.
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What OpenQuestion holds
Registered trials
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.