Evidence map›Paper›PMID 42882810›Full record

ReviewCancers2026

The Rationale for Tissue Biopsy in the Era of Precision Hepatocellular Carcinoma Management.

Ioanna-Maria Grypari, Dina G Tiniakos, Maria Kalafateli, Eleni Theocharidou

Abstract readReview
In one paragraph

Review in Cancers, 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.

Ioanna-Maria GrypariPathology Department, Faculty of Medicine, School of Health Sciences, University of Ioannina, 45500 Ioannina, Greece.ORCID 0000-0001-6042-6554
Dina G TiniakosDepartment of Pathology, Aretaeion Hospital, School of Medicine, National and Kapodistrian University of Athens, 11528 Athens, Greece.
Maria Kalafateli4th Department of Internal Medicine, Hippokration General Hospital, Aristotle University of Thessaloniki, 54124 Thessaloniki, Greece.
Eleni TheocharidouSecond Department of Internal Medicine, Hippokration General Hospital, Aristotle University of Thessaloniki, 54124 Thessaloniki, Greece.ORCID 0000-0001-8136-3927

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hepatocellular carcinoma (HCC) is the most common liver cancer and usually develops on a background of cirrhotic liver. Early and accurate diagnosis enables potentially curative interventions. HCC surveillance, usually offered to patients at risk for HCC, such as those with cirrhosis, chronic hepatitis B infection, and previous diagnosis of HCC, is associated with earlier detection and improved survival. In these patients, the diagnosis can be established non-invasively without histological confirmation when the imaging-based LI-RADS criteria are met. Tissue biopsy is mandatory for establishing diagnosis in patients without cirrhosis or other risk factors for HCC, differentiating HCC from other malignant and non-malignant entities, especially when imaging features are not conclusive. In this review, we discuss the evolving role of tissue biopsy beyond establishing the diagnosis, in providing important prognostic information and enabling precise histopathological classification. Features such as poor differentiation, microvascular invasion, and a pattern of vessels encapsulating tumor clusters are linked to worse prognosis. HCC is characterized by heterogeneity, with different histological subtypes associated with distinct clinical and radiological features and distinct biology. Emerging data from molecular profiling and immune-microenvironment studies enable further classification into proliferative versus non-proliferative molecular subgroups and inflamed versus non-inflamed immune subtypes. This more refined characterization of HCC carries important implications not only for prognostication but also for predicting response to immunotherapy. In the future, the combination of imaging features that correlate with molecular signatures, novel serum biomarkers, and liquid biopsy may provide less invasive tools for early detection, risk stratification, and guide personalized therapeutic strategies.

Indexed as

hepatocellular carcinomahistologic subtypesLI-RADSmolecular subtypespredictionprognosissurveillancetissue biopsy

Identifiers

PMID42882810
PMCPMC13664514

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.