Evidence map›Paper›PMID 41048450›Full record

ReviewJournal of clinical and experimental hepatology

Evolving Landscape of Systemic Therapy for Hepatocellular Carcinoma in 2025.

Karan Kumar, Vivek A Saraswat

Abstract readReview
In one paragraph

Review in Journal of clinical and experimental hepatology. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Article
  2. Review
  3. Review
  4. Review
  5. Article
  6. 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

2 authors.

Karan KumarDepartment of Hepatology and Liver Transplantation, Mahatma Gandhi University of Medical Sciences and Technology, Jaipur, India.
Vivek A SaraswatDepartment of Hepatology and Liver Transplantation, Mahatma Gandhi University of Medical Sciences and Technology, Jaipur, India.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hepatocellular carcinoma (HCC), the sixth most common malignant tumor, accounts for approximately 90% of liver cancers. HCC is frequently diagnosed at an advanced stage, where systemic therapy becomes the primary treatment option. As understanding about the molecular signaling pathways within tumors and the tumor microenvironment have evolved, treatment option for advanced HCC has also become more innovative. Current therapies target cellular pathways, including tyrosine kinase inhibitors (TKIs) like lenvatinib, sorafenib, regorafenib, and cabozantinib, which disrupt signals crucial for tumor growth and survival; VEGF (vascular endothelial growth factor) inhibitors that block tumor blood vessel formation; and immunotherapy agents such as atezolizumab-bevacizumab, tremelimumab, and durvalumab, which stimulate the immune system to attack cancer cells. Both targeted therapies and immunotherapies, used alone or in combination, have demonstrated efficacy in clinical trials. The treatment landscape for HCC is rapidly evolving, driven by recent landmark trial results exploring innovative strategies and drug combinations. This review examines these exciting advancements in systemic therapy, highlighting their transformative potential and the promise of more effective, personalized treatment regimens. These developments offer hope for improved patient outcomes and a deeper understanding of this complex disease.

Indexed as

advanced HCCimmunotherapytargeted therapy

Identifiers

PMID41048450
PMCPMC12490691

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.