Evidence map›Paper›PMID 30061739›Full record

ReviewNature reviews. Clinical oncology2018

Molecular therapies and precision medicine for hepatocellular carcinoma.

Josep M Llovet, Robert Montal, Daniela Sia, Richard S Finn

5 registry-linked trialsOpen access · greenAbstract readReview
In one paragraph

Review in Nature reviews. Clinical oncology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 5 registered trials, which are not on this map. Cited by 1,164 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
1,164citing papers in PubMed, 4 pooled it
101.9field-weighted citation impact, top 1% of its field
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.

NCT04445532 unknown statusnot on this mapstarted 2020, after this paper: background citation

Acquisition of Blood and Tumor Tissue Samples From Patients With Hepatobiliary Tumors

TypeobservationalSponsorPeking Union Medical College HospitalRan2020 to 2025Enrolled450ConditionsHepatocellular Carcinoma, Cholangiocarcinoma, Gallbladder Cancer, Biliary Tract CancerArmsGene expression analysis, Genomic analysis, Protein expression analysis, Proteomic profiling, Polymerase chain reaction
NCT04862949 completednot on this mapstarted 2021, after this paper: background citation

Organ-specific Responses to Atezolizumab Plus Bevacizumab in Patients With Advanced Hepatocellular Carcinoma

TypeobservationalSponsorCHA UniversityRan2021 to 2023Enrolled131ConditionsAdvanced Hepatocellular CarcinomaArmsAtezolizumab plus bevacizumab
NCT05173298 unknown statusnot on this mapstarted 2021, after this paper: background citation

Investigation of Predictive Biomarkers in Patients With Advanced Hepatocellular Carcinoma Treated With Atezolizumab Plus Bevacizumab

TypeobservationalSponsorCHA UniversityRan2021 to 2024Enrolled100ConditionsAdvanced Hepatocellular CarcinomaArmsatezolizumab plus bevacizumab
NCT05197504 completednot on this mapstarted 2021, after this paper: background citation

Biomarker Discovery Through Multiomics Study in Advanced Hepatocellular Carcinoma Patients Who Received Atezolizumab and Bevacizumab Combination Therapy

TypeobservationalSponsorCHA UniversityRan2021 to 2023Enrolled166ConditionsHepatocellular CarcinomaArmsatezolizumab plus bevacizumab
NCT07113418 not yet recruitingnot on this mapstarted 2025, after this paper: background citation

Role of Fibroblast Growth Factor 21(FGF21) in Breast Cancer

Typeobservational_patient_registrySponsorAssiut UniversityRan2025 to 2026Enrolled84ConditionsBreast CancerArmsELISA
3 · Its place in the literature

Who cites it

1,164 citing papers in PubMed, 4 syntheses or guidelines pooled it, 1,979 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Pooled it
  4. Pooled it
  5. Trial
  6. Current patterns of next-generation sequencing implementation in hepatocellular carcinoma in Spain.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2026
    Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Review
  14. Review
  15. Review
  16. Article
  17. Cytotoxic Activity ofInternational journal of molecular sciences · 2026
    Article
  18. Article
  19. A Review of Recent Advances in Chimeric Antigen Receptor (CAR) T-Cell Therapy for Hepatocellular Carcinoma.Medical science monitor : international medical journal of experimental and clinical research · 2026
    Review
  20. Article

1,104 more citing papers are in PubMed but not listed here.

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 at 4 institutions in 2 countries.

Josep M LlovetMount Sinai Liver Cancer Program, Division of Liver Diseases, Tisch Cancer Institute, Icahn School of Medicine at Mount Sinai, New York, NY, USA. Josep.Llovet@mssm.edu.ORCID http://orcid.org/0000-0003-0547-2667
Robert MontalLiver Cancer Translational Lab, Barcelona Clinic Liver Cancer (BCLC) Group, Liver Unit, Hospital Clinic Barcelona, IDIBAPS, University of Barcelona, Barcelona, Spain.
Daniela SiaMount Sinai Liver Cancer Program, Division of Liver Diseases, Tisch Cancer Institute, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Richard S FinnDepartment of Medicine, Division of Hematology/Oncology, Geffen School of Medicine, University of California, Los Angeles (UCLA), Los Angeles, CA, USA.
Hospital Clínic de Barcelona · ESIcahn School of Medicine at Mount Sinai · USUniversitat de Barcelona · ESUniversity of California, Los Angeles · US

Funding

THE TISCH CANCER INSTITUTE - CANCER CENTER SUPPORT GRANTP30CA196521 · NCI · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI Deanna L Benson · 2015 to 2026
$35.4M
NCI NIH HHS P30 CA196521NIH HHS P30 CA196521
6 · The paper itself

Abstract

The global burden of hepatocellular carcinoma (HCC) is increasing and might soon surpass an annual incidence of 1 million cases. Genomic studies have established the landscape of molecular alterations in HCC; however, the most common mutations are not actionable, and only ~25% of tumours harbour potentially targetable drivers. Despite the fact that surveillance programmes lead to early diagnosis in 40-50% of patients, at a point when potentially curative treatments are applicable, almost half of all patients with HCC ultimately receive systemic therapies. Sorafenib was the first systemic therapy approved for patients with advanced-stage HCC, after a landmark study revealed an improvement in median overall survival from 8 to 11 months. New drugs - lenvatinib in the frontline and regorafenib, cabozantinib, and ramucirumab in the second line - have also been demonstrated to improve clinical outcomes, although the median overall survival remains ~1 year; thus, therapeutic breakthroughs are still needed. Immune-checkpoint inhibitors are now being incorporated into the HCC treatment armamentarium and combinations of molecularly targeted therapies with immunotherapies are emerging as tools to boost the immune response. Research on biomarkers of a response or primary resistance to immunotherapies is also advancing. Herein, we summarize the molecular targets and therapies for the management of HCC and discuss the advancements expected in the near future, including biomarker-driven treatments and immunotherapies.

Indexed as

Molecular Targeted TherapyPrecision MedicineAnilidesAntibodies, MonoclonalAntibodies, Monoclonal, HumanizedCarcinoma, HepatocellularHumansImmunotherapyLiver NeoplasmsPhenylurea CompoundsPyridinesQuinolinesRamucirumabSorafenibAnilidesAntibodies, MonoclonalAntibodies, Monoclonal, HumanizedcabozantiniblenvatinibPhenylurea CompoundsPyridinesQuinolinesRamucirumabregorafenibSorafenib

Identifiers

PMID30061739
PMCPMC12452113
OpenAlexW2883204623

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

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.