Evidence map›Paper›PMID 32865910›Full record

ReviewCritical reviews in oncogenesis2020

Targeted Molecular Therapeutic Options for Hepatocellular Carcinoma.

Swathi Sridhar, Ishna Sharma, Umesh T Sankpal, Bassam Ghabach, Kalyani Narra, Latha Neerukonda, Riyaz Basha

Open access · greenAbstract readReview
In one paragraph

Review in Critical reviews in oncogenesis, 2020. 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
0.1field-weighted citation impact, top 53% 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.

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, 5 citations in OpenAlex.

  1. Review
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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

7 authors at 3 institutions in 1 country.

Swathi SridharTexas College of Osteopathic Medicine, University of North Texas Health Science Center at Fort Worth, Fort Worth, Texas.
Ishna SharmaTexas College of Osteopathic Medicine, University of North Texas Health Science Center at Fort Worth, Fort Worth, Texas.
Umesh T SankpalTexas College of Osteopathic Medicine, University of North Texas Health Science Center, Fort Worth, Texas 76107.
Bassam GhabachJPS Oncology & Infusion Center, Fort Worth, Texas.
Kalyani NarraJPS Oncology & Infusion Center, Fort Worth, Texas.
Latha NeerukondaJPS Oncology and Infusion Center, Fort Worth, Texas.
Riyaz BashaGraduate School of Biomedical Sciences, The University of North Texas Health Science Center, Fort Worth, Texas; Department of Pediatrics and Women's Health, Texas College of Osteopathic Medicine, The University of North Texas Health Science Center, Fort Worth, Texas.
Texas College · USUniversity of North Texas · USUniversity of North Texas Health Science Center · US

Funding

Texas Center for Minority Health, Education, Research and OutreachU54MD006882 · NIMHD · UNIVERSITY OF NORTH TEXAS HLTH SCI CTR · PI JONES, HARLAN PIERRE, VISHWANATHA, JAMBOOR K. · 2017 to 2022
$6.0M
2/2 Pilot Project 2: Langston University-UNTHSC Partnership for Cancer Research and EducationP20CA233355 · NCI · UNIVERSITY OF NORTH TEXAS HLTH SCI CTR · PI BASHA, RIYAZ · 2018 to 2021
$1.0M
NCI NIH HHS P20 CA233355NIMHD NIH HHS U54 MD006882
6 · The paper itself

Abstract

Liver cancer is the 6th leading cause of cancer related deaths in the US even though it ranks 14th in incidence. More men are diagnosed with liver cancer than women, and the number of projected deaths among men (20,020) is almost double that among women (10,140) in the US. Infections like hepatitis and metabolic conditions like obesity are believed to be major risk factors for the onset of liver cancer. Hepatocellular carcinoma (HCC), the most common type of liver cancer, accounts for 75% of all cases. Chemotherapy has not been effective in treating HCC. Targeted therapies are being used in advanced HCC patients due to a better survival and less side effects when compared to traditional chemotherapy. Therapeutic agents targeting the regulators of growth factor signaling pathways and the mediators of downstream signaling-for example, inhibitors of the tyrosine kinase receptor-are used as targeted molecular therapies. Kinase inhibitors that modulate growth signals, such as sorafenib and lenvatinib, are commonly employed in targeted molecular therapy for HCC patients. This review covers these agents, highlighting modes of action and providing details on clinical trials.

Indexed as

Carcinoma, HepatocellularClinical Trials as TopicHumansLiver NeoplasmsMolecular Targeted TherapyPhenylurea CompoundsQuinolinesSignal TransductionSorafeniblenvatinibPhenylurea CompoundsQuinolinesSorafenib

Identifiers

PMID32865910
PMCPMC11079775
OpenAlexW3036421504

What OpenQuestion holds

Textmetadata
LicenceTDM
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.