Evidence map›Paper›PMID 27785449›Full record

ReviewJournal of hepatocellular carcinoma2016

Hepatocellular carcinoma: a review.

Julius Balogh, David Victor, Emad H Asham, Sherilyn Gordon Burroughs, Maha Boktour, Ashish Saharia, Xian Li, R Mark Ghobrial, Howard P Monsour

Abstract readReview
In one paragraph

Review in Journal of hepatocellular carcinoma, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 584 papers, 6 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
584citing papers in PubMed, 6 pooled it
–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

584 citing papers in PubMed, 6 syntheses or guidelines pooled it.

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524 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

9 authors.

Julius BaloghSherrie and Alan Conover Center for Liver Disease and Transplantation; Division of Transplantation, Department of Surgery.
David VictorSherrie and Alan Conover Center for Liver Disease and Transplantation; Department of Gastroenterology and Transplant Hepatology; Department of Medicine, Houston Methodist Hospital, Houston, TX, USA.
Emad H AshamSherrie and Alan Conover Center for Liver Disease and Transplantation; Division of Transplantation, Department of Surgery.
Sherilyn Gordon BurroughsSherrie and Alan Conover Center for Liver Disease and Transplantation; Division of Transplantation, Department of Surgery.
Maha BoktourSherrie and Alan Conover Center for Liver Disease and Transplantation; Division of Transplantation, Department of Surgery.
Ashish SahariaSherrie and Alan Conover Center for Liver Disease and Transplantation; Division of Transplantation, Department of Surgery.
Xian LiSherrie and Alan Conover Center for Liver Disease and Transplantation; Division of Transplantation, Department of Surgery.
R Mark GhobrialSherrie and Alan Conover Center for Liver Disease and Transplantation; Division of Transplantation, Department of Surgery.
Howard P MonsourSherrie and Alan Conover Center for Liver Disease and Transplantation; Department of Gastroenterology and Transplant Hepatology; Department of Medicine, Houston Methodist Hospital, Houston, TX, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hepatocellular carcinoma (HCC) is the most common primary liver malignancy and is a leading cause of cancer-related death worldwide. In the United States, HCC is the ninth leading cause of cancer deaths. Despite advances in prevention techniques, screening, and new technologies in both diagnosis and treatment, incidence and mortality continue to rise. Cirrhosis remains the most important risk factor for the development of HCC regardless of etiology. Hepatitis B and C are independent risk factors for the development of cirrhosis. Alcohol consumption remains an important additional risk factor in the United States as alcohol abuse is five times higher than hepatitis C. Diagnosis is confirmed without pathologic confirmation. Screening includes both radiologic tests, such as ultrasound, computerized tomography, and magnetic resonance imaging, and serological markers such as α-fetoprotein at 6-month intervals. Multiple treatment modalities exist; however, only orthotopic liver transplantation (OLT) or surgical resection is curative. OLT is available for patients who meet or are downstaged into the Milan or University of San Francisco criteria. Additional treatment modalities include transarterial chemoembolization, radiofrequency ablation, microwave ablation, percutaneous ethanol injection, cryoablation, radiation therapy, systemic chemotherapy, and molecularly targeted therapies. Selection of a treatment modality is based on tumor size, location, extrahepatic spread, and underlying liver function. HCC is an aggressive cancer that occurs in the setting of cirrhosis and commonly presents in advanced stages. HCC can be prevented if there are appropriate measures taken, including hepatitis B virus vaccination, universal screening of blood products, use of safe injection practices, treatment and education of alcoholics and intravenous drug users, and initiation of antiviral therapy. Continued improvement in both surgical and nonsurgical approaches has demonstrated significant benefits in overall survival. While OLT remains the only curative surgical procedure, the shortage of available organs precludes this therapy for many patients with HCC.

Indexed as

cirrhosishepatocellular carcinomaorthotopic liver transplantationα-fetoprotein

Identifiers

PMID27785449
PMCPMC5063561

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.