Evidence map›Paper›PMID 37078924›Full record

ArticleCancer medicine2023

Hepatocellular carcinoma in patients cured of chronic hepatitis C: Minimal steatosis.

Chiara Rocha, Erin H Doyle, Chip A Bowman, M-Isabel Fiel, Ashley E Stueck, Nicolas Goossens, Kian Bichoupan, Neal Patel, James F Crismale, Jasnit Makkar and 6 more

Open access · goldAbstract read
In one paragraph

Article in Cancer medicine, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
2.1field-weighted citation impact, top 12% 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

7 citing papers in PubMed, 10 citations in OpenAlex.

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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

16 authors at 7 institutions in 2 countries.

Chiara RochaDepartment of Surgery-Transplant Division, Icahn School of Medicine at Mount Sinai, New York, New York, USA.
Erin H DoyleDivision of Liver Diseases, Department of Medicine, Icahn School of Medicine at Mount Sinai School, New York, New York, USA.
Chip A BowmanDepartment of Medicine, Icahn School of Medicine at Mount Sinai, New York, New York, USA.ORCID 0000-0001-8293-0145
M-Isabel FielDepartment of Pathology, Icahn School of Medicine at Mount Sinai, New York, New York, USA.
Ashley E StueckDepartment of Pathology, Dalhousie University, Halifax, Nova Scotia, Canada.
Nicolas GoossensDivision of Liver Diseases, Department of Medicine, Tisch Cancer Institute, Icahn School of Medicine at Mount Sinai, New York, New York, USA.
Kian BichoupanDivision of Liver Diseases, Department of Medicine, Icahn School of Medicine at Mount Sinai, New York, New York, USA.
Neal PatelDivision of Gastroenterology, Department of Medicine, Nuvance Health Danbury Hospital, Danbury, CT, USA.
James F CrismaleDivision of Liver Diseases, Department of Medicine, Icahn School of Medicine at Mount Sinai, New York, New York, USA.
Jasnit MakkarDepartment of Radiology, Columbia University, New York, New York, USA.
Sara LewisDepartment of Radiology, Icahn School of Medicine at Mount Sinai, New York, New York, USA.
Ponni V PerumalswamiDepartment of Medicine, University of Michigan, Ann Arbor, Michigan, USA.
Thomas D SchianoDivision of Liver Diseases, Department of Medicine, Icahn School of Medicine at Mount Sinai, New York, New York, USA.
Yujin HoshidaDepartment of Internal Medicine, University of Texas Southwestern Medical Center, Dallas, Texas, USA.
Myron SchwartzDepartment of Surgery, Icahn School of Medicine at Mount Sinai, New York, New York, USA.
Andrea D BranchDivision of Liver Diseases, Department of Medicine, Icahn School of Medicine at Mount Sinai, New York, New York, USA.
Icahn School of Medicine at Mount Sinai · USColumbia University · USDalhousie University · CADanbury Hospital · USThe University of Texas Southwestern Medical Center · USTisch Hospital · USUniversity of Michigan · US

Funding

Trial of Statins for Chemoprevention in Hepatocellular CarcinomaR01CA255621 · NCI · MASSACHUSETTS GENERAL HOSPITAL · PI CHUNG, RAYMOND T, HOSHIDA, YUJIN · 2021 to 2025
$3.6M
Reverse-engineering precision liver cancer chemopreventionR01CA233794 · NCI · UT SOUTHWESTERN MEDICAL CENTER · PI HOSHIDA, YUJIN · 2019 to 2023
$3.5M
Optimizing Vitamin D Treatment in HIV/AIDS: An RCTR01DA031095 · NIDA · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI BRANCH, ANDREA D., DIETERICH, DOUGLAS THOMAS · 2010 to 2014
$3.3M
Molecular Prognostic Indicators in Liver Cirrhosis and CancerR01DK099558 · NIDDK · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI HOSHIDA, YUJIN · 2013 to 2016
$2.6M
Clinical Outcomes and the HCV Core GeneR01DK090317 · NIDDK · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI BRANCH, ANDREA D. · 2010 to 2014
$2.0M
NCI NIH HHS R01 CA233794NCI NIH HHS R01 CA255621NIDA NIH HHS R01 DA031095NIDDK NIH HHS R01 DK090317NIDDK NIH HHS R01 DK099558
6 · The paper itself

Abstract

backgroundSuccessful treatment of hepatitis C reduces liver inflammation and fibrosis; however, patients remain at risk of developing hepatocellular carcinoma (HCC).

aimsTo identify risk factors for new-onset HCC in patients cured of hepatitis C.

methodsImaging, histological, and clinical data on patients whose first HCC was diagnosed >12 months of post-SVR were analyzed. Histology of 20 nontumor tissues was analyzed in a blinded manner using the Knodel/Ishak/HAI system for necroinflammation and fibrosis/cirrhosis stage and the Brunt system for steatosis/steatohepatitis. Factors associated with post-SVR HCC were identified by comparison with HALT-C participants who did not develop post-SVR HCC.

resultsHepatocellular carcinoma was diagnosed in 54 patients (45 M/9F), a median of 6 years of post-SVR [interquartile range (IQR) =1.4-10y] at a median age of 61 years (IQR, 59-67). Approximately one-third lacked cirrhosis, and only 11% had steatosis on imaging. The majority (60%) had no steatosis/steatohepatitis in histopathology. The median HAI score was 3 (1.25-4), indicating mild necroinflammation. In a multivariable logistic regression model, post-SVR HCC was positively associated with non-Caucasian race (p = 0.03), smoking (p = 0.03), age > 60 years at HCC diagnosis (p = 0.03), albumin<3.5 g/dL (p = 0.02), AST/ALT>1 (p = 0.05), and platelets <100 × 10

conclusionsOne-third of patients with post-SVR HCC did not have liver cirrhosis; most had no steatosis/steatohepatitis. Hepatocellular carcinomas were more advanced in noncirrhotic patients. Results support AFP as a promising marker of post-SVR HCC risk.

Indexed as

Carcinoma, HepatocellularFatty LiverHepatitis CHepatitis C, ChronicLiver NeoplasmsAgedAntiviral AgentsHepacivirusHumansLiver CirrhosisMiddle AgedRisk FactorsSustained Virologic ResponseAntiviral Agentsalpha-fetoproteinhepatitis C virushepatocellular carcinomasustained virological response

Identifiers

PMID37078924
PMCPMC10225173
OpenAlexW4366464281

What OpenQuestion holds

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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.