Evidence map›Paper›PMID 32017165›Full record

ArticleHepatology (Baltimore, Md.)2020

Hepatocellular Carcinoma Demonstrates Heterogeneous Growth Patterns in a Multicenter Cohort of Patients With Cirrhosis.

Nicole E Rich, Binu V John, Neehar D Parikh, Ian Rowe, Neil Mehta, Gaurav Khatri, Smitha M Thomas, Munazza Anis, Mishal Mendiratta-Lala, Christopher Hernandez and 11 more

Open access · bronzeAbstract readMulticenter Study
In one paragraph

Article in Hepatology (Baltimore, Md.), 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 91 papers, 9 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
91citing papers in PubMed, 9 pooled it
14.5field-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.

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

91 citing papers in PubMed, 9 syntheses or guidelines pooled it, 131 citations in OpenAlex.

  1. Racial and Ethnic Disparities in Survival among Patients with Cholangiocarcinoma in the United States: A Systematic Review and Meta-analysis.Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology · 2025
    Pooled it
  2. Racial and Ethnic Disparities in Hepatocellular Carcinoma Treatment Receipt in the United States: A Systematic Review and Meta-Analysis.Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology · 2024
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  5. Racial and Ethnic Disparities in Survival Among Patients With Hepatocellular Carcinoma in the United States: A Systematic Review and Meta-Analysis.Clinical gastroenterology and hepatology : the official clinical practice journal of the American Gastroenterological Association · 2022
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  15. [Chinese expert consensus on the use of standardized second-line drugs for primary hepatocellular carcinoma].Zhonghua gan zang bing za zhi = Zhonghua ganzangbing zazhi = Chinese journal of hepatology · 2026
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31 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

21 authors at 7 institutions in 2 countries.

Nicole E RichDivision of Digestive and Liver Diseases, Department of Internal Medicine, University of Texas Southwestern Medical Center, Dallas, TX.ORCID 0000-0003-2740-8818
Binu V JohnDivision of Gastroenterology and Hepatology, McGuire VA Medical Center, Richmond, VA.
Neehar D ParikhDivision of Gastroenterology and Hepatology, University of Michigan, Ann Arbor, MI.ORCID 0000-0002-5874-9933
Ian RoweLeeds Institute for Data Analytics, University of Leeds, Leeds, United Kingdom.ORCID 0000-0003-1288-0749
Neil MehtaDivision of Gastroenterology, Department of Medicine, University of California San Francisco, San Francisco, CA.ORCID 0000-0002-9476-468X
Gaurav KhatriDepartment of Radiology, University of Texas Southwestern Medical Center, Dallas, TX.
Smitha M ThomasDepartment of Radiology, McGuire VA Medical Center, Richmond, VA.
Munazza AnisDepartment of Radiology, McGuire VA Medical Center, Richmond, VA.
Mishal Mendiratta-LalaDepartment of Radiology, University of Michigan, Ann Arbor, MI.
Christopher HernandezDivision of Digestive and Liver Diseases, Department of Internal Medicine, University of Texas Southwestern Medical Center, Dallas, TX.
Mobolaji OdewoleDivision of Digestive and Liver Diseases, Department of Internal Medicine, University of Texas Southwestern Medical Center, Dallas, TX.
Latha T SundaramDivision of Gastroenterology and Hepatology, McGuire VA Medical Center, Richmond, VA.
Venkata R KonjetiDivision of Gastroenterology and Hepatology, McGuire VA Medical Center, Richmond, VA.
Shishir ShettyCentre for Liver Research, University of Birmingham and Liver and Hepatobiliary Unit, Queen Elizabeth Hospital Birmingham, Birmingham, United Kingdom.
Tahir ShahLiver and Hepatobiliary Unit, Queen Elizabeth Hospital Birmingham, Birmingham, United Kingdom.
Hao ZhuChildren's Research Institute, University of Texas Southwestern Medical Center, Dallas, TX.ORCID 0000-0002-8417-9698
Adam C YoppDepartment of Surgery, University of Texas Southwestern Medical Center, Dallas, TX.
Yujin HoshidaDivision of Digestive and Liver Diseases, Department of Internal Medicine, University of Texas Southwestern Medical Center, Dallas, TX.
Francis Y YaoDivision of Gastroenterology, Department of Medicine, University of California San Francisco, San Francisco, CA.
Jorge A MarreroDivision of Digestive and Liver Diseases, Department of Internal Medicine, University of Texas Southwestern Medical Center, Dallas, TX.
Amit G SingalDivision of Digestive and Liver Diseases, Department of Internal Medicine, University of Texas Southwestern Medical Center, Dallas, TX.
The University of Texas Southwestern Medical Center · USHunter Holmes McGuire VA Medical Center · USQueen Elizabeth Hospital Birmingham · GBUniversity of California, San Francisco · USUniversity of Michigan · USUniversity of Leeds · GBVirginia Commonwealth University · US

Funding

UT Southwestern Center for Translational Medicine (UL1/KL2/TL1)UL1TR001105 · NCATS · UT SOUTHWESTERN MEDICAL CENTER · PI TOTO, ROBERT DANIEL · 2013 to 2017
$24.5M
Multilevel factors for racial/ethnic and socioeconomic disparities in prognosis of hepatocellular carcinomaR01MD012565 · NIMHD · UT SOUTHWESTERN MEDICAL CENTER · PI SINGAL, AMIT, YOPP, ADAM · 2018 to 2022
$4.3M
Precision Risk Stratification and Screening for HCC among Patients with Cirrhosis in the United StatesU01CA230694 · NCI · UT SOUTHWESTERN MEDICAL CENTER · PI SINGAL, AMIT · 2018 to 2022
$3.5M
Reverse-engineering precision liver cancer chemopreventionR01CA233794 · NCI · UT SOUTHWESTERN MEDICAL CENTER · PI HOSHIDA, YUJIN · 2019 to 2023
$3.5M
NCATS NIH HHS UL1 TR001105NCI NIH HHS R01 CA233794NCI NIH HHS U01 CA230694NIH HHS NCI U01 CA230694NIH HHS R01 MD012565NIH HHS UL1-TR001105NIMHD NIH HHS R01 MD012565
6 · The paper itself

Abstract

BACKGROUND AND

aimsThere are limited data on hepatocellular carcinoma (HCC) growth patterns, particularly in Western cohorts, despite implications for surveillance, prognosis, and treatment. Our study's aim was to quantify tumor doubling time (TDT) and identify correlates associated with indolent and rapid growth. APPROACH AND

resultsWe performed a retrospective multicenter cohort study of patients with cirrhosis diagnosed with HCC from 2008 to 2017 at six US and European health systems with two or more contrast-enhanced imaging studies performed ≥ 30 days apart prior to HCC treatment. Radiologists independently measured tumors in three dimensions to calculate TDT and specific growth rate (SGR). We used multivariable ordinal logistic regression to identify factors associated with indolent (TDT > 365 days) and rapid (TDT < 90 days) tumor growth. In the primary cohort (n = 242 patients from four centers), median TDT was 229 days (interquartile range [IQR], 89-627) and median SGR was 0.3% per day (IQR, 0.1%-0.8%). Over one-third (38%) of HCCs had indolent growth, 36.8% intermediate growth, and 25.2% rapid growth. In multivariable analysis, indolent growth was associated with larger tumor diameter (odds ratio [OR], 1.15, 95% confidence interval [CI], 1.03-1.30) and alpha-fetoprotein < 20 ng/mL (OR, 1.90; 95% CI, 1.12-3.21). Indolent growth was more common in nonviral than viral cirrhosis (50.9% versus 32.1%), particularly in patients with T1 HCC (OR, 3.41; 95% CI, 1.08-10.80). Median TDT (169 days; IQR 74-408 days) and SGR (0.4% per day) were similar in an independent cohort (n = 176 patients from two centers).

conclusionsIn a large Western cohort of patients with HCC, we found heterogeneous tumor growth patterns, with one-fourth exhibiting rapid growth and over one-third having indolent growth. Better understanding different tumor growth patterns may facilitate a precision approach to prognostication and treatment.

Indexed as

Agedalpha-FetoproteinsCarcinoma, HepatocellularFemaleHumansLiverLiver CirrhosisLiver NeoplasmsMaleMiddle AgedNeoplasm StagingOdds RatioPrognosisProspective StudiesRetrospective StudiesRisk FactorsAFP protein, humanalpha-Fetoproteins

Identifiers

PMID32017165
PMCPMC7398837
OpenAlexW3004642728

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Registered trials

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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.