Evidence map›Paper›PMID 41115581›Full record

ArticleClinical gastroenterology and hepatology : the official clinical practice journal of the American Gastroenterological Association2026

Recent Trends of Incidence, Mortality, Treatment, and Overall Survival of Hepatocellular Carcinoma in the United States.

Yi-Te Lee, Jasmine J Wang, Pojsakorn Danpanichkul, Hyun-Seok Kim, Alexander Kuo, Walid S Ayoub, Hirsh D Trivedi, Yun Wang, Aarshi Vipani, Paul Martin and 3 more

Abstract read
In one paragraph

Article in Clinical gastroenterology and hepatology : the official clinical practice journal of the American Gastroenterological Association, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–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

4 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Review
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

13 authors.

Yi-Te LeeDepartment of Medicine, Cedars-Sinai Medical Center, Los Angeles, California.
Jasmine J WangDepartment of Laboratory Medicine & Pathology, University of Washington, Seattle, Washington.
Pojsakorn DanpanichkulDepartment of Internal Medicine, Texas Tech University Health Sciences Center, Lubbock, Texas.
Hyun-Seok KimKarsh Division of Gastroenterology and Hepatology, Cedars-Sinai Medical Center, Los Angeles, California; Comprehensive Transplant Center, Cedars-Sinai Medical Center, Los Angeles, California.
Alexander KuoKarsh Division of Gastroenterology and Hepatology, Cedars-Sinai Medical Center, Los Angeles, California; Comprehensive Transplant Center, Cedars-Sinai Medical Center, Los Angeles, California.
Walid S AyoubKarsh Division of Gastroenterology and Hepatology, Cedars-Sinai Medical Center, Los Angeles, California; Comprehensive Transplant Center, Cedars-Sinai Medical Center, Los Angeles, California.
Hirsh D TrivediKarsh Division of Gastroenterology and Hepatology, Cedars-Sinai Medical Center, Los Angeles, California; Comprehensive Transplant Center, Cedars-Sinai Medical Center, Los Angeles, California.
Yun WangKarsh Division of Gastroenterology and Hepatology, Cedars-Sinai Medical Center, Los Angeles, California; Comprehensive Transplant Center, Cedars-Sinai Medical Center, Los Angeles, California.
Aarshi VipaniKarsh Division of Gastroenterology and Hepatology, Cedars-Sinai Medical Center, Los Angeles, California; Comprehensive Transplant Center, Cedars-Sinai Medical Center, Los Angeles, California.
Paul MartinKarsh Division of Gastroenterology and Hepatology, Cedars-Sinai Medical Center, Los Angeles, California; Comprehensive Transplant Center, Cedars-Sinai Medical Center, Los Angeles, California.
Cristina R FerroneDepartment of Surgery, Cedars-Sinai Medical Center, Los Angeles, California.
Amit G SingalDivision of Digestive and Liver Diseases, University of Texas Southwestern Medical Center, Dallas, Texas.
Ju Dong YangKarsh Division of Gastroenterology and Hepatology, Cedars-Sinai Medical Center, Los Angeles, California; Comprehensive Transplant Center, Cedars-Sinai Medical Center, Los Angeles, California; Samuel Oschin Comprehensive Cancer Institute, Cedars-Sinai Medical Center, Los Angeles, California. Electronic address: judong.yang@cshs.org.

Funding

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
Multi-level Evaluation of Racial/ethnic Disparities in Liver Disease OutcomesR01CA256977 · NCI · BAYLOR COLLEGE OF MEDICINE · PI KANWAL, FASIHA, SINGAL, AMIT · 2021 to 2025
$3.0M
Novel circulating biomarker digital scores for assessing treatment response in liver cancerK08CA259534 · NCI · CEDARS-SINAI MEDICAL CENTER · PI YANG, JU DONG · 2022 to 2024
$807k
Novel circulating biomarker digital scores for assessing treatment response in liver cancerR21CA280444 · NCI · CEDARS-SINAI MEDICAL CENTER · PI YANG, JU DONG, ZHU, YAZHEN · 2023 to 2023
$436k
NCI NIH HHS K08 CA259534NCI NIH HHS R01 CA256977NCI NIH HHS R21 CA280444NIMHD NIH HHS R01 MD012565
6 · The paper itself

Abstract

BACKGROUND &

aimsWith the COVID-19 pandemic, changes in liver disease etiologies, and expanded therapeutic options for hepatocellular carcinoma (HCC), recent trends in the incidence and mortality rates, tumor burden, treatment, and overall survival (OS) of HCC in the United States warrant investigation.

methodsThe Surveillance, Epidemiology, and End Results database was used to assess trends in incidence, mortality, tumor burden, and OS. Logistic regression analysis identified factors associated with curative treatment and no treatment, whereas Cox regression analysis identified factors associated with OS.

resultsHCC incidence rates increased from 2000 to 2014, plateaued from 2014 to 2019, and declined from 2019 to 2022 (annual percent change, -3.74%; 95% confidence interval [CI], -4.65% to -2.39%; P < .001). Incidence-based mortality increased from 2000 to 2013 and then plateaued through 2022. Compared with 2016 to 2019, the COVID-19 pandemic (2020-2022) was associated with lower odds of curative treatment (adjusted odds ratio [aOR], 0.87; 95% CI, 0.82-0.91; P < .001) and increased likelihood of no treatment (aOR, 1.48; 95% CI, 1.41-1.54; P < .001). OS improved from 2000 to 2019 but did not significantly change during 2020 to 2022 (vs 2016-2019: adjusted hazard ratio, 0.98; 95% CI, 0.95-1.01; P = .2). Conversely, OS improved among patients <50 years old, those with distant HCC, and non-Hispanic Blacks. Non-Hispanic Black race was not associated with worse survival (adjusted hazard ratio, 1.01; 95% CI, 0.99-1.03; P = .4).

conclusionsHCC incidence rates have started to decline, and incidence-based mortality has plateaued. Given lower early-stage detection and curative treatments during the COVID-19 pandemic, longer-term follow-up is warranted to assess the impact on survival. The reduced survival disparities between non-Hispanic Black and White patients may reflect improved equitable medical access.

Indexed as

Carcinoma, HepatocellularCOVID-19Liver NeoplasmsAgedFemaleHumansIncidenceMaleMiddle AgedSEER ProgramSurvival RateUnited StatesEpidemiologyHepatocellular CarcinomaOverall SurvivalTreatment ReceiptTrend Analysis

Identifiers

PMID41115581
PMCPMC13035008

What OpenQuestion holds

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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.