Evidence map›Paper›PMID 35046521›Full record

ArticleBritish journal of cancer2022

Urine DNA biomarkers for hepatocellular carcinoma screening.

Amy K Kim, James P Hamilton, Selena Y Lin, Ting-Tsung Chang, Hie-Won Hann, Chi-Tan Hu, Yue Lou, Yih-Jyh Lin, Terence P Gade, Grace Park and 8 more

Open access · greenAbstract read
In one paragraph

Article in British journal of cancer, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
3.1field-weighted citation impact, top 7% 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

21 citing papers in PubMed, 35 citations in OpenAlex.

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  20. [Progress on the research of liver diseases in 2022].Zhonghua gan zang bing za zhi = Zhonghua ganzangbing zazhi = Chinese journal of hepatology · 2023
    Article
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

18 authors at 8 institutions in 2 countries.

Amy K Kim *Division of Gastroenterology and Hepatology, Department of Medicine, The Johns Hopkins University School of Medicine, Baltimore, MD, USA.
James P Hamilton *Division of Gastroenterology and Hepatology, Department of Medicine, The Johns Hopkins University School of Medicine, Baltimore, MD, USA.
Selena Y LinJBS Science, Inc., Doylestown, PA, USA.
Ting-Tsung ChangDepartment of Internal Medicine, National Cheng Kung University Hospital, College of Medicine, National Cheng Kung University, Tainan, Taiwan.
Hie-Won HannDepartment of Medicine, Division of Gastroenterology and Hepatology, Thomas Jefferson University Hospital, Philadelphia, PA, USA.
Chi-Tan HuDivision of Gastroenterology, Department of Internal Medicine, Hualien Tzu-Chi Hospital, Buddhist Tzu-Chi Medical Foundation and Tzu Chi University, Hualien, Taiwan.
Yue LouThe Baruch S. Blumberg Institute, Doylestown, PA, USA.
Yih-Jyh LinDepartment of Surgery, National Cheng Kung University Medical College and Hospital, Tainan, Taiwan, Republic of China.
Terence P GadeDepartment of Radiology, University of Pennsylvania College of Medicine, Philadelphia, PA, USA.
Grace ParkDepartment of Medicine, Division of Gastroenterology and Hepatology, Thomas Jefferson University Hospital, Philadelphia, PA, USA.
Harry LuuDivision of Gastroenterology and Hepatology, Department of Medicine, The Johns Hopkins University School of Medicine, Baltimore, MD, USA.
Tai-Jung LeeThe Baruch S. Blumberg Institute, Doylestown, PA, USA.
Jeremy WangJBS Science, Inc., Doylestown, PA, USA.
Dion ChenClinPharma Consulting, Inc, Phoenixville, PA, USA.
Michael G GogginsDivision of Gastroenterology and Hepatology, Department of Medicine, The Johns Hopkins University School of Medicine, Baltimore, MD, USA.ORCID http://orcid.org/0000-0002-4286-2296
Surbhi JainJBS Science, Inc., Doylestown, PA, USA.
Wei SongJBS Science, Inc., Doylestown, PA, USA.
Ying-Hsiu SuThe Baruch S. Blumberg Institute, Doylestown, PA, USA. Ying-hsiu.su@bblumberg.org.ORCID http://orcid.org/0000-0003-0969-0215
JBS Science (United States) · USJohns Hopkins University · USBaruch S. Blumberg Institute · USThomas Jefferson University Hospital · USNational Cheng Kung University · TWNational Cheng Kung University Hospital · TWTzu Chi University · TWUniversity of Pennsylvania · US

Funding

Development of a Urine Test for the Early Detection of Liver CancerR44CA165312 · NCI · JBS SCIENCE, INC. · PI LIN, SELENA · 2013 to 2020
$4.9M
Development of cell-free DNA assays for HCC screening and liquid biopsyR01CA202769 · NCI · BARUCH S. BLUMBERG INSTITUTE · PI SU, YING-HSIU · 2016 to 2020
$2.1M
Improved early prognostic algorithm for hepatocellulcar carcinomaK08CA237624 · NCI · JOHNS HOPKINS UNIVERSITY · PI KIM, AMY K · 2020 to 2024
$1.3M
Novel assay to detect integrated HBV DNA in urine of chronic hepatitis B patientsR43AI167169 · NIAID · JBS SCIENCE, INC. · PI LIN, SELENA · 2022 to 2023
$604k
Development of a Urine Test for the Early Detection of Liver CancerR43CA165312 · NCI · JBS SCIENCE, INC. · PI SONG, WEI · 2012 to 2012
$247k
NCI NIH HHS K08 CA237624NCI NIH HHS R01 CA202769NCI NIH HHS R43 CA165312NCI NIH HHS R44 CA165312NIAID NIH HHS R43 AI167169
6 · The paper itself

Abstract

backgroundHepatocellular carcinoma (HCC) occurs in a well-defined high-risk patient population, but better screening tests are needed to improve sensitivity and efficacy. Therefore, we investigated the use of urine circulating tumour DNA (ctDNA) as a screening test.

methodsCandidate markers in urine were selected from HCC and controls. We then enrolled 609 patients from five medical centres to test the selected urine panel. A two-stage model was developed to combine AFP and urine panel as a screening test.

resultsMutated TP53, and methylated RASSF1a, and GSTP1 were selected as the urine panel markers. Serum AFP outperformed the urine panel among all cases of HCC, but the urine panel identified 49% of HCC cases with low AFP < 20 ng/ml. Using the two-stage model, the combined AFP and urine panel identified 148 of the 186 HCC cases (79.6% sensitivity at 90% specificity), which was 30% more than the cases detected with serum AFP alone. It also increased early-stage HCC detection from 62% to 92% (BCLC stage 0), and 40% to 77% (BCLC stage A).

conclusionUrine ctDNA has promising diagnostic utility in patients in HCC, especially in those with low AFP and can be used as a potential non-invasive HCC screening test.

Indexed as

Carcinoma, HepatocellularCirculating Tumor DNALiver Neoplasmsalpha-FetoproteinsBiomarkers, TumorHumansalpha-FetoproteinsBiomarkers, TumorCirculating Tumor DNA

Identifiers

PMID35046521
PMCPMC9091244
OpenAlexW4206146888

What OpenQuestion holds

Textmetadata
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.