Evidence map›Paper›PMID 35199349›Full record

ArticleStatistics in medicine2022

A multivariate parametric empirical Bayes screening approach for early detection of hepatocellular carcinoma using multiple longitudinal biomarkers.

Nabihah Tayob, Anna S F Lok, Ziding Feng

Abstract read
In one paragraph

Article in Statistics in medicine, 2022. 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
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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

3 authors.

Nabihah TayobDepartment of Data Science, Dana-Farber Cancer Institute, Boston, Massachusetts, USA.ORCID 0000-0001-6088-167X
Anna S F LokDepartment of Internal Medicine, University of Michigan, Ann Arbor, Michigan, USA.
Ziding FengBiostatistics Program, Fred Hutchinson Cancer Research Center, Seattle, Washington, USA.

Funding

The Early Detection Research Network: Data Management and Coordinating CenterU24CA086368 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI RUTH D ETZIONI, Ziding Feng · 2010 to 2026
$75.7M
Consortium on Translational Research in Early Detection of Liver Cancer:Data Management and Coordinating Center (DMCC)U24CA230144 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI Ziding Feng · 2018 to 2026
$5.8M
Training Program in Gastrointestinal EpidemiologyT32DK062708 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Peter D.R. Higgins, Elliot Tapper · 2003 to 2026
$3.9M
NOVEL STRATEGIES TO IMPROVE LIVER CANCER SURVEILLANCE UPTAKE AND EARLY DETECTIONU01CA230669 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI LOK, ANNA S.F., SU, GRACE L. · 2018 to 2022
$3.3M
Biomarker screening algorithms for the improved early detection of hepatocellular carcinomaR01CA230503 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI TAYOB, NABIHAH · 2019 to 2025
$1.6M
NCI NIH HHS R01 CA230503NCI NIH HHS R01CA230503NCI NIH HHS U01 CA230669NCI NIH HHS U01CA230669NCI NIH HHS U24 CA086368NCI NIH HHS U24CA086368NCI NIH HHS U24 CA230144NCI NIH HHS U24CA230144NIDDK NIH HHS T32 DK062708
6 · The paper itself

Abstract

The early detection of hepatocellular carcinoma (HCC) is critical to improving outcomes since advanced HCC has limited treatment options. Current guidelines recommend HCC ultrasound surveillance every 6 months in high-risk patients however the sensitivity for detecting early stage HCC in clinical practice is poor. Blood-based biomarkers are a promising direction since they are more easily standardized and less resource intensive. Combining of multiple biomarkers is more likely to achieve the sensitivity required for a clinically useful screening algorithm and the longitudinal trajectory of biomarkers contains valuable information that should be utilized. We propose a multivariate parametric empirical Bayes (mPEB) screening approach that defines personalized thresholds for each patient at each screening visit to identify significant deviations that trigger additional testing with more sensitive imaging. The Hepatitis C Antiviral Long-term Treatment against Cirrhosis (HALT-C) trial provides a valuable source of data to study HCC screening algorithms. We study the performance of the mPEB algorithm applied to serum

Indexed as

Carcinoma, HepatocellularLiver Neoplasmsalpha-FetoproteinsBayes TheoremBiomarkersBiomarkers, TumorHumansLiver CirrhosisSensitivity and Specificityalpha-FetoproteinsBiomarkersBiomarkers, Tumorbiomarkersearly detectionempirical Bayeslongitudinal screening historynumeric optimization

Identifiers

PMID35199349
PMCPMC9035119

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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.