Evidence map›Paper›PMID 36302828›Full record

ArticleScientific reports2022

Evaluation of machine learning algorithms for predicting direct-acting antiviral treatment failure among patients with chronic hepatitis C infection.

Haesuk Park, Wei-Hsuan Lo-Ciganic, James Huang, Yonghui Wu, Linda Henry, Joy Peter, Mark Sulkowski, David R Nelson

Abstract read
In one paragraph

Article in Scientific reports, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Article
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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

8 authors.

Haesuk ParkDepartment of Pharmaceutical Outcomes and Policy, College of Pharmacy, University of Florida, HPNP Building Room 3325, 1225 Center Drive, Gainesville, FL, 32610, USA. hpark@cop.ufl.edu.
Wei-Hsuan Lo-CiganicDepartment of Pharmaceutical Outcomes and Policy, College of Pharmacy, University of Florida, HPNP Building Room 3325, 1225 Center Drive, Gainesville, FL, 32610, USA.
James HuangDepartment of Pharmaceutical Outcomes and Policy, College of Pharmacy, University of Florida, HPNP Building Room 3325, 1225 Center Drive, Gainesville, FL, 32610, USA.
Yonghui WuHealth Outcomes & Biomedical Informatics, College of Medicine, University of Florida, Gainesville, FL, USA.
Linda HenryDepartment of Pharmaceutical Outcomes and Policy, College of Pharmacy, University of Florida, HPNP Building Room 3325, 1225 Center Drive, Gainesville, FL, 32610, USA.
Joy PeterDepartment of Medicine, University of Florida, Gainesville, FL, USA.
Mark SulkowskiJohns Hopkins University School of Medicine, Baltimore, MD, USA.
David R NelsonDepartment of Medicine, University of Florida, Gainesville, FL, USA.

Funding

Patient Oriented Research in Hepatitis C-infected Injection Drug UsersK24DA034621 · NIDA · JOHNS HOPKINS UNIVERSITY · PI SULKOWSKI, MARK SEBASTIAN · 2012 to 2022
$1.2M
Medicaid Prior Authorization Policies for Chronic Hepatitis C Treatment in Vulnerable PopulationsK01DA045618 · NIDA · UNIVERSITY OF FLORIDA · PI PARK, HAESUK · 2018 to 2022
$648k
NIDA NIH HHS K01 DA045618NIDA NIH HHS K24 DA034621
6 · The paper itself

Abstract

Despite the availability of efficacious direct-acting antiviral (DAA) therapy, the number of people infected with hepatitis C virus (HCV) continues to rise, and HCV remains a leading cause of liver-related morbidity, liver transplantation, and mortality. We developed and validated machine learning (ML) algorithms to predict DAA treatment failure. Using the HCV-TARGET registry of adults who initiated all-oral DAA treatment, we developed elastic net (EN), random forest (RF), gradient boosting machine (GBM), and feedforward neural network (FNN) ML algorithms. Model performances were compared with multivariable logistic regression (MLR) by assessing C statistics and other prediction evaluation metrics. Among 6525 HCV-infected adults, 308 patients (4.7%) experienced DAA treatment failure. ML models performed similarly in predicting DAA treatment failure (C statistic [95% CI]: EN, 0.74 [0.69-0.79]; RF, 0.74 [0.69-0.80]; GBM, 0.72 [0.67-0.78]; FNN, 0.75 [0.70-0.80]), and all 4 outperformed MLR (C statistic [95% CI]: 0.51 [0.46-0.57]), and EN used the fewest predictors (n = 27). With Youden index, the EN had 58.4% sensitivity and 77.8% specificity, and nine patients were needed to evaluate to identify 1 DAA treatment failure. Over 60% treatment failure were classified in top three risk decile subgroups. EN-identified predictors included male sex, treatment < 8 weeks, treatment discontinuation due to adverse events, albumin level < 3.5 g/dL, total bilirubin level > 1.2 g/dL, advanced liver disease, and use of tobacco, alcohol, or vitamins. Addressing modifiable factors of DAA treatment failure may reduce the burden of retreatment. Machine learning algorithms have the potential to inform public health policies regarding curative treatment of HCV.

Indexed as

Hepatitis CHepatitis C, ChronicAdultAlgorithmsAntiviral AgentsHepacivirusHumansMachine LearningMaleTreatment FailureAntiviral Agents

Identifiers

PMID36302828
PMCPMC9613877

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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.