Evidence map›Paper›PMID 42745531›Full record

ArticleJournal of viral hepatitis2026

Development of a Machine Learning Model to Predict Short Duration HCV Treatment Response.

Joanne M Carson, Sebastiano Barbieri, Andrey Verich, Elise Tu, Andrew Lloyd, Gregory J Dore, Gail V Matthews, Marianne Martinello

Abstract read
In one paragraph

Article in Journal of viral hepatitis, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Joanne M CarsonKirby Institute, University of New South Wales, Sydney, Australia.ORCID https://orcid.org/0000-0001-8043-0200
Sebastiano BarbieriQueensland Digital Health Centre, University of Queensland, Brisbane, Australia.ORCID https://orcid.org/0000-0002-5919-372X
Andrey VerichKirby Institute, University of New South Wales, Sydney, Australia.
Elise TuKirby Institute, University of New South Wales, Sydney, Australia.ORCID https://orcid.org/0000-0001-5762-3012
Andrew LloydKirby Institute, University of New South Wales, Sydney, Australia.ORCID https://orcid.org/0000-0001-6277-8887
Gregory J DoreKirby Institute, University of New South Wales, Sydney, Australia.ORCID https://orcid.org/0000-0002-4741-2622
Gail V MatthewsKirby Institute, University of New South Wales, Sydney, Australia.
Marianne MartinelloKirby Institute, University of New South Wales, Sydney, Australia.ORCID https://orcid.org/0000-0001-9444-0186

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Standard durations of direct acting antivirals (DAAs; 8-12 weeks) can be a barrier to HCV treatment initiation and completion among marginalized populations. This study developed and internally validated a machine learning model to predict short-duration (4-6 weeks) DAA response using baseline clinical factors with potential to improve treatment uptake, cost-effectiveness and health system efficiency. Baseline data from several short-duration DAA clinical trials and treatment discontinuations from real-world cohort studies were used. Multiple machine learning models were evaluated. Nested cross-validation was employed to optimize model hyperparameters and assess performance. Clinical utility was evaluated using Area Under Receiver Operator Characteristics (AUROC), Area Under Precision Recall Curve (AUPRC) and Matthews Correlation Coefficient (MCC). Threshold optimisation strategies were applied to balance model accuracy and DAA costs. Statistical analyses were conducted to estimate HCV RNA cutoffs predictive of treatment failure. Of 264 participants receiving short-duration DAAs (median 42 days; IQR 28-42), 94 (36%) experienced treatment failure. Predictors of failure included shorter durations, higher HCV RNA, higher AST-ALT ratio, genotype 3 and DAA class. The Elastic Net (regularized logistic regression) model demonstrated strong performance (AUROC: 83%; AUPRC: 73%). The Youden Index threshold balanced sensitivity (81%) and specificity (76%) with MCC of 0.56. A cost-optimized threshold, prioritizing retreatment minimization, achieved high sensitivity (98%) but reduced specificity (51%). HCV RNA cutoffs predictive of treatment failure were higher for protease+NS5A than NS5A + NS5B inhibitor regimens. Predictive models using baseline clinical data can identify individuals likely to respond to short-duration DAAs. Such models, if externally validated in larger and more diverse datasets, could facilitate HCV elimination efforts by improving treatment uptake, particularly for people who inject drugs, people experiencing homelessness or incarceration.

Indexed as

Antiviral AgentsHepatitis C, ChronicMachine LearningFemaleHepacivirusHumansMaleMiddle AgedPrediction AlgorithmsPredictive Learning ModelsTime FactorsTreatment FailureTreatment OutcomeAntiviral Agentsartificial intelligenceDAAHCVmachine learningmodellingpersonalized medicinetreatment failure

Identifiers

PMID42745531
PMCPMC13579082

What OpenQuestion holds

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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.