Evidence map›Paper›PMID 42109832›Full record

ArticleEClinicalMedicine2026

Economic evaluation of alternative hepatitis C treatment options: a post hoc analysis of the VIETNARMS trial.

Hugo C Turner, Sayara Ahmed, Huyen Anh Nguyen, Le Manh Hung, Jennifer Van Nuil, Dang Trong Thuan, SEARCH investigators, Nguyen Thanh Dung, Guy E Thwaites, Ann Sarah Walker and 3 more

Abstract read
In one paragraph

Article in EClinicalMedicine, 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

13 authors.

Hugo C TurnerMRC Centre for Global Infectious Disease Analysis, School of Public Health, Imperial College London, Norfolk Place, London, United Kingdom.
Sayara AhmedMRC Centre for Global Infectious Disease Analysis, School of Public Health, Imperial College London, Norfolk Place, London, United Kingdom.
Huyen Anh NguyenOxford University Clinical Research Unit, Wellcome Trust Major Overseas Programme, Ho Chi Minh City, Vietnam.
Le Manh HungHospital for Tropical Diseases, Ho Chi Minh City, Vietnam.
Jennifer Van NuilOxford University Clinical Research Unit, Wellcome Trust Major Overseas Programme, Ho Chi Minh City, Vietnam.
Dang Trong ThuanOxford University Clinical Research Unit, Wellcome Trust Major Overseas Programme, Ho Chi Minh City, Vietnam.
SEARCH investigators
Nguyen Thanh DungHospital for Tropical Diseases, Ho Chi Minh City, Vietnam.
Guy E ThwaitesOxford University Clinical Research Unit, Wellcome Trust Major Overseas Programme, Ho Chi Minh City, Vietnam.
Ann Sarah WalkerMRC Clinical Trial Unit at UCL, University College London, United Kingdom.
Nguyen Van Vinh ChauHospital for Tropical Diseases, Ho Chi Minh City, Vietnam.
Graham S CookeDepartment of Infectious Disease, Imperial College London, United Kingdom.
Timothy B HallettMRC Centre for Global Infectious Disease Analysis, School of Public Health, Imperial College London, Norfolk Place, London, United Kingdom.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Hepatitis C remains a leading cause of liver disease worldwide, and access to Direct-Acting Antiviral (DAA) treatment remains limited in many settings. Alternative treatment strategies that require fewer tablets and clinical visits could help improve equitable access, and new approaches have recently been found to be non-inferior in producing sustained viral suppression. Methods: We did a cost-minimization analysis of alternative treatment options for non-cirrhotic patients evaluated in the VIETNARMS trial (ISRCTN61522291), conducted between 19/06/2020 and 10/05/2023 in Vietnam. These were: (i) 'response guided' (which adjusts treatment duration based on 1-week viral load); (ii) 'induction maintenance' (which reduces the dosing frequency in later weeks of treatment); and (iii) 'Peg-IFN + DAA' (4 weeks of DAAs combined with four weekly doses of PEGylated interferon (Peg-IFN)). The primary outcome was the cost per cure. A disaggregated societal perspective was adopted, including stratification for the healthcare provider and patient costs. Findings: The three alternative treatment strategies were projected to have lower costs per cure than standard 12-week DAA treatment in the base-case scenario: US$202 (15%) less for 'response guided', US$234 (18%) less for 'induction maintenance', and US$163 (12%) less for 'Peg-IFN + DAA'. However, the potential for cost savings, and which strategy had the lowest cost per cure, depended on the assumed cost of DAA drugs: the strategy with the lowest cost per cure was generally 'induction maintenance' when DAA drug costs for a standard treatment course were under US$1000, but Peg-IFN + DAA when DAA costs exceeded US$1500. In some scenarios, lower costs per cure were achieved through reduced health system expenditures, despite increased costs to patients. Interpretation: Alternative strategies for Hepatitis C treatment could reduce costs for providers and patients. As this is highly dependent on the variable costs of DAAs, approaches should be fit carefully to the prevailing context. Funding: Wellcome Trust, Medical Research Council.

Indexed as

CostCost-minimization analysisDAAEconomic evaluationHepatitis CTreatment strategies

Identifiers

PMID42109832
PMCPMC13156567

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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.