Evidence map›Paper›PMID 40874910›Full record

ArticleCancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology2025

Antiviral Treatment Reduces Risk of Development of Lung Cancer and Non-Hodgkin Lymphoma in Patients with Chronic Hepatitis C.

Meng-Hua Tao, Trueman Wu, Stuart C Gordon, Yueren Zhou, Loralee B Rupp, Sheri Trudeau, Mark A Schmidt, Yihe G Daida, Mei Lu

Abstract read
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In one paragraph

Article in Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology, 2025. 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. Article
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors.

Meng-Hua TaoDepartment of Public Health Sciences, Henry Ford Health, Detroit, Michigan.ORCID 0000-0001-9944-2105
Trueman WuDepartment of Public Health Sciences, Henry Ford Health, Detroit, Michigan.ORCID 0009-0000-8237-0862
Stuart C GordonDepartment of Gastroenterology and Hepatology, Henry Ford Health, Detroit, Michigan.ORCID 0000-0001-8666-3849
Yueren ZhouDepartment of Public Health Sciences, Henry Ford Health, Detroit, Michigan.ORCID 0000-0002-8222-8644
Loralee B RuppCenter for Health Policy and Health Services Research, Henry Ford Health, Detroit, Michigan.ORCID 0000-0002-2048-5100
Sheri TrudeauDepartment of Public Health Sciences, Henry Ford Health, Detroit, Michigan.ORCID 0000-0003-1280-0833
Mark A SchmidtCenter for Health Research, Portland, Oregon.ORCID 0000-0002-7440-7183
Yihe G DaidaCenter for Integrated Health Care Research, Honolulu, Hawaii.ORCID 0000-0003-1628-0476
Mei LuDepartment of Public Health Sciences, Henry Ford Health, Detroit, Michigan.ORCID 0000-0002-3313-6428

Funding

Centers for Disease Control and Prevention (CDC) PS16-002
6 · The paper itself

Abstract

backgroundAntiviral treatment for hepatitis C virus (HCV) has been shown to reduce risk of liver cancer, but there are few studies on its impact on the risk of non-liver cancers. We used a large cohort of patients with HCV with extensive follow-up to investigate whether receipt of antiviral therapy affects the risk of extrahepatic cancers.

methodsA total of 17,485 patients with HCV were followed until incidence of lung cancer, non-Hodgkin lymphoma (NHL), breast or prostate cancer, death, or last follow-up. We used multivariable modeling with time-varying covariates and propensity scores to adjust for treatment selection bias; we also applied generalized estimating equations with a multinominal link function for discrete time-to-event data. Death was considered a competing risk.

resultsAfter 15 years of follow-up, we identified 408 incident cases of cancers, namely 140 lung, 72 NHL, 81 breast (female), and 115 prostate cancer cases. Compared with no treatment, patients who receive either direct-acting antivirals or IFN-based treatment had significantly lower risk of lung cancer [HR = 0.35, 95% confidence interval, 0.24-0.52 for achieving sustained virologic response (SVR); HR = 0.34, 95% confidence interval, 0.21-0.55 for treatment failure]. Risk of NHL was reduced only among patients who achieved SVR. There were no significant associations between antiviral therapy and risks of breast and prostate cancers.

conclusionsAntiviral treatment for HCV independently reduced the risk of lung cancer, whereas the protective association with NHL was limited to patients achieving SVRs. IMPACT: Our findings support the importance of timely initiation antiviral therapy in patients with chronic HCV.

Indexed as

Antiviral AgentsHepatitis C, ChronicLung NeoplasmsLymphoma, Non-HodgkinAdultAgedFemaleFollow-Up StudiesHumansIncidenceMaleMiddle AgedRisk FactorsAntiviral Agents

Identifiers

What OpenQuestion holds

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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.