Evidence map›Paper›PMID 40844681›Full record

ArticleInfectious diseases and therapy2025

Hepatocellular Carcinoma Recurrence in Patients with Chronic Hepatitis C Infection Treated with Direct-Acting Antivirals: A Systematic Review and Meta-Analysis.

Kristina Lindsley, Margaret Burroughs, Candido Hernandez-Lopez, Yi Wang, John Marcinak, Stephanie E Chiuve, Barbara A Haber, Jennifer Uyei, Soodabeh Navadeh, Giuseppe De Marco and 1 more

Abstract read
In one paragraph

Article in Infectious diseases and therapy, 2025. 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

11 authors.

Kristina LindsleyIQVIA, Inc. Evidence Synthesis, 2400 Ellis Road, Durham, NC, 27709, USA. Kristina.Lindsley@IQVIA.com.ORCID http://orcid.org/0000-0003-4536-9920
Margaret BurroughsAbbVie, Inc, North Chicago, IL, 60064, USA.
Candido Hernandez-LopezGilead Sciences SA, 28033, Madrid, Spain.
Yi WangIQVIA, Advanced Analytics, King of Prussia, PA, 19087, USA.
John MarcinakAbbVie, Inc, North Chicago, IL, 60064, USA.
Stephanie E ChiuveAbbVie, Inc, North Chicago, IL, 60064, USA.
Barbara A HaberMerck & Co., Inc, MRL, Global Clinical Development, Rahway, NJ, 07065, USA.
Jennifer UyeiEvidence Synthesis, IQVIA, San Francisco, CA, 94105, USA.
Soodabeh NavadehGilead Sciences, Inc, Foster City, CA, 94404, USA.
Giuseppe De MarcoGilead Sciences International Ltd, Cambridge, CB21 6GT, UK.
Deanna D HillMerck & Co., Inc, MRL, BARDS Epidemiology, Rahway, NJ, 07065, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionReports of direct-acting antivirals (DAA) use for chronic hepatitis C virus (HCV) infection after successful treatment of hepatocellular carcinoma (HCC) have suggested higher rates of HCC recurrence. However, other studies have indicated no increased risk of HCC recurrence.

methodsTo estimate the comparative risk of early HCC recurrence in adults successfully treated for HCC and subsequently treated with interferon (IFN)-free DAAs versus not treated with DAAs for chronic HCV, we conducted a systematic literature review and meta-analysis following established guidelines.

resultsForty-one cohort studies (10,563 total participants) were identified. The following mutually exclusive comparisons to DAA therapy were determined: IFN-based therapy; no DAA; and no antiviral therapy. Random effects meta-analysis results indicated no increased risk of HCC recurrence with IFN-free DAA therapy when compared with IFN (combined risk ratio (RR) 1.29 [95% CI 0.69, 2.40] at 12 months, 0.88 [95% CI 0.56, 1.39] at 24 months, and 0.67 [95% CI 0.51, 0.88] at longest follow-up), no DAA (combined RR 0.55 [95% CI 0.25, 1.23] at 12 months, 0.67 [95% CI 0.51, 0.86] at 24 months and 0.72 [95% CI 0.61, 0.85] at longest follow-up), or no antiviral therapy (combined RR 0.95 [95% CI 0.76, 1.20] at 12 months, 0.48 [95% CI 0.11, 2.12] at 24 months, and 0.42 [95% CI 0.24, 0.73] at longest follow-up). Results were confirmed in sensitivity analyses.

conclusionsThere is no evidence to suggest that DAA therapy has a higher risk of early HCC recurrence when compared with IFN, no DAA, or no antiviral therapy at any timepoint analyzed. Hence the benefit-risk profile of DAAs in HCV remains positive in relation to the risk of early HCC recurrence.

Indexed as

Chronic hepatitis CDirect-acting antiviralsHepatitis CHepatocellular carcinomaHepatocellular carcinoma recurrence

Identifiers

PMID40844681
PMCPMC12480317

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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.