Evidence map›Paper›PMID 22537438›Full record

ReviewGastroenterology2012

Maximizing opportunities and avoiding mistakes in triple therapy for hepatitis C virus.

A Sidney Barritt, Michael W Fried

Registry-linked trialOpen access · bronzeAbstract readReview
In one paragraph

Review in Gastroenterology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT01831037 (The Regression of Liver Fibrosis and Risk for Hepatocellular Carcinoma), which is not on this map. Cited by 25 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed, 1 pooled it
6.8field-weighted citation impact, top 2% of its field
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.

NCT01831037 withdrawnnot on this mapstarted 2015, after this paper: background citation

The Regression of Liver Fibrosis and Risk for Hepatocellular Carcinoma (ROLFH) Study

TypeobservationalSponsorUniversity of ArkansasRan2015 to 2019Enrolled0ConditionsChronic Hepatitis C, Chronic Hepatitis BArmsRegression of fibrosis, Specific risk factors related to hepatocellular carcinoma
3 · Its place in the literature

Who cites it

25 citing papers in PubMed, 1 synthesis or guideline pooled it, 59 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Article
  4. Review
  5. Review
  6. Review
  7. Article
  8. Review
  9. Article
  10. Observational
  11. Observational
  12. Article
  13. Review
  14. Clinical liver disease · 2015
    Review
  15. Management of viral hepatitis in liver transplant recipients.Clinical and molecular hepatology · 2014
    Review
  16. Review
  17. Observational
  18. Review
  19. Review
  20. Review
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

2 authors at 1 institution in 1 country.

A Sidney BarrittUniversity of North Carolina at Chapel Hill, UNC Liver Center, Division of Gastroenterology and Hepatology, Chapel Hill, North Carolina 27599-7584, USA. barritt@med.unc.edu
Michael W Fried
University of North Carolina at Chapel Hill · US

Funding

UNC Clinical Translation Science Award-K12 Scholars Program (KL2)KL2RR025746 · NCRR · UNIV OF NORTH CAROLINA CHAPEL HILL · PI RUNGE, MARSCHALL S. · 2008 to 2011
$9.0M
Mentoring Junior Faculty: Viral hepatitis Clinical ResearchK24DK066144 · NIDDK · UNIV OF NORTH CAROLINA CHAPEL HILL · PI FRIED, MICHAEL W · 2004 to 2014
$1.5M
NCRR NIH HHS 1KL2-RR025746-03NCRR NIH HHS KL2 RR025746NIDDK NIH HHS K24 DK066144
6 · The paper itself

Abstract

Recently developed drugs and innovative strategies for the treatment of chronic infection with genotype 1 hepatitis C virus (HCV) have become the standard of care. The protease inhibitors telaprevir (Incivek) and boceprevir (Victrelis) are the first direct-acting antiviral (DAA) agents approved, and many more are being developed. These drugs substantially increased rates of sustained virologic response in treatment-naïve and -experienced patients, in conjunction with peginterferon and ribavirin (triple therapy), in phase 3 trials. The efficacy of triple therapy depends on appropriate selection of patients, although the population of patients that receive triple therapy could be expanded as the risk/benefit ratio improves. Attention to details that reflect the standard of care, such as appropriate dosing, anticipation of adverse effects, and strict adherence to stopping rules, will insure the success of these drugs and lead the way for new combination therapies.

Indexed as

Anemia, HypochromicAntiviral AgentsClinical Trials as TopicDrug Administration ScheduleDrug EruptionsDrug InteractionsDrug Therapy, CombinationGastrointestinal TractHepacivirusHepatitis C, ChronicHumansInterferon-alphaOligopeptidesPolyethylene GlycolsProlineRecombinant ProteinsAntiviral AgentsInterferon-alphaN-(3-amino-1-(cyclobutylmethyl)-2,3-dioxopropyl)-3-(2-((((1,1-dimethylethyl)amino)carbonyl)amino)-3,3-dimethyl-1-oxobutyl)-6,6-dimethyl-3-azabicyclo(3.1.0)hexan-2-carboxamideOligopeptidespeginterferon alfa-2aPolyethylene GlycolsProlineRecombinant ProteinsRibavirinSerine Proteinase Inhibitorstelaprevir

Identifiers

PMID22537438
PMCPMC3683992
OpenAlexW2035035323

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

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.