Cargando…

Antiviral therapy for prevention of hepatocellular carcinoma and mortality in chronic hepatitis B: systematic review and meta-analysis

OBJECTIVES: The effect of antiviral therapy on clinical outcomes in chronic hepatitis B virus (HBV) is not established. We aimed to assess the effects of interferon and/or nucleos(t)ide analogues versus placebo or no intervention on prevention of hepatocellular carcinoma (HCC) and mortality in chron...

Descripción completa

Detalles Bibliográficos
Autores principales: Thiele, Maja, Gluud, Lise L, Dahl, Emilie K, Krag, Aleksander
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3752055/
https://www.ncbi.nlm.nih.gov/pubmed/23945731
http://dx.doi.org/10.1136/bmjopen-2013-003265
_version_ 1782281721452953600
author Thiele, Maja
Gluud, Lise L
Dahl, Emilie K
Krag, Aleksander
author_facet Thiele, Maja
Gluud, Lise L
Dahl, Emilie K
Krag, Aleksander
author_sort Thiele, Maja
collection PubMed
description OBJECTIVES: The effect of antiviral therapy on clinical outcomes in chronic hepatitis B virus (HBV) is not established. We aimed to assess the effects of interferon and/or nucleos(t)ide analogues versus placebo or no intervention on prevention of hepatocellular carcinoma (HCC) and mortality in chronic HBV. DESIGN: Random-effects pairwise meta-analysis of randomised trials and observational studies. SETTING: Electronic and manual searches were combined. Randomised controlled trials (RCTs) were included in the primary analyses. Observational studies were included in sensitivity analyses. PRIMARY AND SECONDARY OUTCOME MEASURES: The primary outcome measures were HCC incidence and mortality. The secondary outcome measure was HCC mortality. RESULTS: We included 8 RCTs, 8 prospective cohort studies and 19 case–control studies with a total of 3433 patients allocated to antiviral therapy and 4625 controls. The maximum duration of follow-up was 23 years. Randomised trials found no effect of antiviral therapy on HCC or mortality. Cohort studies found that antiviral therapy increased the risk of HCC (risk ratio 1.43; 95% CI 1.06 to 1.95), whereas case–control studies found a decreased risk of HCC in the intervention group (risk ratio 0.69; 95% CI 0.54 to 0.88). There was a clear difference between the results of RCTs and observational studies (test for subgroup differences, p<0.001). Antiviral therapy did not affect mortality in cohort studies, but reduced mortality in case–control studies (relative risk 0.71; 95% CI 0.54 to 0.93; test for subgroup differences, p=0.406). CONCLUSIONS: The effect of antiviral therapy on clinical outcomes in HBV remains to be established. Although there was a positive effect in the sensitivity analyses, the strength of the evidence does not allow for extrapolation to clinical practice as research design plays an essential role in the overall assessment. TRIAL REGISTRATION NUMBER: Prospero number CRD42013003881.
format Online
Article
Text
id pubmed-3752055
institution National Center for Biotechnology Information
language English
publishDate 2013
publisher BMJ Publishing Group
record_format MEDLINE/PubMed
spelling pubmed-37520552013-08-27 Antiviral therapy for prevention of hepatocellular carcinoma and mortality in chronic hepatitis B: systematic review and meta-analysis Thiele, Maja Gluud, Lise L Dahl, Emilie K Krag, Aleksander BMJ Open Gastroenterology and Hepatology OBJECTIVES: The effect of antiviral therapy on clinical outcomes in chronic hepatitis B virus (HBV) is not established. We aimed to assess the effects of interferon and/or nucleos(t)ide analogues versus placebo or no intervention on prevention of hepatocellular carcinoma (HCC) and mortality in chronic HBV. DESIGN: Random-effects pairwise meta-analysis of randomised trials and observational studies. SETTING: Electronic and manual searches were combined. Randomised controlled trials (RCTs) were included in the primary analyses. Observational studies were included in sensitivity analyses. PRIMARY AND SECONDARY OUTCOME MEASURES: The primary outcome measures were HCC incidence and mortality. The secondary outcome measure was HCC mortality. RESULTS: We included 8 RCTs, 8 prospective cohort studies and 19 case–control studies with a total of 3433 patients allocated to antiviral therapy and 4625 controls. The maximum duration of follow-up was 23 years. Randomised trials found no effect of antiviral therapy on HCC or mortality. Cohort studies found that antiviral therapy increased the risk of HCC (risk ratio 1.43; 95% CI 1.06 to 1.95), whereas case–control studies found a decreased risk of HCC in the intervention group (risk ratio 0.69; 95% CI 0.54 to 0.88). There was a clear difference between the results of RCTs and observational studies (test for subgroup differences, p<0.001). Antiviral therapy did not affect mortality in cohort studies, but reduced mortality in case–control studies (relative risk 0.71; 95% CI 0.54 to 0.93; test for subgroup differences, p=0.406). CONCLUSIONS: The effect of antiviral therapy on clinical outcomes in HBV remains to be established. Although there was a positive effect in the sensitivity analyses, the strength of the evidence does not allow for extrapolation to clinical practice as research design plays an essential role in the overall assessment. TRIAL REGISTRATION NUMBER: Prospero number CRD42013003881. BMJ Publishing Group 2013-08-13 /pmc/articles/PMC3752055/ /pubmed/23945731 http://dx.doi.org/10.1136/bmjopen-2013-003265 Text en Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions This is an Open Access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 3.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Gastroenterology and Hepatology
Thiele, Maja
Gluud, Lise L
Dahl, Emilie K
Krag, Aleksander
Antiviral therapy for prevention of hepatocellular carcinoma and mortality in chronic hepatitis B: systematic review and meta-analysis
title Antiviral therapy for prevention of hepatocellular carcinoma and mortality in chronic hepatitis B: systematic review and meta-analysis
title_full Antiviral therapy for prevention of hepatocellular carcinoma and mortality in chronic hepatitis B: systematic review and meta-analysis
title_fullStr Antiviral therapy for prevention of hepatocellular carcinoma and mortality in chronic hepatitis B: systematic review and meta-analysis
title_full_unstemmed Antiviral therapy for prevention of hepatocellular carcinoma and mortality in chronic hepatitis B: systematic review and meta-analysis
title_short Antiviral therapy for prevention of hepatocellular carcinoma and mortality in chronic hepatitis B: systematic review and meta-analysis
title_sort antiviral therapy for prevention of hepatocellular carcinoma and mortality in chronic hepatitis b: systematic review and meta-analysis
topic Gastroenterology and Hepatology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3752055/
https://www.ncbi.nlm.nih.gov/pubmed/23945731
http://dx.doi.org/10.1136/bmjopen-2013-003265
work_keys_str_mv AT thielemaja antiviraltherapyforpreventionofhepatocellularcarcinomaandmortalityinchronichepatitisbsystematicreviewandmetaanalysis
AT gluudlisel antiviraltherapyforpreventionofhepatocellularcarcinomaandmortalityinchronichepatitisbsystematicreviewandmetaanalysis
AT dahlemiliek antiviraltherapyforpreventionofhepatocellularcarcinomaandmortalityinchronichepatitisbsystematicreviewandmetaanalysis
AT kragaleksander antiviraltherapyforpreventionofhepatocellularcarcinomaandmortalityinchronichepatitisbsystematicreviewandmetaanalysis