Sustained virologic response to direct-acting antiviral therapy in patients with chronic hepatitis C and hepatocellular carcinoma: A systematic review and meta-analysis.
2-Naphthylamine
Adolescent
Adult
Anilides
/ therapeutic use
Antiviral Agents
/ therapeutic use
Benzimidazoles
/ therapeutic use
Carbamates
/ therapeutic use
Carcinoma, Hepatocellular
/ complications
Cyclopropanes
Female
Fluorenes
/ therapeutic use
Hepacivirus
/ drug effects
Hepatitis C, Chronic
/ complications
Humans
Isoquinolines
/ therapeutic use
Lactams, Macrocyclic
Liver Neoplasms
/ complications
Liver Transplantation
Macrocyclic Compounds
/ therapeutic use
Male
Proline
/ analogs & derivatives
Ritonavir
/ therapeutic use
Sofosbuvir
/ therapeutic use
Sulfonamides
/ therapeutic use
Sustained Virologic Response
Uracil
/ analogs & derivatives
Valine
Young Adult
Asian
HCC treatment
Liver transplant
Non-Asian
Real-world analysis
Journal
Journal of hepatology
ISSN: 1600-0641
Titre abrégé: J Hepatol
Pays: Netherlands
ID NLM: 8503886
Informations de publication
Date de publication:
09 2019
09 2019
Historique:
received:
23
07
2018
revised:
31
03
2019
accepted:
25
04
2019
pubmed:
17
5
2019
medline:
15
12
2020
entrez:
17
5
2019
Statut:
ppublish
Résumé
The effect of hepatocellular carcinoma (HCC) on the response to interferon-free direct-acting antiviral (DAA) therapy in patients with chronic hepatitis C (CHC) infection remains unclear. Using a systematic review and meta-analysis approach, we aimed to investigate the effect of DAA therapy on sustained virologic response (SVR) among patients with CHC and either active, inactive or no HCC. PubMed, Embase, Web of Science, and the Cochrane Central Register of Controlled Trials were searched from 1/1/2013 to 9/24/2018. The pooled SVR rates were computed using DerSimonian-Laird random-effects models. We included 49 studies from 15 countries, comprised of 3,341 patients with HCC and 35,701 without HCC. Overall, the pooled SVR was lower in patients with HCC than in those without HCC (89.6%, 95% CI 86.8-92.1%, I Overall, SVR rates were lower in patients with HCC, especially with active HCC, compared to those without HCC, though heterogeneity was high. Continued efforts are needed to aggressively screen, diagnose, and treat HCC to ensure higher CHC cure rates. There are now medications (direct-acting antivirals or "DAAs") that can "cure" hepatitis C virus, but patients with hepatitis C and liver cancer may be less likely to achieve cure than those without liver cancer. However, patients with liver cancer are also more likely to have advanced liver disease and risk factors that can decrease cure rates, so better controlled studies are needed to confirm these findings.
Sections du résumé
BACKGROUND & AIMS
The effect of hepatocellular carcinoma (HCC) on the response to interferon-free direct-acting antiviral (DAA) therapy in patients with chronic hepatitis C (CHC) infection remains unclear. Using a systematic review and meta-analysis approach, we aimed to investigate the effect of DAA therapy on sustained virologic response (SVR) among patients with CHC and either active, inactive or no HCC.
METHODS
PubMed, Embase, Web of Science, and the Cochrane Central Register of Controlled Trials were searched from 1/1/2013 to 9/24/2018. The pooled SVR rates were computed using DerSimonian-Laird random-effects models.
RESULTS
We included 49 studies from 15 countries, comprised of 3,341 patients with HCC and 35,701 without HCC. Overall, the pooled SVR was lower in patients with HCC than in those without HCC (89.6%, 95% CI 86.8-92.1%, I
CONCLUSION
Overall, SVR rates were lower in patients with HCC, especially with active HCC, compared to those without HCC, though heterogeneity was high. Continued efforts are needed to aggressively screen, diagnose, and treat HCC to ensure higher CHC cure rates.
LAY SUMMARY
There are now medications (direct-acting antivirals or "DAAs") that can "cure" hepatitis C virus, but patients with hepatitis C and liver cancer may be less likely to achieve cure than those without liver cancer. However, patients with liver cancer are also more likely to have advanced liver disease and risk factors that can decrease cure rates, so better controlled studies are needed to confirm these findings.
Identifiants
pubmed: 31096005
pii: S0168-8278(19)30279-X
doi: 10.1016/j.jhep.2019.04.017
pii:
doi:
Substances chimiques
Anilides
0
Antiviral Agents
0
Benzimidazoles
0
Carbamates
0
Cyclopropanes
0
Fluorenes
0
Isoquinolines
0
Lactams, Macrocyclic
0
Macrocyclic Compounds
0
Sulfonamides
0
ledipasvir, sofosbuvir drug combination
0
ombitasvir
2302768XJ8
Uracil
56HH86ZVCT
Proline
9DLQ4CIU6V
2-Naphthylamine
CKR7XL41N4
dasabuvir
DE54EQW8T1
Valine
HG18B9YRS7
Ritonavir
O3J8G9O825
paritaprevir
OU2YM37K86
asunaprevir
S9X0KRJ00S
Sofosbuvir
WJ6CA3ZU8B
Types de publication
Journal Article
Meta-Analysis
Systematic Review
Langues
eng
Sous-ensembles de citation
IM
Pagination
473-485Informations de copyright
Copyright © 2019 European Association for the Study of the Liver. Published by Elsevier B.V. All rights reserved.