Real-World Effectiveness of Direct-Acting Antiviral Regimens against Hepatitis C Virus (HCV) Genotype 3 Infection: A Systematic Review and Meta-Analysis.
Ann Hepatol
; 23: 100268, 2021.
Article
en En
| MEDLINE
| ID: mdl-33059055
ABSTRACT
Patients with hepatitis C virus (HCV) genotype 3 (GT3) infection are resistant to direct-acting antiviral (DAA) treatments. This study aimed to analyze the effectiveness of sofosbuvir (SOF)+daclatasvir (DCV) ± ribavirin (RBV); SOF+velpatasvir (VEL)±RBV; SOF+VEL+voxilaprevir (VOX); and glecaprevir (GLE)+pibrentasvir (PIB) in the treatment of HCV GT3-infected patients in real-world studies. Articles were identified by searching the PubMed, EMBASE, and Cochrane Library databases from January 1, 2016 to September 10, 2019. The meta-analysis was conducted to determine the sustained virologic response (SVR) rate, using R 3.6.2 software. Thirty-four studies, conducted on a total of 7328 patients from 22 countries, met the inclusion criteria. The pooled SVR rate after 12/24 weeks of treatment was 92.07% (95% CI 90.39-93.61%) for the evaluated regimens. Also, the SVR rate was 91.17% (95% CI 89.23-92.94%) in patients treated with SOF+DCV±RBV; 95.08% (95% CI 90.88-98.13%) in patients treated with SOF+VEL±RBV; 84.97% (95% CI 73.32-93.91%) in patients treated with SOF+VEL+VOX; and 98.54% (95% CI 96.40-99.82%) in patients treated with GLE+PIB. The pooled SVR rate of the four regimens was 95.24% (95% CI 93.50-96.75%) in non-cirrhotic patients and 89.39% (95% CI 86.07-92.33%) in cirrhotic patients. The pooled SVR rate was 94.41% (95% CI 92.02-96.42%) in treatment-naive patients and 87.98% (95% CI 84.31-91.25%) in treatment-experienced patients. The SVR rate of GLE+PIB was higher than other regimens. SOF+VEL+VOX can be used as a treatment regimen following DAA treatment failure.
Palabras clave
Texto completo:
1
Banco de datos:
MEDLINE
Asunto principal:
Antivirales
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Pirrolidinas
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Quinoxalinas
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Sulfonamidas
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Valina
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Bencimidazoles
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Carbamatos
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Hepatitis C
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Compuestos Macrocíclicos
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Sofosbuvir
Tipo de estudio:
Prognostic_studies
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Systematic_reviews
Límite:
Humans
Idioma:
En
Año:
2021
Tipo del documento:
Article