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Satisfactory virological response and fibrosis improvement of sofosbuvir-based regimens for Chinese patients with hepatitis C virus genotype 3 infection: results of a real-world cohort study
by
Deng, Rong
, Wang, Yong-Hong
, Wang, Meng-Lan
, Lv, Duo-Duo
, Yuan, Man
, Chen, En-Qiang
, Tang, Hong
, Tao, Ya-Chao
in
Adult
/ Antiviral agents
/ Antiviral Agents - therapeutic use
/ Antiviral drugs
/ Asian People
/ Benzimidazoles
/ Benzopyrans
/ Biomedical and Life Sciences
/ Biomedicine
/ Carbamates - therapeutic use
/ Chronic hepatitis C
/ Chronic infection
/ Cirrhosis
/ Cohort analysis
/ cohort studies
/ Complications and side effects
/ Direct-acting antivirals
/ Dosage and administration
/ Drug dosages
/ Drug therapy
/ FDA approval
/ Female
/ Fibrosis
/ Follow-Up Studies
/ Genotype
/ Genotype & phenotype
/ Genotype 3
/ Genotypes
/ Hepacivirus - classification
/ Hepacivirus - isolation & purification
/ Hepatitis
/ Hepatitis C
/ Hepatitis C virus
/ Hepatitis C, Chronic - complications
/ Hepatitis C, Chronic - drug therapy
/ Hepatitis C, Chronic - virology
/ Hepatitis viruses
/ Hepatology
/ Heterocyclic Compounds, 4 or More Rings - therapeutic use
/ Humans
/ Imidazoles - therapeutic use
/ Infections
/ Interferon
/ Liver cirrhosis
/ Liver Cirrhosis - pathology
/ Liver diseases
/ Male
/ Middle Aged
/ Patients
/ Pharmacy
/ Pyrrolidines
/ Remission
/ Retrospective Studies
/ Ribavirin
/ Ribavirin - therapeutic use
/ Sofosbuvir
/ Sofosbuvir - therapeutic use
/ Sofosbuvir-based regimens
/ Sustained Virologic Response
/ therapeutics
/ Treatment Outcome
/ Valine - analogs & derivatives
/ Virology
2018
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Satisfactory virological response and fibrosis improvement of sofosbuvir-based regimens for Chinese patients with hepatitis C virus genotype 3 infection: results of a real-world cohort study
by
Deng, Rong
, Wang, Yong-Hong
, Wang, Meng-Lan
, Lv, Duo-Duo
, Yuan, Man
, Chen, En-Qiang
, Tang, Hong
, Tao, Ya-Chao
in
Adult
/ Antiviral agents
/ Antiviral Agents - therapeutic use
/ Antiviral drugs
/ Asian People
/ Benzimidazoles
/ Benzopyrans
/ Biomedical and Life Sciences
/ Biomedicine
/ Carbamates - therapeutic use
/ Chronic hepatitis C
/ Chronic infection
/ Cirrhosis
/ Cohort analysis
/ cohort studies
/ Complications and side effects
/ Direct-acting antivirals
/ Dosage and administration
/ Drug dosages
/ Drug therapy
/ FDA approval
/ Female
/ Fibrosis
/ Follow-Up Studies
/ Genotype
/ Genotype & phenotype
/ Genotype 3
/ Genotypes
/ Hepacivirus - classification
/ Hepacivirus - isolation & purification
/ Hepatitis
/ Hepatitis C
/ Hepatitis C virus
/ Hepatitis C, Chronic - complications
/ Hepatitis C, Chronic - drug therapy
/ Hepatitis C, Chronic - virology
/ Hepatitis viruses
/ Hepatology
/ Heterocyclic Compounds, 4 or More Rings - therapeutic use
/ Humans
/ Imidazoles - therapeutic use
/ Infections
/ Interferon
/ Liver cirrhosis
/ Liver Cirrhosis - pathology
/ Liver diseases
/ Male
/ Middle Aged
/ Patients
/ Pharmacy
/ Pyrrolidines
/ Remission
/ Retrospective Studies
/ Ribavirin
/ Ribavirin - therapeutic use
/ Sofosbuvir
/ Sofosbuvir - therapeutic use
/ Sofosbuvir-based regimens
/ Sustained Virologic Response
/ therapeutics
/ Treatment Outcome
/ Valine - analogs & derivatives
/ Virology
2018
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Satisfactory virological response and fibrosis improvement of sofosbuvir-based regimens for Chinese patients with hepatitis C virus genotype 3 infection: results of a real-world cohort study
by
Deng, Rong
, Wang, Yong-Hong
, Wang, Meng-Lan
, Lv, Duo-Duo
, Yuan, Man
, Chen, En-Qiang
, Tang, Hong
, Tao, Ya-Chao
in
Adult
/ Antiviral agents
/ Antiviral Agents - therapeutic use
/ Antiviral drugs
/ Asian People
/ Benzimidazoles
/ Benzopyrans
/ Biomedical and Life Sciences
/ Biomedicine
/ Carbamates - therapeutic use
/ Chronic hepatitis C
/ Chronic infection
/ Cirrhosis
/ Cohort analysis
/ cohort studies
/ Complications and side effects
/ Direct-acting antivirals
/ Dosage and administration
/ Drug dosages
/ Drug therapy
/ FDA approval
/ Female
/ Fibrosis
/ Follow-Up Studies
/ Genotype
/ Genotype & phenotype
/ Genotype 3
/ Genotypes
/ Hepacivirus - classification
/ Hepacivirus - isolation & purification
/ Hepatitis
/ Hepatitis C
/ Hepatitis C virus
/ Hepatitis C, Chronic - complications
/ Hepatitis C, Chronic - drug therapy
/ Hepatitis C, Chronic - virology
/ Hepatitis viruses
/ Hepatology
/ Heterocyclic Compounds, 4 or More Rings - therapeutic use
/ Humans
/ Imidazoles - therapeutic use
/ Infections
/ Interferon
/ Liver cirrhosis
/ Liver Cirrhosis - pathology
/ Liver diseases
/ Male
/ Middle Aged
/ Patients
/ Pharmacy
/ Pyrrolidines
/ Remission
/ Retrospective Studies
/ Ribavirin
/ Ribavirin - therapeutic use
/ Sofosbuvir
/ Sofosbuvir - therapeutic use
/ Sofosbuvir-based regimens
/ Sustained Virologic Response
/ therapeutics
/ Treatment Outcome
/ Valine - analogs & derivatives
/ Virology
2018
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Satisfactory virological response and fibrosis improvement of sofosbuvir-based regimens for Chinese patients with hepatitis C virus genotype 3 infection: results of a real-world cohort study
Journal Article
Satisfactory virological response and fibrosis improvement of sofosbuvir-based regimens for Chinese patients with hepatitis C virus genotype 3 infection: results of a real-world cohort study
2018
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Overview
Background
Chronic hepatitis C virus (HCV) genotype (GT) 3 infection with advanced liver disease has emerged as a challenging to treat by direct-acting antivirals (DAAs), but the efficacy of DAAs in Chinese HCV-GT3 patients is rarely reported. This study aimed to analyze the efficacy of sofosbuvir (SOF)-based regimens in Chinese patients with HCV-GT3 and compensated liver disease.
Methods
This was a registered retrospective study. All patients had completed at least 12 weeks SOF-based regimens therapy (with or without RBV), and were followed up for at least 24 weeks after therapy discontinuation. The primary endpoint was sustained virological response 24 weeks after end of therapy (SVR24).
Results
A total of 102 patients who completed at least 12 weeks therapy were finally included, with 57 in SOF + Daclatasvir (SOF + DCV), 24 in SOF + DCV + ribavirin (RBV) and 21 in SOF/Velpatasvir (SOF/VEL). The total SVR24 rate was achieved in 90.20% (92/102), with 85.96% (49/57) in SOF + DCV, 91.67% (22/24) in SOF + DCV + RBV and 100.00% (21/21) in SOF/VEL. Among 10 relapsed patients (8 in SOF + DCV and 2 in SOF + DCV + RBV), the short course (12 weeks) of therapy and no RBV addition may be the leading cause. In this cohort, the SVR24 rate was not statistically different between patients with and without cirrhosis (81.82% [27/33] vs. 94.20% [65/69],
P
= 0.073). Additionally, both FIB-4 (4.03 vs. 2.08,
P
< 0.001) and APRI (2.15 vs. 0.68,
P
< 0.001) scores were significant improved from baseline to week 24 after completion of therapy, regardless of the presence of cirrhosis.
Conclusion
SOF-based regimens are highly effective in viral clearance and fibrosis remission for Chinese patients with HCV-GT3 infection. If available, SOF/VEL should be first considered.
Publisher
BioMed Central,BioMed Central Ltd,Springer Nature B.V,BMC
Subject
/ Antiviral Agents - therapeutic use
/ Biomedical and Life Sciences
/ Carbamates - therapeutic use
/ Complications and side effects
/ Female
/ Fibrosis
/ Genotype
/ Hepacivirus - classification
/ Hepacivirus - isolation & purification
/ Hepatitis C, Chronic - complications
/ Hepatitis C, Chronic - drug therapy
/ Hepatitis C, Chronic - virology
/ Heterocyclic Compounds, 4 or More Rings - therapeutic use
/ Humans
/ Imidazoles - therapeutic use
/ Male
/ Patients
/ Pharmacy
/ Sofosbuvir - therapeutic use
/ Sustained Virologic Response
/ Valine - analogs & derivatives
/ Virology
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