Efficacy, Safety, and Predictors of Direct-acting antivirals in Hepatitis C Virus Patients with Heterogeneous Liver Diseases

被引:0
|
作者
De Pace, Vanessa [1 ]
Morelli, Maria Cristina [1 ]
Ravaioli, Matteo [1 ]
Maggi, Fabrizio [2 ,3 ,4 ]
Galli, Silvia [5 ,6 ]
Vero, Vittoria [6 ,7 ]
Re, Maria Carla [5 ,6 ]
Cescon, Matteo [1 ]
Pistello, Mauro [2 ,3 ,4 ]
机构
[1] Univ Bologna, St Orsola Malpighi Hosp, Dept Med & Surg Sci, Gen & Transplant Surg Unit, Bologna, Italy
[2] Univ Pisa, Pisa Univ Hosp, Virol Unit, Pisa, Italy
[3] Univ Pisa, Virol Sect, Pisa, Italy
[4] Univ Pisa, Retrovirus Ctr, Pisa, Italy
[5] Univ Bologna, Dept Expt Diagnost & Specialty Med, Microbiol & Virol Unit, Bologna, Italy
[6] St Orsola Malpighi Hosp, Bologna, Italy
[7] Univ Bologna, Dept Med & Surg Sci, End Stage Liver Dis Unit, Bologna, Italy
来源
NEW MICROBIOLOGICA | 2019年 / 42卷 / 04期
关键词
Hepatitis C Virus (HCV); anti-HCV Direct-Acting Antivirals (DAA); combination therapy; viral resistance; SIMEPREVIR PLUS SOFOSBUVIR; ALPHA-FETOPROTEIN; INFECTION; RIBAVIRIN; CIRRHOSIS; ABT-450/R-OMBITASVIR; LEDIPASVIR; DASABUVIR; REGIMENS; PHASE-3;
D O I
暂无
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Safety, efficacy, and predictor factors of sustained-virological-response after 24 weeks of new direct-acting antivirals were evaluated in hepatitis C virus patients with different stages of hepatic disease. 260 patients, median age 60 years, of whom 48.1% cirrhotics, 17.7% liver transplant recipients, and 45.7% naive were treated with Sofosbuvir +/- Ribavirine, Sofosbuvir+Simeprevir +/- Ribavirine, Sofosbuvir+Daclatasvir +/- Ribavirine, Sofosbuvir+Ledispavir +/- Ribavirine, Ombitasvir/Paritaprevir/Ritonavir+Ribavirine and Ombitanir/Paritaprevir/Ritonavir+Dasabuvir +/- Ribavirine. Therapy outcomes, hematochemical parameters, viral replication, genotype, and resistance-associated-mutations were analyzed retrospectively. Sustained virological response was 90.4% in the whole population, 83.2% in cirrhotics, 85% in patients with previous virological failure, 93.6 degrees k in patients >60 years, and 95.6% in liver transplant recipients. SVR24 for each drug regimen was 75% Sofosbuvir+Ribavirine, 80.4% Sofosbuvir+Simeprevir +/- Ribavirine, 94.3% Sofosbuvir+Daclatasvir +/- Ribavirine, 98.7% Sofosbuvir+Ledispavir +/- Ribavirine, 100% Ombitasvir/ Paritaprevir/Ritonavir+Ribavirine and Ombitasvir/Paritaprevir/Ritonavir+Dasabuvir +/- Ribavirine. The highest sustained virological response rates were obtained with genotype-1b (95.9%). Twenty-five patients, mostly cirrhotics or suffering from severe liver complications, manifested relapse (84%), breakthrough (12%), or non-response (4%). Mild side effects were observed in 41.1% of patients. Model-for-End-Liver-Disease score <10 and alanine aminotransferase <= 20 U/L at week 8 of therapy proved positive predictors of sustained virological response. Direct-acting antiviral therapy is efficacious and safe even in patients with advanced liver disease and/or previous virological failure; Model-for-End-Liver-Disease <10 and alanine aminotransferase reduction during therapy were found to be reliable predicting markers of sustained-virological-response.
引用
收藏
页码:189 / 196
页数:8
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