Direct-acting antiviral agents in the treatment of chronic Hepatitis C – “Real-life” experience from an academic centre and two specialized clinical practices

2017 ◽  
Vol 56 (04) ◽  
pp. 351-360 ◽  
Author(s):  
Manuel Groß ◽  
Georg Härter ◽  
Johanna Backhus ◽  
Eugen Zizer ◽  
Thomas Seufferlein ◽  
...  

AbstractThe introduction of the new direct antiviral agents has revolutionized the therapy of chronic hepatitis C. Today we are able to cure the vast majority of our patients with an 8- to 12-week therapy course of an antiviral combination therapy with an excellent safety profile. Real-life data are very important to further develop our experience with the new therapeutics and help us to improve the care of our patients in our everyday clinical practice.In our study, we present the retrospective analysis of a representative German cohort of 344 patients with chronic hepatitis C treated with the new direct antiviral agents. The patients were recruited in an academic center of southern Germany (University Clinic of Ulm, Clinic of Internal Medicine I) and in 2 highly specialized clinical practices in the city center and the near region of Ulm. Within this in-detail characterized study cohort, we analyzed the efficacy and safety of antiviral therapy under real-life conditions.In 322 patients, we could document SVR12 data and found an excellent overall SVR12 rate of 97.8 % across all genotypes. In more detail, we could show comparable SVR12 results of 99 % and 99.2 % in patients with the hepatitis C virus subtypes 1a and 1b of and an excellent SVR12 rate of 93.1 % in genotype 3 patients without liver cirrhosis. Nevertheless, SVR12 rates tend to be lower in patients with the presence of liver cirrhosis, especially in genotype 3 patients with the lowest SVR12 rate in the whole study group of only 80 %. In general, there were no major safety issues except of 1 patient treated with a protease-inhibitor-based regimen who developed a generalized skin reaction and needed hospitalization and premature end of antiviral therapy.In summary, our analysis of this well characterized representative cohort of 344 patients adds more information in the field of real-life experience with the new antiviral therapeutics and could therefore contribute to improve the care of our patients. Together with the existing real-life data, we now can proceed in achieving the aim of viral eradication of hepatitis C virus within our population.

2021 ◽  
Vol 27 (2) ◽  
pp. 42-48
Author(s):  
Ayhan Balkan ◽  
Yasemin Balkan ◽  
Abdullah Emre Yıldırım ◽  
Buğra Tolga Konduk ◽  
Sezgin Barutçu ◽  
...  

2019 ◽  
Author(s):  
Saima Mushtaq ◽  
Atika Mansoor ◽  
Saima Siddiqi ◽  
Amjad Khan ◽  
Sobia Manzoor

Abstract Background: This study aims to evaluate the clinical effectiveness in terms of sustained virological response (SVR), predictors of SVR and safety of available second generation generic direct-acting antivirals in Pakistani chronic Hepatitis C patients.Methods: This is a retrospective study conducted in multiple centers of Pakistan from January 2015 to January 2019. The samples include patients infected with chronic hepatitis C virus, regardless of virus genotype, cirrhosis, or prior treatment. Statistical analysis was performed to compare the effectiveness among the direct-acting antiviral agents (DAAs) based treatments and also to reveal the factors influencing the achievement of SVR.Results: A total of 993 patients were included in the present study, with the majority receiving sofosbuvir with daclatasvir (95%), sofosbuvir with daclatasvir and ribavirin (4%) and sofosbuvir with ribavirin (1%). There were 96% cases of chronic hepatitis, 3% cases compensated cirrhosis and 1% cases of decompensated cirrhosis. Genotype 3 (99.6%) was the most common genotype. Overall SVR after 12 weeks was 98% for all treatment regimens. High SVR12 was observed with sofosbuvir in combination with daclatasvir (98.5%), then sofosbuvir in combination with daclatasvir and ribavirin (90.2%) and sofosbuvir in combination with ribavirin (75%). SVR rates were high in CHC patients (98.2%) as compared to cirrhotic patients (92.1%) and it was high in treatment naive (98.8%) then IFN experienced patients (90.1%). In multivariate binary logistic regression analysis, patients’ education status, treatment strategy, viral load and ALT had statistically significant association with SVR at 12 weeks. No major adverse events occurred which required treatment discontinuation. Conclusion: Generic oral DAAs (sofosbuvir with daclatasvir) achieved higher SVR12 rates and were well tolerated in this large real‐world cohort of genotype 3 infected patients.


2012 ◽  
Vol 15 (7) ◽  
pp. A326 ◽  
Author(s):  
M.P. Kaczor ◽  
D. Pawlik ◽  
R. Wójcik ◽  
M. Rolka ◽  
I. Maniszewska-Weyher ◽  
...  

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