Poor Sustained Virological Response in a Multicenter Real-Life Cohort of Chronic Hepatitis C Patients Treated with Pegylated Interferon and Ribavirin plus Telaprevir or Boceprevir

Background There are limited data analyzing the effectiveness of boceprevir (BOC) or telaprevir (TVR) in combination with pegylated interferon (PEG-IFN) plus ribavirin (RBV) in a real-life patient cohort. Aims In clinical trials, patients with chronic hepatitis C (CHC) treated with BOC or TVR plus P...

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Veröffentlicht in:Digestive diseases and sciences 2015-04, Vol.60 (4), p.1045-1051
Hauptverfasser: Vo, Kevin P., Vutien, Philip, Akiyama, Matthew J., Vu, Vinh D., Ha, Nghiem B., Piotrowski, Joy I., Wantuck, James, Roytman, Marina M., Tsai, Naoky, Cheung, Ramsey, Li, Jiayi, Nguyen, Mindie H.
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Sprache:eng
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Zusammenfassung:Background There are limited data analyzing the effectiveness of boceprevir (BOC) or telaprevir (TVR) in combination with pegylated interferon (PEG-IFN) plus ribavirin (RBV) in a real-life patient cohort. Aims In clinical trials, patients with chronic hepatitis C (CHC) treated with BOC or TVR plus PEG-IFN and RBV achieved sustained virological response (SVR) rates of 70 %. However, it is not clear whether similar results can be realized in routine practice. Our goal is to examine SVR rates of these triple regimens for CHC in a multicenter real-life patient cohort. Methods We retrospectively studied 200 consecutive CHC genotype 1 patients who were initiated on PEG-IFN, RBV, and either TVR ( n  = 113) or BOC ( n  = 87) from July 2011 to February 2014 at two US academic liver clinics, a Veterans Affairs liver clinic and a community gastroenterology clinic. Results Both BOC and TVR treatment groups were similar in regard to comorbidities, BMI, and HCV RNA levels. BOC patients were more likely to have cirrhosis than TVR patients (47 vs. 24 %, P  = 0.001). SVR rates were low in both cohorts (40 % for BOC, 53 % for TVR, P  = 0.05). On multivariate logistic regression, treatment adherence by the “80/80/80 rule,” diagnosis of cirrhosis, and use of erythropoietin were statistically significant predictors for SVR. Of these, treatment adherence was the strongest predictor (OR 4.43, 95 % CI 2.8–6.06, P  
ISSN:0163-2116
1573-2568
DOI:10.1007/s10620-015-3621-0