Digestive Diseases and Sciences

, Volume 60, Issue 4, pp 1045–1051 | Cite as

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

  • Kevin P. Vo
  • Philip Vutien
  • Matthew J. Akiyama
  • Vinh D. Vu
  • Nghiem B. Ha
  • Joy I. Piotrowski
  • James Wantuck
  • Marina M. Roytman
  • Naoky Tsai
  • Ramsey Cheung
  • Jiayi Li
  • Mindie H. Nguyen
Original Article



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.


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.


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.


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 < 0.001).


SVR was much lower in a real-life patient cohort than in clinical trials (53 % for TVR and 40 % for BOC, compared to 66–75 % in clinical trials).


HCV Routine practice Effectiveness PEG-IFN TVR BOC 



Hepatitis C virus


Sustained virological response


Pegylated interferon and ribavirin


Randomized controlled trial




Early virological response


Conflict of interest

Kevin P. Vo, Philip Vutien, Matthew J. Akiyama, Vinh D. Vu, Nghiem B. Ha, Joy I. Piotrowski, and James Wantuck have none to declare. Marina M. Roytman is on Gilead speakers’ bureau and advisory board. Naoky Tsai discloses research grants with AbbVie, Janssen, Gilead Sciences, BMS, and Beckman. Naoky Tsai discloses he is on the Speaker’s bureau for AbbVie, Janssen, Gilead Sciences, BMS, Salix, and Bayer, and is also on the advisory board for Gilead Sciences and AbbVie. Ramsey Cheung discloses research grants with Gilead Sciences. Jiayi Li discloses he is a speaker for Gilead Sciences. Mindie H. Nguyen discloses she has received honoraria and research support from Bristol-Myers Squibb, Gilead Sciences, and Janssen Pharmaceuticals.


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Copyright information

© Springer Science+Business Media New York 2015

Authors and Affiliations

  • Kevin P. Vo
    • 1
  • Philip Vutien
    • 1
  • Matthew J. Akiyama
    • 5
  • Vinh D. Vu
    • 1
  • Nghiem B. Ha
    • 1
  • Joy I. Piotrowski
    • 2
  • James Wantuck
    • 1
  • Marina M. Roytman
    • 2
  • Naoky Tsai
    • 2
  • Ramsey Cheung
    • 3
  • Jiayi Li
    • 4
  • Mindie H. Nguyen
    • 1
  1. 1.Division of Gastroenterology and HepatologyStanford University Medical CenterPalo AltoUSA
  2. 2.The Queens Medical CenterUniversity of HawaiiHonoluluUSA
  3. 3.VA Palo AltoPalo AltoUSA
  4. 4.Palo Alto Medical Foundation Camino DivisionMountain ViewUSA
  5. 5.Division of Infectious DiseasesNew York University School of MedicineNew YorkUSA

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