Unknown

Dataset Information

0

Efficacy and safety of danoprevir-ritonavir plus peginterferon alfa-2a-ribavirin in hepatitis C virus genotype 1 prior null responders.


ABSTRACT: Danoprevir (DNV) is a hepatitis C virus (HCV) protease inhibitor that achieves high sustained virologic response (SVR) rates in combination with peginterferon alfa-2a-ribavirin in treatment-naive HCV genotype 1 (G1)-infected patients. This study explored the efficacy and safety of ritonavir-boosted DNV (DNVr) plus peginterferon alfa-2a-ribavirin in G1-infected prior peginterferon-ribavirin null responders. Null responders (<2-log10 reduction in HCV RNA level at week 12) were given an open-label combination of 100 mg of ritonavir and 100 mg of DNV (100/100 mg DNVr) every 12 h (q12h) plus peginterferon alfa-2a-ribavirin for 12 weeks. All patients achieving an early virologic response (EVR; ?2-log10 decrease in HCV RNA by week 12) continued treatment with peginterferon alfa-2a-ribavirin; those without an EVR discontinued all study drugs. Twenty-four prior null responders were enrolled; 16 patients (67%) were infected with HCV G1b, and 8 (33%) were infected with G1a. Ninety-six percent of patients had an IL28B non-CC genotype. A sustained virologic response at 24 weeks posttreatment (SVR24) was achieved in 67% of patients, with a higher rate in G1b-infected (88%) than G1a-infected (25%) patients. Resistance-related breakthrough occurred in 4/8 G1a and 1/16 G1b patients through the DNV resistance-associated variant (RAV) NS3 R155K. NS3 R155K was also detected in 2/2 G1a patients who relapsed. Treatment was well tolerated. Two patients withdrew prematurely from study medications due to adverse events. Two serious adverse events were reported; both occurred after completion of DNVr therapy and were considered unrelated to treatment. No grade 3 or 4 alanine aminotransferase (ALT) elevations were observed. DNVr plus peginterferon alfa-2a-ribavirin demonstrated high SVR24 rates in HCV G1b-infected prior null responders and was well tolerated. (This study has been registered at ClinicalTrials.gov under registration no. NCT01185860.).

SUBMITTER: Gane EJ 

PROVIDER: S-EPMC3910820 | biostudies-literature | 2014

REPOSITORIES: biostudies-literature

altmetric image

Publications

Efficacy and safety of danoprevir-ritonavir plus peginterferon alfa-2a-ribavirin in hepatitis C virus genotype 1 prior null responders.

Gane Edward J EJ   Rouzier Régine R   Wiercinska-Drapalo Alicja A   Larrey Dominique G DG   Morcos Peter N PN   Brennan Barbara J BJ   Le Pogam Sophie S   Nájera Isabel I   Petric Rosemary R   Tran Jonathan Q JQ   Kulkarni Rohit R   Zhang Ying Y   Smith Patrick P   Yetzer Ellen S ES   Shulman Nancy S NS  

Antimicrobial agents and chemotherapy 20131202 2


Danoprevir (DNV) is a hepatitis C virus (HCV) protease inhibitor that achieves high sustained virologic response (SVR) rates in combination with peginterferon alfa-2a-ribavirin in treatment-naive HCV genotype 1 (G1)-infected patients. This study explored the efficacy and safety of ritonavir-boosted DNV (DNVr) plus peginterferon alfa-2a-ribavirin in G1-infected prior peginterferon-ribavirin null responders. Null responders (<2-log10 reduction in HCV RNA level at week 12) were given an open-label  ...[more]

Similar Datasets

| S-EPMC4606559 | biostudies-literature
| S-EPMC1860092 | biostudies-literature
| S-EPMC4713467 | biostudies-literature
| S-EPMC4806200 | biostudies-literature
| S-EPMC4929089 | biostudies-literature
| S-EPMC3736350 | biostudies-literature
| S-EPMC3691800 | biostudies-literature
| S-EPMC4318982 | biostudies-literature
| S-EPMC4931749 | biostudies-literature
| S-EPMC6207807 | biostudies-literature