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Efficacy and Safety of Danoprevir-Ritonavir plus Peginterferon Alfa-2a–Ribavirin in Hepatitis C Virus Genotype 1 Prior Null Responders
- Source :
- Antimicrobial Agents and Chemotherapy. 58:1136-1145
- Publication Year :
- 2014
- Publisher :
- American Society for Microbiology, 2014.
-
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 (10 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-log 10 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.)
- Subjects :
- Cyclopropanes
Male
Hepacivirus
Isoindoles
Viral Nonstructural Proteins
Pharmacology
medicine.disease_cause
Gastroenterology
Polyethylene Glycols
chemistry.chemical_compound
Medicine
Pharmacology (medical)
Sulfonamides
biology
Danoprevir
virus diseases
Alanine Transaminase
Middle Aged
Viral Load
Recombinant Proteins
Treatment Outcome
Infectious Diseases
RNA, Viral
Drug Therapy, Combination
Female
Viral load
Peginterferon alfa-2a
medicine.drug
Adult
medicine.medical_specialty
Genotype
Lactams
Proline
Lactams, Macrocyclic
Hepatitis C virus
Alpha interferon
Antiviral Agents
Drug Administration Schedule
Internal medicine
Drug Resistance, Viral
Ribavirin
Humans
Ritonavir
business.industry
Interferon-alpha
Hepatitis C, Chronic
digestive system diseases
chemistry
Alanine transaminase
Mutation
biology.protein
business
Subjects
Details
- ISSN :
- 10986596 and 00664804
- Volume :
- 58
- Database :
- OpenAIRE
- Journal :
- Antimicrobial Agents and Chemotherapy
- Accession number :
- edsair.doi.dedup.....9caf3cf8a33ebaa435799ecc4b188d9c
- Full Text :
- https://doi.org/10.1128/aac.01515-13