Protease inhibitor use for chronic hepatitis C infection in special populations: a review of the clinical evidence and guidelines

CADTH
Record ID 32012000656
English
Authors' recommendations: At present, there is insufficient evidence to determine the clinical benefit and harm of adding boceprevir or telaprevir to PR in patients with CHC co-infected with HIV. CHC patients who are null responders to previous PR therapy may benefit from telaprevir-PR, although the response rate is expected to be lower than in the general CHC population. There are no RCT data on this population for boceprevir-PR. Similar to the overall trial populations in the included studies, patients with CHC infection and metavir scores of F0 or F1 (telaprevir) or F0-F2 (boceprevir) achieved higher SVR rates with protease inhibitors added to PR over PR alone. Response rates with PI-PR were generally higher at earlier stages of fibrosis compared with later stages in treatment-naïve patients, but not in treatment-experienced patients.
Details
Project Status: Completed
Year Published: 2012
English language abstract: An English language summary is available
Publication Type: Not Assigned
Country: Canada
MeSH Terms
  • Humans
  • Protease Inhibitors
  • Hepatitis C, Chronic
Contact
Organisation Name: Canadian Agency for Drugs and Technologies in Health
Contact Address: 600-865 Carling Avenue, Ottawa, ON K1S 5S8 Canada. Tel: +1 613 226 2553; Fax: +1 613 226 5392;
Contact Name: requests@cadth.ca
Contact Email: requests@cadth.ca
Copyright: Canadian Agency for Drugs and Technologies in Health (CADTH)
This is a bibliographic record of a published health technology assessment from a member of INAHTA or other HTA producer. No evaluation of the quality of this assessment has been made for the HTA database.