PMID- 18081737 OWN - NLM STAT- MEDLINE DCOM- 20080331 LR - 20181201 IS - 1365-2036 (Electronic) IS - 0269-2813 (Linking) VI - 27 IP - 5 DP - 2008 Mar 1 TI - Peginterferon alfa-2a/ribavirin in hepatitis C virus patients nontolerant or nonresponsive to peginterferon alfa-2b/ribavirin. PG - 433-40 AB - BACKGROUND: Peginterferon alfa-2a/ribavirin treatment resulted in fewer incidences of depression and flu-like symptoms than that of standard interferon/ribavirin, whereas peginterferon alfa-2b/ribavirin and standard interferon/ribavirin treatment resulted in similar incidences of these adverse events (AEs). AIM: To assess the efficacy and safety of peginterferon alfa-2a/ribavirin in genotype 1-infected patients treated for up to 12 weeks with peginterferon alfa-2b/ribavirin but not achieving early virologic response (EVR) (non-EVR) or nontolerant (NT) because of depression, fatigue, flu-like symptoms, or injection-site reactions. METHODS: Nontolerants were treated for an additional 36 weeks and non-EVRs for an additional 60 weeks with peginterferon alfa-2a (180 microg/week)/ribavirin (1000/1200 mg/day). Patients with detectable HCV RNA after 12 weeks were discontinued. RESULTS: Of 25 NTs, 23 (92%) were HCV-RNA negative after 12 weeks on peginterferon alfa-2a/ribavirin and 14 (56%) achieved sustained virologic response. Of 32 non-EVRs to peginterferon alfa-2b/ribavirin, four (13%) achieved EVR with peginterferon alfa-2a/ribavirin and one (3%) achieved sustained virologic response. Four non-EVRs and 0 NTs were withdrawn for AEs; 26 (81%) and 24 (96%), respectively, completed peginterferon alfa-2a/ribavirin treatment or were withdrawn for insufficient response at week 12. In NTs, depression, fatigue, flu-like symptoms, and injection-site reactions declined during treatment. CONCLUSION: Most patients who did not tolerate peginterferon alfa-2b/ribavirin because of AEs, and who completed the full 36-week course of peginterferon alfa-2a/ribavirin treatment, achieved sustained virologic response. FAU - Rustgi, V K AU - Rustgi VK AD - Liver Transplantation Unit, Georgetown University Medical Center, Washington, DC, USA. hepgi@aol.com FAU - Esposito, S AU - Esposito S FAU - Hamzeh, F M AU - Hamzeh FM FAU - Shiffman, M L AU - Shiffman ML LA - eng SI - ClinicalTrials.gov/NCT00087568 PT - Clinical Trial PT - Comparative Study PT - Journal Article PT - Research Support, Non-U.S. Gov't DEP - 20071210 PL - England TA - Aliment Pharmacol Ther JT - Alimentary pharmacology & therapeutics JID - 8707234 RN - 0 (Antiviral Agents) RN - 0 (Interferon alpha-2) RN - 0 (Interferon-alpha) RN - 0 (RNA, Viral) RN - 0 (Recombinant Proteins) RN - 3WJQ0SDW1A (Polyethylene Glycols) RN - 49717AWG6K (Ribavirin) RN - G8RGG88B68 (peginterferon alfa-2b) RN - Q46947FE7K (peginterferon alfa-2a) SB - IM MH - Adult MH - Anemia/chemically induced MH - Antiviral Agents/adverse effects/*therapeutic use MH - Depression/psychology MH - Drug Administration Schedule MH - Drug Therapy, Combination MH - *Drug Tolerance MH - Female MH - Hepacivirus/drug effects/genetics MH - Hepatitis C, Chronic/*drug therapy/genetics MH - Humans MH - Interferon alpha-2 MH - Interferon-alpha/adverse effects/*therapeutic use MH - Male MH - Middle Aged MH - Multicenter Studies as Topic MH - Neutropenia/chemically induced MH - Polyethylene Glycols/adverse effects/*therapeutic use MH - RNA, Viral/drug effects/genetics MH - Recombinant Proteins MH - Ribavirin/adverse effects/*therapeutic use MH - Surveys and Questionnaires MH - Thrombocytopenia/chemically induced MH - Time Factors MH - Viral Load EDAT- 2007/12/18 09:00 MHDA- 2008/04/01 09:00 CRDT- 2007/12/18 09:00 PHST- 2007/12/18 09:00 [pubmed] PHST- 2008/04/01 09:00 [medline] PHST- 2007/12/18 09:00 [entrez] AID - APT3587 [pii] AID - 10.1111/j.1365-2036.2007.03587.x [doi] PST - ppublish SO - Aliment Pharmacol Ther. 2008 Mar 1;27(5):433-40. doi: 10.1111/j.1365-2036.2007.03587.x. Epub 2007 Dec 10.