Portal de Periódicos da CAPES

Efficacy and Safety of Pegylated Interferon Combined with Ribavirin for the Treatment of Older Patients with Chronic Hepatitis C

2010; Oxford University Press; Volume: 201; Issue: 5 Linguagem: Inglês

10.1086/650470

1537-6613

Chung‐Feng Huang, Jeng‐Fu Yang, Chia‐Yen Dai, Jee‐Fu Huang, Nai‐Jen Hou, Ming‐Yen Hsieh, Zu‐Yau Lin, Shinn‐Cherng Chen, Ming‐Yuh Hsieh, Liang‐Yen Wang, Wen‐Yu Chang, Wan‐Long Chuang, Ming‐Lung Yu,

Hepatitis B Virus Studies

Background. The present study evaluated the efficacy and safety of pegylated interferon (PegIFN)/ribavirin treatment in elderly patients with hepatitis C virus (HCV) infection. Methods. Seventy elderly patients with hepatitis C virus (HCV) infection (group A; age, ⩾65 years) and 140 sex- and HCV genotype-matched controls (group B; age, 50–64 years) were allocated to receive a PegIFN-α-2a/ribavirin standard-of-care regimen. Results. Group A had a significantly higher rate of treatment discontinuation (21.4% vs 6.4%; P = .001) and grade 3 or 4 adverse events (34.3% vs 20%; P = .002) than group B. In intention-to-treat analysis, the sustained virologic response (SVR) rate was substantially lower in group A than in group B (67.1% vs 78.6%; P = .07). The inferiority of the SVR rate in group A was observed among patients with HCV genotype 1 (HCV-1) (51.9% vs 75.9%; P = .03) but not among patients with HCV genotype 2 or 3 (HCV-2/3) (76.7% vs 80.2%; P = .65). Among patients in group A who had a rapid virologic response, those infected with HCV-1 and those infected with HCV-2/3 had similar SVR rates (80% and 87.9%, respectively). For patients receiving treatment for >80% of its expected duration, SVR rates were similar between the 2 groups (80.4% vs 82.6%, respectively), regardless of viral genotype. Conclusions. Older patients with HCV infection, especially those in the subgroup infected with HCV-1, had a greater frequency of adverse events and poorer adherence to the standard-of-care regimen, which may be the major reason for treatment inferiority. Trial registration.Clinicaltrials.gov identifier NCT00629824.