This study was supported by Korea University Grant (K0812921).The authors who have taken part in this study do not have a relationship with the manufactures of the drug in the past or present and did not receive funding from the manufacturers to carry out this research.
Virologic and biochemical responses to clevudine in patients with chronic HBV infection- associated cirrhosis: data at week 48
Article first published online: 28 MAR 2010
© 2010 Blackwell Publishing Ltd
Journal of Viral Hepatitis
Volume 18, Issue 4, pages 287–293, April 2011
How to Cite
Kim, J. H., Yim, H. J., Jung, E. S., Jung, Y. K., Kim, J. H., Seo, Y. S., Yeon, J. E., Lee, H. S., Um, S. H. and Byun, K. S. (2011), Virologic and biochemical responses to clevudine in patients with chronic HBV infection- associated cirrhosis: data at week 48. Journal of Viral Hepatitis, 18: 287–293. doi: 10.1111/j.1365-2893.2010.01304.x
- Issue published online: 28 MAR 2010
- Article first published online: 28 MAR 2010
- Received October 2009; accepted for publication January 2010
- biochemical response;
- liver cirrhosis;
- virologic response
Summary. Clevudine shows high rates of virologic and biochemical responses in patients with chronic hepatitis B. However, the efficacy and safety of clevudine in patients with cirrhosis are unknown. The aims of this study were to evaluate the safety and to assess the virologic and the biochemical responses to clevudine in patients with cirrhosis with chronic hepatitis B virus (HBV) infection. We reviewed data from treatment-naïve patients with chronic hepatitis B with and without cirrhosis who started clevudine between April 2007 and March 2008 (n = 52, hepatitis B without cirrhosis n = 21 and chronic hepatitis B with cirrhosis n = 31) at Korea University Ansan/Guro Hospital. All of the patients were treated for more than 48 weeks. The mean age was older in the patients with cirrhosis. Baseline HBV DNA levels were 6.9 and 7.78 log copies/mL (P = 0.042), and alanine aminotransferase (ALT) levels were 104.9 and 147.4 IU/L (P = 0.204), for those with and without cirrhosis, respectively. Virologic response (HBV DNA <1000 copies/mL) (87.1%vs 71.4%, P = 0.24) and biochemical response (83.9%vs 80.9%, P = 0.99) at week 48 were not significantly different between the two groups. Early virologic response at week 12 was even higher in the patients with cirrhosis (61.3%vs 28.6%, P = 0.026). Neither ALT flare nor newly onset hepatic decompensation was found in the patients with cirrhosis, whereas ALT flare was transiently observed in 14.3% of the chronic hepatitis group. In conclusion, although clevudine may produce a transient elevation of ALT during the early treatment period, such findings were not observed in patients with cirrhosis and the virologic and biochemical responses of the groups were comparable.