Source
Institute of Clinical Medicine, College of Medicine, Kaohsiung Medical University, Kaohsiung, Taiwan; Hepatobiliary Division, Department of Internal Medicine, Kaohsiung Medical University Hospital, Kaohsiung, Taiwan; Department of Occupational Medicine, Kaohsiung Municipal Ta-Tung Hospital, Kaohsiung Medical University Hospital, Kaohsiung Medical University, Kaohsiung, Taiwan.
Abstract
BACKGROUND AND AIM:
Host interleukin-28B (IL-28B) genetic variants determine a sustained virological responsese (SVR) in hepatitis C virus genotype 1 (HCV-1) treatment-naïve patients. Its impact on treatment-experienced Asian patients with peginterferon/ribavirin in is to be elucidated.
METHODS:
IL-28B rs8099917 genotype was determined in 70 HCV-1 treatment-experienced patients retreated with 48-week peginterferon/ribavirin.
RESULTS:
The SVR rate was 60.0% and was significantly higher in previous relapsers than in non-responders (72.7% and 13.3%, P<0.001). Multivariate analysis revealed that the most important factor predictive of an SVR was previous relapse (Odds ratio [OR]/95% C.I.: 14.76/2.72-80.06, P=0.002), followed by the carriage of rs8099917 TT genotype (OR/ 95% C.I.: 7.67/1.27-46.49, P=0.03). Comparing to patients with TG/GG genotype, those with TT genotype had significantly higher rates of rapid virological response (29.3% vs. 0%, P=0.03), end-of-treatment virological response (86.2% vs. 50.0%, P=0.01), SVR (69.0% vs. 16.7%, P=0.002) and lower relapse rate (22.0 % vs. 66.7%, P=0.04). The SVR rate was similarly low between previous non-responders with different rs8099917 genotypes (12.5% vs. 14.3%, P=1). On the contrary, previous relapsers with rs8099917 TT genotype had a significantly higher SVR rate than those who carried rs8099917 TG/GG genotype (78.0 % vs. 20.0%, P=0.02). Stepwise logistic regression analysis revealed that the only factor predictive of an SVR in previous relapsers was the carriage of rs809997 TT genotype (OR/ 95% CI:18.50/1.82-188.39, P=0.014).
CONCLUSIONS:
Host IL-28B genetic variants played a role in Asian relapsers but not non-responders retreated with peginterferon/ribavirin. Direct antiviral agents might be possibly avoidable in Asian relapsers with favorable IL-28B genotype.