Predictability of IL-28B-polymorphism on protease-inhibitor-based triple-therapy in chronic HCV-genotype-1 patients: A meta-analysis
Nicolae-Catalin Mechie, Christian R\"over, Silke Cameron, Ahmad, Amanzada

TL;DR
This meta-analysis shows that IL-28B polymorphism, especially the CC genotype, predicts better treatment response in chronic HCV genotype-1 patients undergoing protease-inhibitor-based triple-therapy, with variability among different drugs.
Contribution
It provides a comprehensive analysis of how IL-28B genotype influences treatment outcomes across various protease inhibitors in HCV therapy.
Findings
IL-28B-CC genotype patients have higher SVR rates.
Predictive value of IL-28B varies with different protease inhibitors.
Treatment-naive or experienced status does not affect IL-28B's predictive power.
Abstract
AIM: To investigate the predictability of interleukin-28B single nucleotide polymorphism rs12979860 with respect to sustained virological response (SVR) in chronically hepatitis C virus (HCV) genotype-1 patients treated with a protease-inhibitor and pegylated interferon- (Peg-INF-) based triple-therapy. METHODS: We searched PubMed, the Cochrane Library and Web of Knowledge for studies regarding the interleukin 28B (IL-28B)-genotype and protease-inhibitor based triple-therapy. Ten studies with 2707 patients were included into this meta-analysis. We used regression methods in order to investigate determinants of SVR. RESULTS: IL-28B-CC-genotype patients achieved higher SVR rates (odds 5.34, CI: 3.81-7.49) than IL-28B-non-CC-genotype patients (1.88, CI: 1.43-2.48) receiving triple-therapy. The line of therapy (treatment-na\"ive or -experienced for Peg-INF-) did…
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