Original Article

Vol. 27 No. 2 (2016): 2016.27.2-Turkish Journal of Gastroenterology

Can the Abbott RealTime hepatitis C virus assay be used to predict therapeutic outcomes in hepatitis C virus-infected patients undergoing triple therapy?

Main Article Content

Yohei Noguchi
Michihiro Suzuki
Fumio Itoh
Kazuhiko Koike
Hiroshi Yotsuyanagi
Hiroshi Yasuda
Hiroyuki Yamamoto
Kazunari Nakahara
Junko Shima
Toshiya Ishii
Hiroki Ikeda
Yasunobu Fukuda
Tetsuya Hiraishi
Nobuhiro Hattori
Ryuta Shigefuku
Kotaro Matsunaga
Nobuyuki Matsumoto
Tsunamasa Watanabe
Chiaki Okuse

Abstract

Background/Aims: We compared the predictive abilities of the Abbott Real Time hepatitis C virus (HCV) assay (ART) with those of standard serum HCV ribonucleic acid (RNA) detection methods in patients undergoing triple therapy, which involves treatment with a protease inhibitor combined with pegylated interferon and ribavirin.<o:p></o:p>
 
Materials and Methods: In this study, 28 patients underwent triple therapy. The hepatitis C virus ribonucleic acid (HCV RNA) level of each patient was measured at weeks 0, 4, 8, and 12 after the initiation of therapy using the Roche COBAS AmpliPrep/COBAS TaqMan HCV assay version 1.0 (CAP/CTM v1.0) and ART. <o:p></o:p>
 
Results: At week 8 after the initiation of therapy, the sustained virological response (SVR) rate among patients who tested negative and positive for HCV RNA using CAP/CTM v1.0, was 80.0% (20/25) and 33.3% (1/3), and using ART, it was 91.3% (21/23) and 0.0% (0/5), respectively. Although at week 8, the predictive capability of CAP/CTM v1.0 was 78.5%, ART was found to be a more accurate predictor of future SVR status with a rate of 92.9%.<o:p></o:p>
 
Conclusion: These results indicate that the presence or absence of serum HCV RNA, evaluated using ART at week 8 after the initiation of therapy, may be useful for predicting therapeutic outcomes in patients receiving triple therapy. <o:p></o:p>
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