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Rapid Viral Response and Sustained Treatment Outcome: A Comparison between 2 HCV RNA Assays

In this study, published in the Journal of Medical Virology (July 8, 2008), 50 consecutive patients with genotype 2 or 3 chronic hepatitis C virus (HCV) infection were treated with 135 microgram weekly pegylated interferon alfa-2a (Pegasys) and daily ribavirin (11 mg/kg body weight) for 24 weeks.

Rapid virological response (RVR) at week 4, end-of-treatment response, and sustained virological response (SVR) were analyzed using 2 different HCV RNA quantitation methods: the Cobas Amplicor Monitor test with a sensitivity of 600 IU/mL, and the TaqMan test with a sensitivity of 15 IU/mL, respectively.

Results

The more sensitive TaqMan test better differentiated patients with RVR who ultimately achieved SVR.

97% (32/33) of patients with RVR versus 75% (12/16) without RVR as determined by the TaqMan assay (P < 0.017).

The corresponding figures for the Cobas Amplicor test were 91% (41/45) versus (80%), a non-significant difference.

Based on these findings, the Swedish study authors concluded, "The more sensitive TaqMan test yielded a lower number of patients with RVR than the less sensitive Amplicor Monitor test, but predicted SVR in a higher percentage of patients with RVR than the Amplicor Monitor test."

In addition, they noted, "A RVR, meaning HCV RNA levels <15 IU/ml, predicted a SVR in 97% of patients with genotype 2 or 3."

Division of Infectious Diseases, Department of Medicine, and Division of Virology, Department of Laboratory Medicine, Karolinska Institutet, Karolinska University Hospital, Stockholm, Sweden.

8/05/08

Reference
T Carlsson, A Quist and O Weiland. Rapid viral response and treatment outcome in genotype 2 and 3 chronic hepatitis C: comparison between two HCV RNA quantitation methods. Journal of Medical Virology 80(5): 803-807. May 2008. (Abstract)

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 


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