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Utility of hepatitis C viral load monitoring on direct-acting antiviral therapy.


ABSTRACT:

Background

Hepatitis C virus (HCV) RNA loads serve as predictors of treatment response during interferon-based therapy. We evaluated the predictive ability of HCV RNA levels at end of treatment (EOT) for sustained virologic response (SVR12) during interferon-sparing direct-acting antiviral therapies.

Methods

HCV genotype 1-infected, treatment-naive patients were treated with sofosbuvir and ribavirin for 24 weeks (n = 55), sofosbuvir and ledipasvir for 12 weeks (n = 20), sofosbuvir, ledipasvir, and GS-9669 for 6 weeks (n = 20), or sofosbuvir, ledipasvir, and GS-9451 for 6 weeks (n = 19). Measurements of HCV RNA were performed using the Roche COBAS TaqMan HCV test and the Abbott RealTime HCV assay. Positive predictive value (PPV) and negative predictive value (NPV) of HCV RNA less than the lower limit of quantification (ResultsAll 55 patients treated with sofosbuvir and ribavirin had HCV RNA ConclusionsContrary to past experience with interferon-containing treatments, low levels of quantifiable HCV RNA at EOT do not preclude treatment success.

SUBMITTER: Sidharthan S 

PROVIDER: S-EPMC4834854 | biostudies-literature | 2015 Jun

REPOSITORIES: biostudies-literature

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Publications

Utility of hepatitis C viral load monitoring on direct-acting antiviral therapy.

Sidharthan Sreetha S   Kohli Anita A   Sims Zayani Z   Nelson Amy A   Osinusi Anu A   Masur Henry H   Kottilil Shyam S  

Clinical infectious diseases : an official publication of the Infectious Diseases Society of America 20150302 12


<h4>Background</h4>Hepatitis C virus (HCV) RNA loads serve as predictors of treatment response during interferon-based therapy. We evaluated the predictive ability of HCV RNA levels at end of treatment (EOT) for sustained virologic response (SVR12) during interferon-sparing direct-acting antiviral therapies.<h4>Methods</h4>HCV genotype 1-infected, treatment-naive patients were treated with sofosbuvir and ribavirin for 24 weeks (n = 55), sofosbuvir and ledipasvir for 12 weeks (n = 20), sofosbuvir  ...[more]

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