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10.1002/hep.27151

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C4077973!4077973 !24677184
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suck abstract from ncbi


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pmid24677184
      Hepatology 2014 ; 60 (1 ): 37-45
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  • Cost analysis of sofosbuvir/ribavirin versus sofosbuvir/simeprevir for genotype 1 hepatitis C virus in interferon-ineligible/intolerant individuals #MMPMID24677184
  • Hagan LM ; Sulkowski MS ; Schinazi RF
  • Hepatology 2014[Jul]; 60 (1 ): 37-45 PMID24677184 show ga
  • Treatment guidance for chronic hepatitis C (CHC) released by the American Association for the Study of Liver Diseases (AASLD) and the Infectious Diseases Society of America (IDSA) offers two options for interferon (IFN)-ineligible/intolerant individuals with genotype 1 infection: sofosbuvir/ribavirin (SOF/RBV) for 24 weeks or sofosbuvir/simeprevir (SOF/SMV) for 12 weeks. A 24-week course of SOF/RBV costs approximately US$169,000, with sustained virologic response (SVR) rates ranging from 52% to 84%; 12 weeks of SOF/SMV costs approximately $150,000, with SVR between 89% and 100%. Because SOF/SMV is currently used off-label, debate exists among physicians and payers about whether it should be prescribed and covered. This article presents a cost-effectiveness analysis of these two treatment regimens accounting for costs of drugs, treatment-related medical care, retreatment for individuals who do not achieve SVR, and natural history of continued HCV infection after failed retreatment. Analysis uses a Markov model with a lifetime horizon and a societal perspective. In the base-case scenario, SOF/SMV dominated SOF/RBV in a modeled 50-year-old cohort of treatment-naïve and -experienced subjects, excluding those who failed earlier therapy with telaprevir or boceprevir. SOF/SMV yielded lower costs and more quality-adjusted life years (QALYs) for the average subject, compared to SOF/RBV ($165,336 and 14.69 QALYs vs. $243,586 and 14.45 QALYs, respectively). In base-case cost analysis, the SOF/SMV treatment strategy saved $91,590 per SVR, compared to SOF/RBV. Under all one-way sensitivity scenarios, SOF/SMV remained dominant and resulted in cost savings. CONCLUSIONS: These results suggest that a 12-week course of SOF/SMV is a more cost-effective treatment for genotype 1 CHC than 24 weeks of SOF/RBV among IFN-ineligible/intolerant individuals, supporting the AASLD/IDSA guidance and offering implications for both clinical and regulatory decision making as well as pharmaceutical pricing.
  • |*Hepatitis C, Chronic/drug therapy/economics/mortality [MESH]
  • |Antiviral Agents/economics/therapeutic use [MESH]
  • |Cost-Benefit Analysis [MESH]
  • |Drug Costs/*statistics & numerical data [MESH]
  • |Drug Therapy, Combination [MESH]
  • |Genotype [MESH]
  • |Hepacivirus/*drug effects/genetics [MESH]
  • |Heterocyclic Compounds, 3-Ring/*economics/therapeutic use [MESH]
  • |Humans [MESH]
  • |Interferons/therapeutic use [MESH]
  • |Liver Cirrhosis/drug therapy/economics/mortality [MESH]
  • |Markov Chains [MESH]
  • |Middle Aged [MESH]
  • |Quality-Adjusted Life Years [MESH]
  • |Retreatment/economics [MESH]
  • |Ribavirin/*economics/therapeutic use [MESH]
  • |Simeprevir [MESH]
  • |Sofosbuvir [MESH]
  • |Sulfonamides/*economics/therapeutic use [MESH]


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