Cost-Effectiveness of Treatments for Genotype 1 Hepatitis C Virus Infection in Non-VA and VA Populations

Background: Chronic hepatitis C viral (HCV) infection affects millions of Americans. Health care systems face complex choices between highly efficacious, costly treatments. This study assessed the cost-effectiveness of treatments for chronic, genotype 1 HCV monoinfected, treatment-naïve individuals...

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Main Authors: Shan Liu PhD, Paul G. Barnett PhD, Mark Holodniy MD, Jeanie Lo MPH, Vilija R. Joyce MS, Risha Gidwani DrPH, Steven M. Asch MD, MPH, Douglas K. Owens MD, MS, Jeremy D. Goldhaber-Fiebert PhD
Format: Article
Language:English
Published: SAGE Publishing 2016-09-01
Series:MDM Policy & Practice
Online Access:https://doi.org/10.1177/2381468316671946
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spelling doaj-eba9f6cb2d884e6dbd0ec76771e49d9d2020-11-25T03:55:44ZengSAGE PublishingMDM Policy & Practice2381-46832016-09-01110.1177/2381468316671946Cost-Effectiveness of Treatments for Genotype 1 Hepatitis C Virus Infection in Non-VA and VA PopulationsShan Liu PhDPaul G. Barnett PhDMark Holodniy MDJeanie Lo MPHVilija R. Joyce MSRisha Gidwani DrPHSteven M. Asch MD, MPHDouglas K. Owens MD, MSJeremy D. Goldhaber-Fiebert PhDBackground: Chronic hepatitis C viral (HCV) infection affects millions of Americans. Health care systems face complex choices between highly efficacious, costly treatments. This study assessed the cost-effectiveness of treatments for chronic, genotype 1 HCV monoinfected, treatment-naïve individuals in the Department of Veterans Affairs (VA) and general US health care systems. Methods: The study used a decision-analytic Markov model, employing appropriate payer perspectives and time horizons, and discounting benefits and costs at 3% annually. Interventions included the following: sofosbuvir/ledipasvir (SOF-LDV); ombitasvir/paritaprevir/ritonavir/dasabuvir (3D); sofosbuvir/simeprevir (SOF-SMV); sofosbuvir/pegylated interferon/ribavirin (SOF-RBV-PEG); boceprevir/pegylated interferon/ribavirin (BOC-RBV-PEG); and pegylated interferon/ribavirin (PEG-RBV). Outcomes were sustained virologic response (SVR), advanced liver disease, costs, quality adjusted life years (QALYs), and incremental cost-effectiveness. Results: SOF-LDV and 3D achieve high SVR rates, reducing advanced liver disease (>20% relative to no treatment), and increasing QALYs by >2 years per person. For the non-VA population, at current prices ($5040 per week for SOF-LDV; $4796 per week for 3D), SOF-LDV’s lifetime cost ($293,370) is $18,000 lower than 3D’s because of its shorter duration in subgroups. SOF-LDV costs $17,100 per QALY gained relative to no treatment. 3D costs $208,000 per QALY gained relative to SOF-LDV. Both dominate other treatments and are even more cost-effective for the VA, though VA aggregate treatment costs still exceed $4 billion at SOF-LDV prices of $3308 per week. Drug prices strongly determine relative cost-effectiveness for SOF-LDV and 3D; with price reductions of 20% to 30% depending on health system, 3D could be cost-effective relative to SOF-LDV. We currently lack head-to-head regimen effectiveness trials. Conclusions: New HCV treatments are cost-effective in multiple health care systems if trial-estimated efficacy is achieved in practice, though, at current prices, total expenditures could present substantial challenges.https://doi.org/10.1177/2381468316671946
collection DOAJ
language English
format Article
sources DOAJ
author Shan Liu PhD
Paul G. Barnett PhD
Mark Holodniy MD
Jeanie Lo MPH
Vilija R. Joyce MS
Risha Gidwani DrPH
Steven M. Asch MD, MPH
Douglas K. Owens MD, MS
Jeremy D. Goldhaber-Fiebert PhD
spellingShingle Shan Liu PhD
Paul G. Barnett PhD
Mark Holodniy MD
Jeanie Lo MPH
Vilija R. Joyce MS
Risha Gidwani DrPH
Steven M. Asch MD, MPH
Douglas K. Owens MD, MS
Jeremy D. Goldhaber-Fiebert PhD
Cost-Effectiveness of Treatments for Genotype 1 Hepatitis C Virus Infection in Non-VA and VA Populations
MDM Policy & Practice
author_facet Shan Liu PhD
Paul G. Barnett PhD
Mark Holodniy MD
Jeanie Lo MPH
Vilija R. Joyce MS
Risha Gidwani DrPH
Steven M. Asch MD, MPH
Douglas K. Owens MD, MS
Jeremy D. Goldhaber-Fiebert PhD
author_sort Shan Liu PhD
title Cost-Effectiveness of Treatments for Genotype 1 Hepatitis C Virus Infection in Non-VA and VA Populations
title_short Cost-Effectiveness of Treatments for Genotype 1 Hepatitis C Virus Infection in Non-VA and VA Populations
title_full Cost-Effectiveness of Treatments for Genotype 1 Hepatitis C Virus Infection in Non-VA and VA Populations
title_fullStr Cost-Effectiveness of Treatments for Genotype 1 Hepatitis C Virus Infection in Non-VA and VA Populations
title_full_unstemmed Cost-Effectiveness of Treatments for Genotype 1 Hepatitis C Virus Infection in Non-VA and VA Populations
title_sort cost-effectiveness of treatments for genotype 1 hepatitis c virus infection in non-va and va populations
publisher SAGE Publishing
series MDM Policy & Practice
issn 2381-4683
publishDate 2016-09-01
description Background: Chronic hepatitis C viral (HCV) infection affects millions of Americans. Health care systems face complex choices between highly efficacious, costly treatments. This study assessed the cost-effectiveness of treatments for chronic, genotype 1 HCV monoinfected, treatment-naïve individuals in the Department of Veterans Affairs (VA) and general US health care systems. Methods: The study used a decision-analytic Markov model, employing appropriate payer perspectives and time horizons, and discounting benefits and costs at 3% annually. Interventions included the following: sofosbuvir/ledipasvir (SOF-LDV); ombitasvir/paritaprevir/ritonavir/dasabuvir (3D); sofosbuvir/simeprevir (SOF-SMV); sofosbuvir/pegylated interferon/ribavirin (SOF-RBV-PEG); boceprevir/pegylated interferon/ribavirin (BOC-RBV-PEG); and pegylated interferon/ribavirin (PEG-RBV). Outcomes were sustained virologic response (SVR), advanced liver disease, costs, quality adjusted life years (QALYs), and incremental cost-effectiveness. Results: SOF-LDV and 3D achieve high SVR rates, reducing advanced liver disease (>20% relative to no treatment), and increasing QALYs by >2 years per person. For the non-VA population, at current prices ($5040 per week for SOF-LDV; $4796 per week for 3D), SOF-LDV’s lifetime cost ($293,370) is $18,000 lower than 3D’s because of its shorter duration in subgroups. SOF-LDV costs $17,100 per QALY gained relative to no treatment. 3D costs $208,000 per QALY gained relative to SOF-LDV. Both dominate other treatments and are even more cost-effective for the VA, though VA aggregate treatment costs still exceed $4 billion at SOF-LDV prices of $3308 per week. Drug prices strongly determine relative cost-effectiveness for SOF-LDV and 3D; with price reductions of 20% to 30% depending on health system, 3D could be cost-effective relative to SOF-LDV. We currently lack head-to-head regimen effectiveness trials. Conclusions: New HCV treatments are cost-effective in multiple health care systems if trial-estimated efficacy is achieved in practice, though, at current prices, total expenditures could present substantial challenges.
url https://doi.org/10.1177/2381468316671946
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