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Cost Effectiveness and Cost Containment in the Era of Interferon-Free Therapies to Treat Hepatitis C Virus Genotype 1
Open accessAbstract
Background: Interferon-free regimens to treat hepatitis C virus (HCV) genotype 1 are effective but costly. At this time, payers in the United States use strategies to control costs including (1) limiting treatment to those with advanced disease and (2) negotiating price discounts in exchange for exclusivity. Methods: We used Monte Carlo simulation to investigate budgetary impact and cost effectiveness of these treatment policies and to identify strategies that balance access with cost control. Outcomes included nondiscounted 5-year payer cost per 10000 HCV-infected patients and incremental cost-effectiveness ratios. Results: We found that the budgetary impact of HCV treatment is high, with 5-year undiscounted costs of $1.0 billion to 2.3 billion per 10000 HCV-infected patients depending on regimen choices. Among noncirrhotic patients, using the least costly interferon-free regimen leads to the lowest payer costs with negligible difference in clinical outcomes, even when the lower cost regimen is less convenient and/or effective. Among cirrhotic patients, more effective but costly regimens remain cost effective. Controlling costs by restricting treatment to those with fibrosis stage 2 or greater disease was cost ineffective for any patient type compared with treating all patients. Conclusions: Treatment strategies using interferon-free therapies to treat all HCV-infected persons are cost effective, but short-term cost is high. Among noncirrhotic patients, using the least costly interferon-free regimen, even if it is not single tablet or once daily, is the cost-control strategy that results in best outcomes. Restricting treatment to patients with more advanced disease often results in worse outcomes than treating all patients, and it is not preferred.
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Some drugs that were not a good value for money at higher prices later became acceptable options when prices were lowered, as observed in hepatitis C.
“our team and others found that some drugs that were not a good value for money at higher prices, later became acceptable options when prices were lowered.44,45”
From Economic Evaluation of Extended-Release Buprenorphine for Persons With Opioid Use Disorder (2023) · cites this paper as [45]
The Results (Cost Control by Negotiating Price Discounts and Requiring Use of Preferred Drugs; page unavailable) show that an HCV regimen could meet the cost-effectiveness threshold at a lower cost but exceed it at a higher cost. The Conclusions also say lower drug costs improve cost effectiveness. These are modeled price comparisons, not evidence that particular drugs later became acceptable after their prices actually fell. (LLM, conf=0.84)
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Barua, S., Greenwald, R., Grebely, J., Dore, G. J., Swan, T., & Taylor, L. E. (2015) · Annals of Internal Medicine · doi:10.7326/m15-0406 · Cited by 401
Linas, B. P., Barter, D. M., Morgan, J. R., Pho, M. T., Leff, J. A., Schackman, B. R., Horsburgh, C. R., Assoumou, S. A., Salomon, J. A., Weinstein, M. C., et al. (2015) · Annals of Internal Medicine · doi:10.7326/m14-1313 · Cited by 101
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Research works printed but not linked: 52
- Chhatwal, 2015, Cost-effectiveness and budget impact of hepatitis C virus treatment with sofosbuvir and ledipasvir in the United States, Ann Intern Med, 162, 397, 10.7326/M14-1336 · DOI
- Najafzadeh, 2015, Cost-effectiveness of novel regimens for the treatment of hepatitis C virus, Ann Intern Med, 162, 407, 10.7326/M14-1152 · DOI
- Rein, 2015, The cost-effectiveness, health benefits, and financial costs of new antiviral treatments for hepatitis C virus, Clin Infect Dis, 61, 157, 10.1093/cid/civ220 · DOI
- Leidner, 2015, Cost-effectiveness of hepatitis C treatment for patients in early stages of liver disease, Hepatology, 61, 1860, 10.1002/hep.27736 · DOI
- Chahal, 2016, Cost-effectiveness of early treatment of hepatitis C virus genotype 1 by stage of liver fibrosis in a US treatment-naive population, JAMA Intern Med, 176, 65, 10.1001/jamainternmed.2015.6011 · DOI
- Denniston, 2014, Chronic hepatitis C virus infection in the United States, National Health and Nutrition Examination Survey 2003 to 2010, Ann Intern Med, 160, 293, 10.7326/M13-1133 · DOI
- New York State Department of Health, 2015, New York State Medicaid Drug Utilization Review Meeting February 26
- Linas, 2014, The hepatitis C cascade of care: identifying priorities to improve clinical outcomes, PLoS One, 9, e97317, 10.1371/journal.pone.0097317 · DOI
- Gold, 1996, Cost-Effectiveness in Health and Medicine, 10.1093/oso/9780195108248.001.0001 · DOI · Paper page
- Sullivan, 2014, Budget impact analysis-principles of good practice: report of the ISPOR 2012 Budget Impact Analysis Good Practice II Task Force, Value Health, 17, 5, 10.1016/j.jval.2013.08.2291 · DOI
- Chong, 2003, Health-state utilities and quality of life in hepatitis C patients, Am J Gastroenterol, 98, 630, 10.1111/j.1572-0241.2003.07332.x · DOI
- Grieve, 2006, Cost effectiveness of interferon alpha or peginterferon alpha with ribavirin for histologically mild chronic hepatitis C, Gut, 55, 1332, 10.1136/gut.2005.064774 · DOI
- Stein, 2002, Screening for hepatitis C among injecting drug users and in genitourinary medicine clinics: systematic reviews of effectiveness, modelling study and national survey of current practice, Health Technol Assess, 6, 1, 10.3310/hta6310 · DOI
- Bruno, 2009, Predicting mortality risk in patients with compensated HCV-induced cirrhosis: a long-term prospective study, Am J Gastroenterol, 104, 1147, 10.1038/ajg.2009.31 · DOI
- Arias, 2012, United States life tables, 2008, Natl Vital Stat Rep, 61, 1
- McHutchison, 2009, Peginterferon alfa-2b or alfa-2a with ribavirin for treatment of hepatitis C infection, N Engl J Med, 361, 580, 10.1056/NEJMoa0808010 · DOI
- Jacobson, 2014, Simeprevir with pegylated interferon alfa 2a plus ribavirin in treatment-naive patients with chronic hepatitis C virus genotype 1 infection (QUEST-1): a phase 3, randomised, double-blind, placebo-controlled trial, Lancet, 384, 403, 10.1016/S0140-6736(14)60494-3 · DOI
- Manns, 2014, Simeprevir with pegylated interferon alfa 2a or 2b plus ribavirin in treatment-naive patients with chronic hepatitis C virus genotype 1 infection (QUEST-2): a randomised, double-blind, placebo-controlled phase 3 trial, Lancet, 384, 414, 10.1016/S0140-6736(14)60538-9 · DOI
- Afdhal, 2014, Ledipasvir and sofosbuvir for previously treated HCV genotype 1 infection, N Engl J Med, 370, 1483, 10.1056/NEJMoa1316366 · DOI
- Afdhal, 2014, Ledipasvir and sofosbuvir for untreated HCV genotype 1 infection, N Engl J Med, 370, 1889, 10.1056/NEJMoa1402454 · DOI
- Lawitz, 2014, Simeprevir plus sofosbuvir, with or without ribavirin, to treat chronic infection with hepatitis C virus genotype 1 in non-responders to pegylated interferon and ribavirin and treatment-naive patients: the COSMOS randomised study, Lancet, 384, 1756, 10.1016/S0140-6736(14)61036-9 · DOI
- Sulkowski, 2014, Daclatasvir plus sofosbuvir for previously treated or untreated chronic HCV infection, N Engl J Med, 370, 211, 10.1056/NEJMoa1306218 · DOI
- Poynard, 2012, Relative performances of FibroTest, Fibroscan, and biopsy for the assessment of the stage of liver fibrosis in patients with chronic hepatitis C: a step toward the truth in the absence of a gold standard, J Hepatol, 56, 541, 10.1016/j.jhep.2011.08.007 · DOI
- Welzel, 2015, Daclatasvir plus sofosbuvir with or without ribavirin for the treatment of HCV in patients with severe liver disease: interim results of a multicenter compassionate use program
- Kowdley, 2014, Ledipasvir and sofosbuvir for 8 or 12 weeks for chronic HCV without cirrhosis, N Engl J Med, 370, 1879, 10.1056/NEJMoa1402355 · DOI
- Ferenci, 2014, ABT-450/r-ombitasvir and dasabuvir with or without ribavirin for HCV, N Engl J Med, 370, 1983, 10.1056/NEJMoa1402338 · DOI
- Zeuzem, 2014, Retreatment of HCV with ABT-450/r-ombitasvir and dasabuvir with ribavirin, N Engl J Med, 370, 1604, 10.1056/NEJMoa1401561 · DOI
- Poordad, 2014, ABT-450/r-ombitasvir and dasabuvir with ribavirin for hepatitis C with cirrhosis, N Engl J Med, 370, 1973, 10.1056/NEJMoa1402869 · DOI
- Lawitz, 2013, Sofosbuvir for previously untreated chronic hepatitis C infection, N Engl J Med, 368, 1878, 10.1056/NEJMoa1214853 · DOI
- Agency for Healthcare Research and Quality, Total health services-mean and median expenses per person with expense and distribution of expenses by source of payment: medical expenditure panel survey household component data. Generated interactively
- Davis, 2011, Direct economic burden of chronic hepatitis C virus in a United States managed care population, J Clin Gastroenterol, 45, e17, 10.1097/MCG.0b013e3181e12c09 · DOI
- Levinson, Medicaid drug price comparisons: average manufacturer price to published prices 2005
- Sullivan, 2006, Preference-based EQ-5D index scores for chronic conditions in the United States, Med Decis Making, 26, 410, 10.1177/0272989X06290495 · DOI
- Sherman, 2013, 904 health-related quality-of-life among Genotype 1 treatment-experienced chronic hepatitis C patients: post-hoc analyses from the Realize Study, J Hepatol, 58, S372, 10.1016/S0168-8278(13)60906-X · DOI
- Stepanova, 2014, Patients’ preferences and health utility assessment with SF-6D and EQ-5D in patients with chronic hepatitis C treated with sofosbuvir regimens, Aliment Pharmacol Ther, 40, 676, 10.1111/apt.12880 · DOI
- Schackman, 2008, Quality-of-life tradeoffs for hepatitis C treatment: do patients and providers agree?, Med Decis Making, 28, 233, 10.1177/0272989X07311753 · DOI
- Townsend, 2011, Structural frameworks and key model parameters in cost-effectiveness analyses for current and future treatments of chronic hepatitis C, Value Health, 14, 1068, 10.1016/j.jval.2011.06.006 · DOI
- van der Meer, 2012, Association between sustained virological response and all-cause mortality among patients with chronic hepatitis C and advanced hepatic fibrosis, JAMA, 308, 2584, 10.1001/jama.2012.144878 · DOI
- AASLD/IDSA/IAS–USA, Recommendations for testing, managing, and treating hepatitis C
- U.S. Food and Drug Administration, FDA Drug Safety Communication: FDA warns of serious liver injury risk with hepatitis C treatments Viekira Pak and Technivie
- Zeremski, 2016, Fibrosis progression in patients with chronic hepatitis C virus infection, J Infect Dis, 214, 1164, 10.1093/infdis/jiw332 · DOI
- Younossi, 2015, Systematic review: patient-reported outcomes in chronic hepatitis C–the impact of liver disease and new treatment regimens, Aliment Pharmacol Ther, 41, 497, 10.1111/apt.13090 · DOI
- National Viral Hepatitis Roundtable, Center for Health Law & Policy Innovation, Hepatitis C: The State of Medicaid Access
- Ampel, United Health expands hepatitis C drug coverage to settle national class action
- Thein, 2008, Estimation of stage-specific fibrosis progression rates in chronic hepatitis C virus infection: a meta-analysis and meta-regression, Hepatology, 48, 418, 10.1002/hep.22375 · DOI
- Poynard, 1997, Natural history of liver fibrosis progression in patients with chronic hepatitis C. The OBSVIRC, METAVIR, CLINIVIR, and DOSVIRC groups, Lancet, 349, 825, 10.1016/S0140-6736(96)07642-8 · DOI · Paper page
- Gilead Sciences, Havoni Package Insert
- Reddy, 2015, Ledipasvir and sofosbuvir in patients with genotype 1 hepatitis C virus infection and compensated cirrhosis: an integrated safety and efficacy analysis, Hepatology, 62, 79, 10.1002/hep.27826 · DOI
- United States Department of Health and Human Services Center for Medicare Services, Physician Fee Schedule
- United States Department of Health and Human Services Center for Medicare Services, Clinical Diagnostic Laboratory Fee Schedule
- Chaiwat, 2009, Early packed red blood cell transfusion and acute respiratory distress syndrome after trauma, Anesthesiology, 110, 351, 10.1097/ALN.0b013e3181948a97 · DOI
- Gao, 2012, Impact of adverse events on costs and quality of life in protease inhibitor-based combination therapy for hepatitis C, Expert Rev Pharmacoecon Outcomes Res, 12, 335, 10.1586/erp.12.10 · DOI
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Sorted by citations
Economic Evaluation of Extended-Release Buprenorphine for Persons With Opioid Use Disorder
Flam-Ross, J. M., Marsh, E., Weitz, M., Savinkina, A., Schackman, B. R., Wang, J., Madushani, R. W. M. A., Morgan, J. R., Barocas, J. A., Walley, A. Y., et al. (2023) · JAMA Network Open · doi:10.1001/jamanetworkopen.2023.29583 · Cited by 21
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Metadata
- Authors
- Linas, B. P., Morgan, J. R., Pho, M. T., Leff, J. A., Schackman, B. R., Horsburgh, C. R., Assoumou, S. A., Salomon, J. A., Weinstein, M. C., Freedberg, K. A., & Kim, A. Y.
- Affiliations
- Boston University (US)
- Boston Medical Center (US)
- University of Chicago (US)
- Weill Cornell Medicine (US)
- Harvard University (US)
- Massachusetts General Hospital (US)
- Corresponding author
- Linas, Benjamin P.
- ORCID
- Venue
- Open Forum Infectious Diseases
- Publisher
- Oxford University Press (OUP)
- Published
- 2016-12-27
- Volume
- 4
- Issue
- 1
- Pages
- ofw266-ofw266
- ISSN
- 2328-8957 (ISSN-L)
- PMC
- PMC5414108
- OpenAlex
- W2563301157
- Cited by
- 19
- References
- 2
- Citations by year
- 2023: 3 · 2022: 7 · 2019: 2 · 2018: 6 · 2017: 1
- FWCI
- 2.17
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Licence
- Locations
- Open Forum Infectious Diseases (publishedVersion, cc-by-nc-nd)
- Europe PMC (PubMed Central) (publishedVersion, cc-by-nc-nd)
- PubMed Central (publishedVersion, cc-by-nc-nd)
- PubMed (publishedVersion)
- Digital Access to Scholarship at Harvard (DASH) (Harvard University) (submittedVersion, cc-by)
- Funders
- National Institute on Drug Abuse (R01DA031059,, P30DA040500)
- National Institutes of Health
- Topics
- Health Sciences › Medicine › Hepatology › Hepatitis C virus research
- Social Sciences › Economics, Econometrics and Finance › Economics and Econometrics › Health Systems, Economic Evaluations, Quality of Life
- Social Sciences › Economics, Econometrics and Finance › Economics and Econometrics › Pharmaceutical Economics and Policy
- Keywords
- hepatitis C virus, HCV genotype 1, interferon-free therapy, cost-effectiveness, cost containment, budget impact, liver cirrhosis, fibrosis stage, treatment access, discounts, antiviral therapy
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