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Article: Cost–Utility of All-Oral Direct-Acting Antiviral Regimens for the Treatment of Genotype 1 Chronic Hepatitis C Virus-Infected Patients in Hong Kong
Title | Cost–Utility of All-Oral Direct-Acting Antiviral Regimens for the Treatment of Genotype 1 Chronic Hepatitis C Virus-Infected Patients in Hong Kong |
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Authors | |
Keywords | Hepatitis C Chronic Cost–utility analysis Direct-acting antiviral agents Elbasvir/grazoprevir |
Issue Date | 2020 |
Publisher | Springer New York LLC. The Journal's web site is located at http://springerlink.metapress.com/openurl.asp?genre=journal&issn=0163-2116 |
Citation | Digestive Diseases and Sciences, 2020, v. 66, p. 1315-1326 How to Cite? |
Abstract | Background:
Direct-acting antivirals (DAAs) are entering the hepatitis C virus (HCV) treatment landscape in Hong Kong, prompting the need for cost–effectiveness evaluations of these interventions to enable optimal use of healthcare resources.
Aims:
This study aimed to compare the cost–effectiveness of DAAs to standard-of-care pegylated interferon plus ribavirin (RBV) in treatment-naïve patients without significant liver fibrosis and to compare different DAAs in patients who are treatment-experienced and/or have advanced liver disease.
Methods:
A Markov model was constructed to evaluate cost–effectiveness over a lifetime time horizon from the payer perspective. The target population was treatment-naïve and treatment-experienced HCV genotype 1 patients, stratified by degree of liver fibrosis. The model consists of 16 health states encompassing METAVIR fibrosis score (F0–F4), treatment success or failure, decompensated cirrhosis, hepatocellular carcinoma, liver transplant, and liver-related death. The proportions of patients achieving sustained virologic response were obtained from clinical trials. Other inputs were obtained from published and local data. The primary outcome was incremental cost–utility ratio for each DAA versus pegylated interferon + ribavirin and among different DAAs.
Results:
In treatment-naïve F0–2 HCV patients, all DAAs were cost-effective in genotype 1a and daclatasvir + asunaprevir, elbasvir/grazoprevir, ledipasvir/sofosbuvir, and glecaprevir/pibrentasvir were cost-effective compared to pegylated interferon + ribavirin in genotype 1b. In genotypes 1a and 1b, treatment-experienced patients, and F3–4 patients, elbasvir/grazoprevir was the least costly DAA and economically dominant over most other DAAs.
Conclusions:
DAAs can be a cost-effective option for the treatment of genotype 1 HCV patients in Hong Kong, and elbasvir/grazoprevir is cost-effective. |
Persistent Identifier | http://hdl.handle.net/10722/282530 |
ISSN | 2021 Impact Factor: 3.487 2020 SCImago Journal Rankings: 1.140 |
ISI Accession Number ID |
DC Field | Value | Language |
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dc.contributor.author | Yuen, M-F | - |
dc.contributor.author | Liu, S-H | - |
dc.contributor.author | Seto, WK | - |
dc.contributor.author | Mak, L-Y | - |
dc.contributor.author | Corman, SL | - |
dc.contributor.author | Hsu, DC | - |
dc.contributor.author | Lee, MYK | - |
dc.contributor.author | Khan, TK | - |
dc.contributor.author | Puenpatom, A | - |
dc.date.accessioned | 2020-05-15T05:29:19Z | - |
dc.date.available | 2020-05-15T05:29:19Z | - |
dc.date.issued | 2020 | - |
dc.identifier.citation | Digestive Diseases and Sciences, 2020, v. 66, p. 1315-1326 | - |
dc.identifier.issn | 0163-2116 | - |
dc.identifier.uri | http://hdl.handle.net/10722/282530 | - |
dc.description.abstract | Background: Direct-acting antivirals (DAAs) are entering the hepatitis C virus (HCV) treatment landscape in Hong Kong, prompting the need for cost–effectiveness evaluations of these interventions to enable optimal use of healthcare resources. Aims: This study aimed to compare the cost–effectiveness of DAAs to standard-of-care pegylated interferon plus ribavirin (RBV) in treatment-naïve patients without significant liver fibrosis and to compare different DAAs in patients who are treatment-experienced and/or have advanced liver disease. Methods: A Markov model was constructed to evaluate cost–effectiveness over a lifetime time horizon from the payer perspective. The target population was treatment-naïve and treatment-experienced HCV genotype 1 patients, stratified by degree of liver fibrosis. The model consists of 16 health states encompassing METAVIR fibrosis score (F0–F4), treatment success or failure, decompensated cirrhosis, hepatocellular carcinoma, liver transplant, and liver-related death. The proportions of patients achieving sustained virologic response were obtained from clinical trials. Other inputs were obtained from published and local data. The primary outcome was incremental cost–utility ratio for each DAA versus pegylated interferon + ribavirin and among different DAAs. Results: In treatment-naïve F0–2 HCV patients, all DAAs were cost-effective in genotype 1a and daclatasvir + asunaprevir, elbasvir/grazoprevir, ledipasvir/sofosbuvir, and glecaprevir/pibrentasvir were cost-effective compared to pegylated interferon + ribavirin in genotype 1b. In genotypes 1a and 1b, treatment-experienced patients, and F3–4 patients, elbasvir/grazoprevir was the least costly DAA and economically dominant over most other DAAs. Conclusions: DAAs can be a cost-effective option for the treatment of genotype 1 HCV patients in Hong Kong, and elbasvir/grazoprevir is cost-effective. | - |
dc.language | eng | - |
dc.publisher | Springer New York LLC. The Journal's web site is located at http://springerlink.metapress.com/openurl.asp?genre=journal&issn=0163-2116 | - |
dc.relation.ispartof | Digestive Diseases and Sciences | - |
dc.rights | This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License. | - |
dc.subject | Hepatitis C | - |
dc.subject | Chronic | - |
dc.subject | Cost–utility analysis | - |
dc.subject | Direct-acting antiviral agents | - |
dc.subject | Elbasvir/grazoprevir | - |
dc.title | Cost–Utility of All-Oral Direct-Acting Antiviral Regimens for the Treatment of Genotype 1 Chronic Hepatitis C Virus-Infected Patients in Hong Kong | - |
dc.type | Article | - |
dc.identifier.email | Yuen, M-F: mfyuen@hku.hk | - |
dc.identifier.email | Liu, S-H: drkliu@hku.hk | - |
dc.identifier.email | Seto, WK: wkseto@hku.hk | - |
dc.identifier.email | Mak, L-Y: lungyi@HKUCC-COM.hku.hk | - |
dc.identifier.authority | Yuen, M-F=rp00479 | - |
dc.identifier.authority | Seto, WK=rp01659 | - |
dc.identifier.authority | Mak, L-Y=rp02668 | - |
dc.description.nature | published_or_final_version | - |
dc.identifier.doi | 10.1007/s10620-020-06281-8 | - |
dc.identifier.scopus | eid_2-s2.0-85084489236 | - |
dc.identifier.hkuros | 309970 | - |
dc.identifier.volume | 66 | - |
dc.identifier.spage | 1315 | - |
dc.identifier.epage | 1326 | - |
dc.identifier.isi | WOS:000632475400045 | - |
dc.publisher.place | United States | - |
dc.identifier.issnl | 0163-2116 | - |