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Cost-effectiveness of sorafenib versus SBRT for unresectable advanced hepatocellular carcinoma

OBJECTIVE: Stereotactic body radiotherapy (SBRT) has been shown to improve overall survival in patients with advanced hepatocellular carcinoma. This study aimed to assess the cost-effectiveness of SBRT compared to sorafenib which is the only drug for advanced hepatocellular carcinoma. METHODS: A Mar...

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Autores principales: Leung, Henry W. C., Liu, Chung-Feng, Chan, Agnes L. F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4870794/
https://www.ncbi.nlm.nih.gov/pubmed/27193904
http://dx.doi.org/10.1186/s13014-016-0644-4
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author Leung, Henry W. C.
Liu, Chung-Feng
Chan, Agnes L. F.
author_facet Leung, Henry W. C.
Liu, Chung-Feng
Chan, Agnes L. F.
author_sort Leung, Henry W. C.
collection PubMed
description OBJECTIVE: Stereotactic body radiotherapy (SBRT) has been shown to improve overall survival in patients with advanced hepatocellular carcinoma. This study aimed to assess the cost-effectiveness of SBRT compared to sorafenib which is the only drug for advanced hepatocellular carcinoma. METHODS: A Markov decision-analytic model was performed to compare the cost-effectiveness of SBRT and sorafenib for unresectable advanced hepatocellular carcinoma. Patients transitioned between three health states: stable disease, progression disease and death. We calculated the data on cost from the perspective of our National Health Insurance Bureau. Sensitivity analyses were conducted to determine the impact of several variables. RESULTS: The incremental cost effectiveness ratio (ICER) for sorafenib compared to SBRT was NT$3,788,238 per quality-adjusted life year gained (cost/QALY), which was higher than the willingness to pay threshold of Taiwan according to WHO’s guideline. One-way sensitivity analysis revealed that the utility of progression disease for the sorafenib treatment, utility of progression free survival for SBRT, utility of progression free survival for sorafenib, utility of PFS to progression disease for SBRT and transition probability of progression disease to dead for SBRT were the most sensitive parameters in all cost scenarios. The Monte-Carlo simulation demonstrated that the probability of cost-effectiveness at a willingness to pay threshold of NT$ 2,213,145 per QALY was 100 % and 0 % chance for SBRT and sorafenib. CONCLUSION: This study indicated that SBRT for advanced hepatocellular carcinoma is cost-effective at a willingness to pay threshold as defined by WHO guideline in Taiwan.
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spelling pubmed-48707942016-05-19 Cost-effectiveness of sorafenib versus SBRT for unresectable advanced hepatocellular carcinoma Leung, Henry W. C. Liu, Chung-Feng Chan, Agnes L. F. Radiat Oncol Research OBJECTIVE: Stereotactic body radiotherapy (SBRT) has been shown to improve overall survival in patients with advanced hepatocellular carcinoma. This study aimed to assess the cost-effectiveness of SBRT compared to sorafenib which is the only drug for advanced hepatocellular carcinoma. METHODS: A Markov decision-analytic model was performed to compare the cost-effectiveness of SBRT and sorafenib for unresectable advanced hepatocellular carcinoma. Patients transitioned between three health states: stable disease, progression disease and death. We calculated the data on cost from the perspective of our National Health Insurance Bureau. Sensitivity analyses were conducted to determine the impact of several variables. RESULTS: The incremental cost effectiveness ratio (ICER) for sorafenib compared to SBRT was NT$3,788,238 per quality-adjusted life year gained (cost/QALY), which was higher than the willingness to pay threshold of Taiwan according to WHO’s guideline. One-way sensitivity analysis revealed that the utility of progression disease for the sorafenib treatment, utility of progression free survival for SBRT, utility of progression free survival for sorafenib, utility of PFS to progression disease for SBRT and transition probability of progression disease to dead for SBRT were the most sensitive parameters in all cost scenarios. The Monte-Carlo simulation demonstrated that the probability of cost-effectiveness at a willingness to pay threshold of NT$ 2,213,145 per QALY was 100 % and 0 % chance for SBRT and sorafenib. CONCLUSION: This study indicated that SBRT for advanced hepatocellular carcinoma is cost-effective at a willingness to pay threshold as defined by WHO guideline in Taiwan. BioMed Central 2016-05-18 /pmc/articles/PMC4870794/ /pubmed/27193904 http://dx.doi.org/10.1186/s13014-016-0644-4 Text en © Leung et al. 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Leung, Henry W. C.
Liu, Chung-Feng
Chan, Agnes L. F.
Cost-effectiveness of sorafenib versus SBRT for unresectable advanced hepatocellular carcinoma
title Cost-effectiveness of sorafenib versus SBRT for unresectable advanced hepatocellular carcinoma
title_full Cost-effectiveness of sorafenib versus SBRT for unresectable advanced hepatocellular carcinoma
title_fullStr Cost-effectiveness of sorafenib versus SBRT for unresectable advanced hepatocellular carcinoma
title_full_unstemmed Cost-effectiveness of sorafenib versus SBRT for unresectable advanced hepatocellular carcinoma
title_short Cost-effectiveness of sorafenib versus SBRT for unresectable advanced hepatocellular carcinoma
title_sort cost-effectiveness of sorafenib versus sbrt for unresectable advanced hepatocellular carcinoma
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4870794/
https://www.ncbi.nlm.nih.gov/pubmed/27193904
http://dx.doi.org/10.1186/s13014-016-0644-4
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