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Cost-effectiveness analysis of azacitidine in the treatment of high-risk myelodysplastic syndromes in Spain

BACKGROUND: The objective of the study was to analyse whether azacitidine is a cost-effective option for the treatment of myelodysplastic syndrome in the Spanish setting compared with conventional care regimens, including best supportive care, low dose chemotherapy and standard dose chemotherapy. ME...

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Autores principales: Crespo, Carlos, Moreno, Estela, Sierra, Jordi, Serip, Suzan, Rubio, Marta
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4029489/
https://www.ncbi.nlm.nih.gov/pubmed/24314138
http://dx.doi.org/10.1186/2191-1991-3-28
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author Crespo, Carlos
Moreno, Estela
Sierra, Jordi
Serip, Suzan
Rubio, Marta
author_facet Crespo, Carlos
Moreno, Estela
Sierra, Jordi
Serip, Suzan
Rubio, Marta
author_sort Crespo, Carlos
collection PubMed
description BACKGROUND: The objective of the study was to analyse whether azacitidine is a cost-effective option for the treatment of myelodysplastic syndrome in the Spanish setting compared with conventional care regimens, including best supportive care, low dose chemotherapy and standard dose chemotherapy. METHODS: A life-time Markov model was constructed to evaluate the cost-effectiveness of azacitidine compared with conventional care regimens. The health states modelled were: myelodysplastic syndrome, acute myeloid leukemia and death. Variables measured included survival rates, progression probabilities and quality of life indicators. Resource use and cost data reflect the Spanish context. The analysis was performed from the Spanish National Health System perspective, discounting both costs (in 2012 euros) and future effects at 3%. The time horizon considered was end-of-life. Results were expressed in cost per quality-adjusted life-year gained and cost per life-year gained and compared with cost-effectiveness thresholds. RESULTS: According to the current use of each conventional care regimens options in Spain, azacitidine resulted in €34,673 per quality-adjusted life-year gained (€28,891 per life-year gained) with an increase of 1.89 in quality-adjusted life-years (2.26 in life-years). Azacitidine was superior to best supportive care and low dose chemotherapy in terms of quality-adjusted life-years gained, 1.82 and 2.03, respectively (life-years 2.16 vs. best supportive care, 2.39 vs. low dose chemotherapy). Treatment with azacitidine resulted in longer survival time and thus longer treatment time and lifetime costs. The incremental cost-effectiveness ratio was €39,610 per quality-adjusted life-year gained vs. best supportive care and €30,531 per quality-adjusted life-year gained vs. low dose chemotherapy (€33,111 per life-year gained vs. best supportive care and €25,953 per life-year gained vs. low dose chemotherapy). CONCLUSIONS: The analysis showed that the use of azacitidine in the treatment of high-risk myelodysplastic syndrome is a cost-effective option compared with conventional care regimen options used in the Spanish setting and had an incremental cost-effectiveness ratio within the range of the thresholds accepted by health authorities.
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spelling pubmed-40294892014-06-05 Cost-effectiveness analysis of azacitidine in the treatment of high-risk myelodysplastic syndromes in Spain Crespo, Carlos Moreno, Estela Sierra, Jordi Serip, Suzan Rubio, Marta Health Econ Rev Research BACKGROUND: The objective of the study was to analyse whether azacitidine is a cost-effective option for the treatment of myelodysplastic syndrome in the Spanish setting compared with conventional care regimens, including best supportive care, low dose chemotherapy and standard dose chemotherapy. METHODS: A life-time Markov model was constructed to evaluate the cost-effectiveness of azacitidine compared with conventional care regimens. The health states modelled were: myelodysplastic syndrome, acute myeloid leukemia and death. Variables measured included survival rates, progression probabilities and quality of life indicators. Resource use and cost data reflect the Spanish context. The analysis was performed from the Spanish National Health System perspective, discounting both costs (in 2012 euros) and future effects at 3%. The time horizon considered was end-of-life. Results were expressed in cost per quality-adjusted life-year gained and cost per life-year gained and compared with cost-effectiveness thresholds. RESULTS: According to the current use of each conventional care regimens options in Spain, azacitidine resulted in €34,673 per quality-adjusted life-year gained (€28,891 per life-year gained) with an increase of 1.89 in quality-adjusted life-years (2.26 in life-years). Azacitidine was superior to best supportive care and low dose chemotherapy in terms of quality-adjusted life-years gained, 1.82 and 2.03, respectively (life-years 2.16 vs. best supportive care, 2.39 vs. low dose chemotherapy). Treatment with azacitidine resulted in longer survival time and thus longer treatment time and lifetime costs. The incremental cost-effectiveness ratio was €39,610 per quality-adjusted life-year gained vs. best supportive care and €30,531 per quality-adjusted life-year gained vs. low dose chemotherapy (€33,111 per life-year gained vs. best supportive care and €25,953 per life-year gained vs. low dose chemotherapy). CONCLUSIONS: The analysis showed that the use of azacitidine in the treatment of high-risk myelodysplastic syndrome is a cost-effective option compared with conventional care regimen options used in the Spanish setting and had an incremental cost-effectiveness ratio within the range of the thresholds accepted by health authorities. Springer 2013-12-05 /pmc/articles/PMC4029489/ /pubmed/24314138 http://dx.doi.org/10.1186/2191-1991-3-28 Text en Copyright © 2013 Crespo et al.; licensee Springer. This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Crespo, Carlos
Moreno, Estela
Sierra, Jordi
Serip, Suzan
Rubio, Marta
Cost-effectiveness analysis of azacitidine in the treatment of high-risk myelodysplastic syndromes in Spain
title Cost-effectiveness analysis of azacitidine in the treatment of high-risk myelodysplastic syndromes in Spain
title_full Cost-effectiveness analysis of azacitidine in the treatment of high-risk myelodysplastic syndromes in Spain
title_fullStr Cost-effectiveness analysis of azacitidine in the treatment of high-risk myelodysplastic syndromes in Spain
title_full_unstemmed Cost-effectiveness analysis of azacitidine in the treatment of high-risk myelodysplastic syndromes in Spain
title_short Cost-effectiveness analysis of azacitidine in the treatment of high-risk myelodysplastic syndromes in Spain
title_sort cost-effectiveness analysis of azacitidine in the treatment of high-risk myelodysplastic syndromes in spain
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4029489/
https://www.ncbi.nlm.nih.gov/pubmed/24314138
http://dx.doi.org/10.1186/2191-1991-3-28
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