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Cost Effectiveness of Avelumab for Metastatic Merkel Cell Carcinoma

BACKGROUND: Metastatic Merkel cell carcinoma (mMCC) is a rare and aggressive skin cancer. Until recently, there were no licensed treatment options for patients with mMCC, and prognosis was poor. A cost-effectiveness analysis was conducted for avelumab, a newly available treatment option for mMCC, ve...

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Autores principales: Bullement, Ash, Nathan, Paul, Willis, Anna, Amin, Amerah, Lilley, Cameron, Stapelkamp, Ceilidh, Hatswell, Anthony, Pescott, Chris, Bharmal, Murtuza
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6710317/
https://www.ncbi.nlm.nih.gov/pubmed/30680676
http://dx.doi.org/10.1007/s41669-018-0115-y
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author Bullement, Ash
Nathan, Paul
Willis, Anna
Amin, Amerah
Lilley, Cameron
Stapelkamp, Ceilidh
Hatswell, Anthony
Pescott, Chris
Bharmal, Murtuza
author_facet Bullement, Ash
Nathan, Paul
Willis, Anna
Amin, Amerah
Lilley, Cameron
Stapelkamp, Ceilidh
Hatswell, Anthony
Pescott, Chris
Bharmal, Murtuza
author_sort Bullement, Ash
collection PubMed
description BACKGROUND: Metastatic Merkel cell carcinoma (mMCC) is a rare and aggressive skin cancer. Until recently, there were no licensed treatment options for patients with mMCC, and prognosis was poor. A cost-effectiveness analysis was conducted for avelumab, a newly available treatment option for mMCC, versus standard care (SC), from a UK National Health Service perspective. METHODS: A partitioned survival model was developed to assess the lifetime costs and effects of avelumab versus SC. Data from the JAVELIN Merkel 200 trial (NCT02155647) were used to inform estimates of quality-adjusted life-years (QALYs). Unit costs and associated frequencies of use were informed by published literature and clinical expert opinion. Results were presented as incremental cost-effectiveness ratios (ICERs, i.e. the cost per QALY gained) for treatment-experienced (TE) and treatment-naïve (TN) patients. Uncertainty was explored through a range of sensitivity analyses. RESULTS: Discounting costs and QALYs at 3.5% per annum, avelumab was associated with ICERs of £35,274 (TE)/£39,178 (TN) per QALY gained. Probabilistic sensitivity analysis results demonstrated that avelumab was associated with an 88.3% (TE)/69.3% (TN) probability of being cost effective at a willingness-to-pay threshold for end-of-life treatments of £50,000 per QALY gained. Results were most sensitive to alternative survival extrapolations and dosing assumptions. CONCLUSIONS: The analysis results suggest that avelumab is likely to be a cost-effective treatment option for UK mMCC patients. The results for TN patients are subject to some uncertainty, and a confirmatory analysis will be conducted with more mature data.
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spelling pubmed-67103172019-09-09 Cost Effectiveness of Avelumab for Metastatic Merkel Cell Carcinoma Bullement, Ash Nathan, Paul Willis, Anna Amin, Amerah Lilley, Cameron Stapelkamp, Ceilidh Hatswell, Anthony Pescott, Chris Bharmal, Murtuza Pharmacoecon Open Original Research Article BACKGROUND: Metastatic Merkel cell carcinoma (mMCC) is a rare and aggressive skin cancer. Until recently, there were no licensed treatment options for patients with mMCC, and prognosis was poor. A cost-effectiveness analysis was conducted for avelumab, a newly available treatment option for mMCC, versus standard care (SC), from a UK National Health Service perspective. METHODS: A partitioned survival model was developed to assess the lifetime costs and effects of avelumab versus SC. Data from the JAVELIN Merkel 200 trial (NCT02155647) were used to inform estimates of quality-adjusted life-years (QALYs). Unit costs and associated frequencies of use were informed by published literature and clinical expert opinion. Results were presented as incremental cost-effectiveness ratios (ICERs, i.e. the cost per QALY gained) for treatment-experienced (TE) and treatment-naïve (TN) patients. Uncertainty was explored through a range of sensitivity analyses. RESULTS: Discounting costs and QALYs at 3.5% per annum, avelumab was associated with ICERs of £35,274 (TE)/£39,178 (TN) per QALY gained. Probabilistic sensitivity analysis results demonstrated that avelumab was associated with an 88.3% (TE)/69.3% (TN) probability of being cost effective at a willingness-to-pay threshold for end-of-life treatments of £50,000 per QALY gained. Results were most sensitive to alternative survival extrapolations and dosing assumptions. CONCLUSIONS: The analysis results suggest that avelumab is likely to be a cost-effective treatment option for UK mMCC patients. The results for TN patients are subject to some uncertainty, and a confirmatory analysis will be conducted with more mature data. Springer International Publishing 2019-01-24 /pmc/articles/PMC6710317/ /pubmed/30680676 http://dx.doi.org/10.1007/s41669-018-0115-y Text en © The Author(s) 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 International License (http://creativecommons.org/licenses/by-nc/4.0/), which permits any noncommercial 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.
spellingShingle Original Research Article
Bullement, Ash
Nathan, Paul
Willis, Anna
Amin, Amerah
Lilley, Cameron
Stapelkamp, Ceilidh
Hatswell, Anthony
Pescott, Chris
Bharmal, Murtuza
Cost Effectiveness of Avelumab for Metastatic Merkel Cell Carcinoma
title Cost Effectiveness of Avelumab for Metastatic Merkel Cell Carcinoma
title_full Cost Effectiveness of Avelumab for Metastatic Merkel Cell Carcinoma
title_fullStr Cost Effectiveness of Avelumab for Metastatic Merkel Cell Carcinoma
title_full_unstemmed Cost Effectiveness of Avelumab for Metastatic Merkel Cell Carcinoma
title_short Cost Effectiveness of Avelumab for Metastatic Merkel Cell Carcinoma
title_sort cost effectiveness of avelumab for metastatic merkel cell carcinoma
topic Original Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6710317/
https://www.ncbi.nlm.nih.gov/pubmed/30680676
http://dx.doi.org/10.1007/s41669-018-0115-y
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