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Societal preferences for adjuvant melanoma health states: UK and Australia

BACKGROUND: No studies have measured preference-based utility weights for specific toxicities and outcomes associated with approved and investigational adjuvant treatments for patients with resected high-risk melanoma. METHODS: A cross-sectional study was conducted in the United Kingdom and Australi...

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Autores principales: Middleton, Mark R., Atkins, Michael B., Amos, Kaitlan, Wang, Peter Feng, Kotapati, Srividya, Sabater, Javier, Beusterien, Kathleen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5646133/
https://www.ncbi.nlm.nih.gov/pubmed/29041898
http://dx.doi.org/10.1186/s12885-017-3673-y
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author Middleton, Mark R.
Atkins, Michael B.
Amos, Kaitlan
Wang, Peter Feng
Kotapati, Srividya
Sabater, Javier
Beusterien, Kathleen
author_facet Middleton, Mark R.
Atkins, Michael B.
Amos, Kaitlan
Wang, Peter Feng
Kotapati, Srividya
Sabater, Javier
Beusterien, Kathleen
author_sort Middleton, Mark R.
collection PubMed
description BACKGROUND: No studies have measured preference-based utility weights for specific toxicities and outcomes associated with approved and investigational adjuvant treatments for patients with resected high-risk melanoma. METHODS: A cross-sectional study was conducted in the United Kingdom and Australia to obtain utilities for 14 adjuvant melanoma health states. One-on-one interviews were conducted using standard gamble; utility weights range from 0.0, dead, to 1.0, full health. Supplemental risk questions also were asked. RESULTS: Among 155 participants (52% male; mean age, 46 years) “adjuvant treatment no toxicities” (0.89) was most preferred, followed by “induction treatment” (0.88), and “no treatment” (0.86). Participants least preferred “cancer recurrence” (0.62); the utility for “cancer recurrence and 10-year survival with treatment” was 0.70. Disutilities for grade 2 toxicities ranged from −0.06 for fatigue to −0.13 for hypophysitis. The mean maximum acceptable risk of a life-threatening event ranged from 30% for a 6% increase in the chance of remaining cancer free over 3 years to 40% for an 18% increase; Australian respondents were willing to take higher risks. CONCLUSION: Reproducible health utilities for adjuvant melanoma health states were obtained from the general population in two countries. These utilities can be incorporated into treatment-specific cost-effectiveness evaluations. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12885-017-3673-y) contains supplementary material, which is available to authorized users.
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spelling pubmed-56461332017-10-26 Societal preferences for adjuvant melanoma health states: UK and Australia Middleton, Mark R. Atkins, Michael B. Amos, Kaitlan Wang, Peter Feng Kotapati, Srividya Sabater, Javier Beusterien, Kathleen BMC Cancer Research Article BACKGROUND: No studies have measured preference-based utility weights for specific toxicities and outcomes associated with approved and investigational adjuvant treatments for patients with resected high-risk melanoma. METHODS: A cross-sectional study was conducted in the United Kingdom and Australia to obtain utilities for 14 adjuvant melanoma health states. One-on-one interviews were conducted using standard gamble; utility weights range from 0.0, dead, to 1.0, full health. Supplemental risk questions also were asked. RESULTS: Among 155 participants (52% male; mean age, 46 years) “adjuvant treatment no toxicities” (0.89) was most preferred, followed by “induction treatment” (0.88), and “no treatment” (0.86). Participants least preferred “cancer recurrence” (0.62); the utility for “cancer recurrence and 10-year survival with treatment” was 0.70. Disutilities for grade 2 toxicities ranged from −0.06 for fatigue to −0.13 for hypophysitis. The mean maximum acceptable risk of a life-threatening event ranged from 30% for a 6% increase in the chance of remaining cancer free over 3 years to 40% for an 18% increase; Australian respondents were willing to take higher risks. CONCLUSION: Reproducible health utilities for adjuvant melanoma health states were obtained from the general population in two countries. These utilities can be incorporated into treatment-specific cost-effectiveness evaluations. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12885-017-3673-y) contains supplementary material, which is available to authorized users. BioMed Central 2017-10-17 /pmc/articles/PMC5646133/ /pubmed/29041898 http://dx.doi.org/10.1186/s12885-017-3673-y Text en © The Author(s). 2017 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 Article
Middleton, Mark R.
Atkins, Michael B.
Amos, Kaitlan
Wang, Peter Feng
Kotapati, Srividya
Sabater, Javier
Beusterien, Kathleen
Societal preferences for adjuvant melanoma health states: UK and Australia
title Societal preferences for adjuvant melanoma health states: UK and Australia
title_full Societal preferences for adjuvant melanoma health states: UK and Australia
title_fullStr Societal preferences for adjuvant melanoma health states: UK and Australia
title_full_unstemmed Societal preferences for adjuvant melanoma health states: UK and Australia
title_short Societal preferences for adjuvant melanoma health states: UK and Australia
title_sort societal preferences for adjuvant melanoma health states: uk and australia
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5646133/
https://www.ncbi.nlm.nih.gov/pubmed/29041898
http://dx.doi.org/10.1186/s12885-017-3673-y
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