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Physician preferences for non-metastatic castration-resistant prostate cancer treatment
BACKGROUND: Recent approvals of second-generation androgen receptor inhibitors (SGARIs) have changed the treatment landscape for non-metastatic castration-resistant prostate cancer (nmCRPC). These SGARIs have similar efficacy but differ in safety profiles. We used a discrete choice experiment to exp...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7310549/ https://www.ncbi.nlm.nih.gov/pubmed/32571276 http://dx.doi.org/10.1186/s12894-020-00631-4 |
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author | Srinivas, Sandy Mohamed, Ateesha F. Appukkuttan, Sreevalsa Botteman, Marc Ng, Xinyi Joshi, Namita Horodniceanu, Erica Waldeck, A. Reginald Simmons, Stacey J |
author_facet | Srinivas, Sandy Mohamed, Ateesha F. Appukkuttan, Sreevalsa Botteman, Marc Ng, Xinyi Joshi, Namita Horodniceanu, Erica Waldeck, A. Reginald Simmons, Stacey J |
author_sort | Srinivas, Sandy |
collection | PubMed |
description | BACKGROUND: Recent approvals of second-generation androgen receptor inhibitors (SGARIs) have changed the treatment landscape for non-metastatic castration-resistant prostate cancer (nmCRPC). These SGARIs have similar efficacy but differ in safety profiles. We used a discrete choice experiment to explore how United States physicians make treatment decisions between adverse events (AEs) and survival gains in nmCRPC, a largely asymptomatic disease. METHODS: Treating physicians (n = 149) participated in an online survey that included 14 treatment choice questions, each comparing 2 hypothetical treatment profiles, which varied in terms of 5 safety and 2 efficacy attributes. We described safety attributes (fatigue, skin rash, cognitive problems, falls, and fractures) in terms of severity and frequency, and efficacy attributes (overall survival [OS] and time to pain progression) in terms of duration of effect. We used a random parameters logit model to estimate preference weights and importance scores for each attribute. We also estimated the amount of survival gain physicians were willing to trade for a reduction in specific AEs between treatment options. RESULTS: Physicians placed more importance on survival than on time to pain progression, and viewed a reduction in cognitive problems from severe to none, a reduction in risk of a serious fracture from 8% to none, and a reduction in fatigue from severe to none as the most important safety attributes. Physicians were willing to forego 9.1 and 6.6 months of OS, respectively, to reduce cognitive problems and fatigue from severe to mild-to-moderate. To reduce the risk of a serious fracture from 8 to 5% and 5% to none, physicians were willing to trade 3.9 and 5.3 months of OS, respectively. CONCLUSIONS: Physicians were willing to trade substantial amounts of survival to avoid AEs between hypothetical treatments. These results emphasize the importance of carefully balancing therapies’ benefits and risks to ultimately optimize the overall quality of nmCRPC patients’ survival. Nonetheless, it is noted that the results from the study sample of 149 physicans may not be representative of the viewpoints of all nmCRPC-treating physicians. |
format | Online Article Text |
id | pubmed-7310549 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-73105492020-06-24 Physician preferences for non-metastatic castration-resistant prostate cancer treatment Srinivas, Sandy Mohamed, Ateesha F. Appukkuttan, Sreevalsa Botteman, Marc Ng, Xinyi Joshi, Namita Horodniceanu, Erica Waldeck, A. Reginald Simmons, Stacey J BMC Urol Research Article BACKGROUND: Recent approvals of second-generation androgen receptor inhibitors (SGARIs) have changed the treatment landscape for non-metastatic castration-resistant prostate cancer (nmCRPC). These SGARIs have similar efficacy but differ in safety profiles. We used a discrete choice experiment to explore how United States physicians make treatment decisions between adverse events (AEs) and survival gains in nmCRPC, a largely asymptomatic disease. METHODS: Treating physicians (n = 149) participated in an online survey that included 14 treatment choice questions, each comparing 2 hypothetical treatment profiles, which varied in terms of 5 safety and 2 efficacy attributes. We described safety attributes (fatigue, skin rash, cognitive problems, falls, and fractures) in terms of severity and frequency, and efficacy attributes (overall survival [OS] and time to pain progression) in terms of duration of effect. We used a random parameters logit model to estimate preference weights and importance scores for each attribute. We also estimated the amount of survival gain physicians were willing to trade for a reduction in specific AEs between treatment options. RESULTS: Physicians placed more importance on survival than on time to pain progression, and viewed a reduction in cognitive problems from severe to none, a reduction in risk of a serious fracture from 8% to none, and a reduction in fatigue from severe to none as the most important safety attributes. Physicians were willing to forego 9.1 and 6.6 months of OS, respectively, to reduce cognitive problems and fatigue from severe to mild-to-moderate. To reduce the risk of a serious fracture from 8 to 5% and 5% to none, physicians were willing to trade 3.9 and 5.3 months of OS, respectively. CONCLUSIONS: Physicians were willing to trade substantial amounts of survival to avoid AEs between hypothetical treatments. These results emphasize the importance of carefully balancing therapies’ benefits and risks to ultimately optimize the overall quality of nmCRPC patients’ survival. Nonetheless, it is noted that the results from the study sample of 149 physicans may not be representative of the viewpoints of all nmCRPC-treating physicians. BioMed Central 2020-06-22 /pmc/articles/PMC7310549/ /pubmed/32571276 http://dx.doi.org/10.1186/s12894-020-00631-4 Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. 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 in a credit line to the data. |
spellingShingle | Research Article Srinivas, Sandy Mohamed, Ateesha F. Appukkuttan, Sreevalsa Botteman, Marc Ng, Xinyi Joshi, Namita Horodniceanu, Erica Waldeck, A. Reginald Simmons, Stacey J Physician preferences for non-metastatic castration-resistant prostate cancer treatment |
title | Physician preferences for non-metastatic castration-resistant prostate cancer treatment |
title_full | Physician preferences for non-metastatic castration-resistant prostate cancer treatment |
title_fullStr | Physician preferences for non-metastatic castration-resistant prostate cancer treatment |
title_full_unstemmed | Physician preferences for non-metastatic castration-resistant prostate cancer treatment |
title_short | Physician preferences for non-metastatic castration-resistant prostate cancer treatment |
title_sort | physician preferences for non-metastatic castration-resistant prostate cancer treatment |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7310549/ https://www.ncbi.nlm.nih.gov/pubmed/32571276 http://dx.doi.org/10.1186/s12894-020-00631-4 |
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