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Cohort study examining tamoxifen adherence and its relationship to mortality in women with breast cancer

Increasing duration of tamoxifen therapy improves survival in women with breast cancer but the impact of adherence to tamoxifen on mortality is unclear. This study investigated whether women prescribed tamoxifen after surgery for breast cancer adhered to their prescription and whether adherence infl...

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Autores principales: McCowan, C, Shearer, J, Donnan, P T, Dewar, J A, Crilly, M, Thompson, A M, Fahey, T P
Formato: Texto
Lenguaje:English
Publicado: Nature Publishing Group 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2600703/
https://www.ncbi.nlm.nih.gov/pubmed/18985046
http://dx.doi.org/10.1038/sj.bjc.6604758
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author McCowan, C
Shearer, J
Donnan, P T
Dewar, J A
Crilly, M
Thompson, A M
Fahey, T P
author_facet McCowan, C
Shearer, J
Donnan, P T
Dewar, J A
Crilly, M
Thompson, A M
Fahey, T P
author_sort McCowan, C
collection PubMed
description Increasing duration of tamoxifen therapy improves survival in women with breast cancer but the impact of adherence to tamoxifen on mortality is unclear. This study investigated whether women prescribed tamoxifen after surgery for breast cancer adhered to their prescription and whether adherence influenced survival. A retrospective cohort study of all women with incident breast cancer in the Tayside region of Scotland between 1993 and 2002 was linked to encashed prescription records to calculate adherence to tamoxifen. Survival analysis was used to determine the effect of adherence on all-cause mortality. In all 2080 patients formed the study cohort with 1633 (79%) prescribed tamoxifen. The median duration of use was 2.42 years (IQR=1.04–4.89 years). Longer duration was associated with better survival but this varied over time. The hazard ratio for mortality in relation to duration at 2.4 years was 0.85, 95% CI=0.83–0.87. Median adherence to tamoxifen was 93% (interquartile range=84–100%). Adherence <80% was associated with poorer survival, hazard ratio 1.10, 95% CI=1.001–1.21. Persistence with tamoxifen was modest with only 49% continuing therapy for 5 years of those followed up for 5 years or more. Increased duration of tamoxifen reduces the risk of death, although one in two women do not complete the recommended 5-year course of treatment. A significant proportion of women have low adherence to tamoxifen and are at increased risk of death.
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spelling pubmed-26007032009-12-03 Cohort study examining tamoxifen adherence and its relationship to mortality in women with breast cancer McCowan, C Shearer, J Donnan, P T Dewar, J A Crilly, M Thompson, A M Fahey, T P Br J Cancer Clinical Study Increasing duration of tamoxifen therapy improves survival in women with breast cancer but the impact of adherence to tamoxifen on mortality is unclear. This study investigated whether women prescribed tamoxifen after surgery for breast cancer adhered to their prescription and whether adherence influenced survival. A retrospective cohort study of all women with incident breast cancer in the Tayside region of Scotland between 1993 and 2002 was linked to encashed prescription records to calculate adherence to tamoxifen. Survival analysis was used to determine the effect of adherence on all-cause mortality. In all 2080 patients formed the study cohort with 1633 (79%) prescribed tamoxifen. The median duration of use was 2.42 years (IQR=1.04–4.89 years). Longer duration was associated with better survival but this varied over time. The hazard ratio for mortality in relation to duration at 2.4 years was 0.85, 95% CI=0.83–0.87. Median adherence to tamoxifen was 93% (interquartile range=84–100%). Adherence <80% was associated with poorer survival, hazard ratio 1.10, 95% CI=1.001–1.21. Persistence with tamoxifen was modest with only 49% continuing therapy for 5 years of those followed up for 5 years or more. Increased duration of tamoxifen reduces the risk of death, although one in two women do not complete the recommended 5-year course of treatment. A significant proportion of women have low adherence to tamoxifen and are at increased risk of death. Nature Publishing Group 2008-12-02 2008-11-04 /pmc/articles/PMC2600703/ /pubmed/18985046 http://dx.doi.org/10.1038/sj.bjc.6604758 Text en Copyright © 2008 Cancer Research UK https://creativecommons.org/licenses/by/4.0/This 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 license, and indicate if changes were made.The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material.If material is not included in the article’s Creative Commons license 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 license, visit https://creativecommons.org/licenses/by/4.0/.
spellingShingle Clinical Study
McCowan, C
Shearer, J
Donnan, P T
Dewar, J A
Crilly, M
Thompson, A M
Fahey, T P
Cohort study examining tamoxifen adherence and its relationship to mortality in women with breast cancer
title Cohort study examining tamoxifen adherence and its relationship to mortality in women with breast cancer
title_full Cohort study examining tamoxifen adherence and its relationship to mortality in women with breast cancer
title_fullStr Cohort study examining tamoxifen adherence and its relationship to mortality in women with breast cancer
title_full_unstemmed Cohort study examining tamoxifen adherence and its relationship to mortality in women with breast cancer
title_short Cohort study examining tamoxifen adherence and its relationship to mortality in women with breast cancer
title_sort cohort study examining tamoxifen adherence and its relationship to mortality in women with breast cancer
topic Clinical Study
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2600703/
https://www.ncbi.nlm.nih.gov/pubmed/18985046
http://dx.doi.org/10.1038/sj.bjc.6604758
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