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Safety of adjuvant endocrine therapies in hormone receptor–positive early breast cancer

Postmenopausal patients with hormone-sensitive early breast cancer are typically treated with adjuvant endocrine therapy, which significantly reduces the risk of recurrence. Because treatment is of a long duration, side effects from adjuvant therapy can be problematic. The aromatase inhibitors (AIS)...

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Autores principales: Sehdev, S., Martin, G., Sideris, L., Lam, W., Brisson, S.
Formato: Texto
Lenguaje:English
Publicado: Multimed Inc. 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2722047/
https://www.ncbi.nlm.nih.gov/pubmed/19672417
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author Sehdev, S.
Martin, G.
Sideris, L.
Lam, W.
Brisson, S.
author_facet Sehdev, S.
Martin, G.
Sideris, L.
Lam, W.
Brisson, S.
author_sort Sehdev, S.
collection PubMed
description Postmenopausal patients with hormone-sensitive early breast cancer are typically treated with adjuvant endocrine therapy, which significantly reduces the risk of recurrence. Because treatment is of a long duration, side effects from adjuvant therapy can be problematic. The aromatase inhibitors (AIS) are replacing tamoxifen as first-line treatment agents for early breast cancer. Here, we present the side-effect data associated with AIS in relation to bone, gynecologic, and cardiovascular health and to arthralgia and myalgia. Although AIS have been shown to decrease bone density, increase arthralgia, and affect vaginal health, these adverse events are usually manageable, and several strategies can be followed to improve quality of life in women on AI treatment. To optimize adherence to therapy. It is important that these issues are addressed so that women can benefit from treatment.
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spelling pubmed-27220472009-08-11 Safety of adjuvant endocrine therapies in hormone receptor–positive early breast cancer Sehdev, S. Martin, G. Sideris, L. Lam, W. Brisson, S. Curr Oncol Medical Oncology Postmenopausal patients with hormone-sensitive early breast cancer are typically treated with adjuvant endocrine therapy, which significantly reduces the risk of recurrence. Because treatment is of a long duration, side effects from adjuvant therapy can be problematic. The aromatase inhibitors (AIS) are replacing tamoxifen as first-line treatment agents for early breast cancer. Here, we present the side-effect data associated with AIS in relation to bone, gynecologic, and cardiovascular health and to arthralgia and myalgia. Although AIS have been shown to decrease bone density, increase arthralgia, and affect vaginal health, these adverse events are usually manageable, and several strategies can be followed to improve quality of life in women on AI treatment. To optimize adherence to therapy. It is important that these issues are addressed so that women can benefit from treatment. Multimed Inc. 2009-07 /pmc/articles/PMC2722047/ /pubmed/19672417 Text en 2009 Multimed Inc. http://creativecommons.org/licenses/by/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Medical Oncology
Sehdev, S.
Martin, G.
Sideris, L.
Lam, W.
Brisson, S.
Safety of adjuvant endocrine therapies in hormone receptor–positive early breast cancer
title Safety of adjuvant endocrine therapies in hormone receptor–positive early breast cancer
title_full Safety of adjuvant endocrine therapies in hormone receptor–positive early breast cancer
title_fullStr Safety of adjuvant endocrine therapies in hormone receptor–positive early breast cancer
title_full_unstemmed Safety of adjuvant endocrine therapies in hormone receptor–positive early breast cancer
title_short Safety of adjuvant endocrine therapies in hormone receptor–positive early breast cancer
title_sort safety of adjuvant endocrine therapies in hormone receptor–positive early breast cancer
topic Medical Oncology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2722047/
https://www.ncbi.nlm.nih.gov/pubmed/19672417
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