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Aromatase inhibitor treatment for breast cancer: short-term effect on bone health
AIM OF THIS STUDY: Aim of this study was to examine the effects of aromatase inhibitors (AIs), which are used in every phase of breast cancer treatment, on the bone mineral density (BMD) of patients with early-stage breast cancer. MATERIAL AND METHODS: Menopausal female patients who were diagnosed w...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Termedia Publishing House
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4709393/ https://www.ncbi.nlm.nih.gov/pubmed/26793021 http://dx.doi.org/10.5114/wo.2014.45305 |
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author | Erbağ, Gökhan Uygun, Kazım Binnetoğlu, Emine Korkmaz, Ayşe Nurdan Aşık, Mehmet Şen, Hacer Güneş, Fahri Eroğlu, Mustafa Gökmen, Ferhat Temiz, Süleyman |
author_facet | Erbağ, Gökhan Uygun, Kazım Binnetoğlu, Emine Korkmaz, Ayşe Nurdan Aşık, Mehmet Şen, Hacer Güneş, Fahri Eroğlu, Mustafa Gökmen, Ferhat Temiz, Süleyman |
author_sort | Erbağ, Gökhan |
collection | PubMed |
description | AIM OF THIS STUDY: Aim of this study was to examine the effects of aromatase inhibitors (AIs), which are used in every phase of breast cancer treatment, on the bone mineral density (BMD) of patients with early-stage breast cancer. MATERIAL AND METHODS: Menopausal female patients who were diagnosed with stages 1–3 breast cancer and who were planned for anastrazole or letrozole as adjuvant therapy were examined. After the patients’ BMD was measured, 45 patients without osteoporosis were included in the study. Six months after AI therapy started, the patients’ BMD was measured again. RESULTS: In this study, we tried to show that there was a statistical difference in the BMD of 45 patients before and 6 months after treatment. Among all measurements (femur and lumbar T-scores), the femur Z-score (p = 0.52) was the only score that was not statistically significant. Statistical significance (p < 0.01) was detected in comparative analysis of the other measurements. According to this analysis, a significant loss of BMD was seen even in the first six months after AI treatment was introduced. CONCLUSIONS: Female patients with breast cancer are at higher risk for bone loss and fractures than healthy women. In this study, we showed the negative effects on BMD of aromatase inhibitor therapy, one of the main contributions to osteoporosis in women with breast cancer. This study is the first to quantify the short-term effect of AI treatment on BMD in postmenopausal women with breast cancer. |
format | Online Article Text |
id | pubmed-4709393 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Termedia Publishing House |
record_format | MEDLINE/PubMed |
spelling | pubmed-47093932016-01-20 Aromatase inhibitor treatment for breast cancer: short-term effect on bone health Erbağ, Gökhan Uygun, Kazım Binnetoğlu, Emine Korkmaz, Ayşe Nurdan Aşık, Mehmet Şen, Hacer Güneş, Fahri Eroğlu, Mustafa Gökmen, Ferhat Temiz, Süleyman Contemp Oncol (Pozn) Original Paper AIM OF THIS STUDY: Aim of this study was to examine the effects of aromatase inhibitors (AIs), which are used in every phase of breast cancer treatment, on the bone mineral density (BMD) of patients with early-stage breast cancer. MATERIAL AND METHODS: Menopausal female patients who were diagnosed with stages 1–3 breast cancer and who were planned for anastrazole or letrozole as adjuvant therapy were examined. After the patients’ BMD was measured, 45 patients without osteoporosis were included in the study. Six months after AI therapy started, the patients’ BMD was measured again. RESULTS: In this study, we tried to show that there was a statistical difference in the BMD of 45 patients before and 6 months after treatment. Among all measurements (femur and lumbar T-scores), the femur Z-score (p = 0.52) was the only score that was not statistically significant. Statistical significance (p < 0.01) was detected in comparative analysis of the other measurements. According to this analysis, a significant loss of BMD was seen even in the first six months after AI treatment was introduced. CONCLUSIONS: Female patients with breast cancer are at higher risk for bone loss and fractures than healthy women. In this study, we showed the negative effects on BMD of aromatase inhibitor therapy, one of the main contributions to osteoporosis in women with breast cancer. This study is the first to quantify the short-term effect of AI treatment on BMD in postmenopausal women with breast cancer. Termedia Publishing House 2015-08-07 2015 /pmc/articles/PMC4709393/ /pubmed/26793021 http://dx.doi.org/10.5114/wo.2014.45305 Text en Copyright © 2015 Termedia http://creativecommons.org/licenses/by-nc-sa/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0) License, allowing third parties to copy and redistribute the material in any medium or format and to remix, transform, and build upon the material, provided the original work is properly cited and states its license. |
spellingShingle | Original Paper Erbağ, Gökhan Uygun, Kazım Binnetoğlu, Emine Korkmaz, Ayşe Nurdan Aşık, Mehmet Şen, Hacer Güneş, Fahri Eroğlu, Mustafa Gökmen, Ferhat Temiz, Süleyman Aromatase inhibitor treatment for breast cancer: short-term effect on bone health |
title | Aromatase inhibitor treatment for breast cancer: short-term effect on bone health |
title_full | Aromatase inhibitor treatment for breast cancer: short-term effect on bone health |
title_fullStr | Aromatase inhibitor treatment for breast cancer: short-term effect on bone health |
title_full_unstemmed | Aromatase inhibitor treatment for breast cancer: short-term effect on bone health |
title_short | Aromatase inhibitor treatment for breast cancer: short-term effect on bone health |
title_sort | aromatase inhibitor treatment for breast cancer: short-term effect on bone health |
topic | Original Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4709393/ https://www.ncbi.nlm.nih.gov/pubmed/26793021 http://dx.doi.org/10.5114/wo.2014.45305 |
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