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Adjuvant endocrine therapy for postmenopausal breast cancer in the era of aromatase inhibitors: an update
There is overwhelming evidence that optimal adjuvant endocrine therapy for hormone sensitive breast cancer in postmenopausal women should include a third generation aromatase inhibitor (AI). On current evidence, adjuvant anstrozole or letrozole should be used upfront in such patients especially in t...
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2006
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1586206/ https://www.ncbi.nlm.nih.gov/pubmed/16981992 http://dx.doi.org/10.1186/1477-7800-3-31 |
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author | Mokbel, Ramia Karat, Isabella Mokbel, Kefah |
author_facet | Mokbel, Ramia Karat, Isabella Mokbel, Kefah |
author_sort | Mokbel, Ramia |
collection | PubMed |
description | There is overwhelming evidence that optimal adjuvant endocrine therapy for hormone sensitive breast cancer in postmenopausal women should include a third generation aromatase inhibitor (AI). On current evidence, adjuvant anstrozole or letrozole should be used upfront in such patients especially in those with high risk disease (node positive and/or tumours > 2 cm). The sequential approach of tamoxifen for 2–3 years followed by exemestane or anastrozole for 2–3 years is a reasonable alternative to 5 years of AI monotherapy in patients with low risk disease (node negative and tumour smaller than 2 cm) especially if the tumour is positive for estrogen and progesterone receptors. Node-positive patients completing 5 years of adjuvant tamoxifen should be offered letrozole for up 48 months. Further research is required to establish the long-term cardiovascular safety of AIs especially that of letrozole and exmestane, the optimal AI to use, duration of AI therapy and whether monotherapy with an AI for 5 years is superior to sequencing an AI after 2–3 years of tamoxifen. The bone mineral density (BMD) should be measured at baseline and monitored during therapy in women being treated with AIs. Anti-osteoporosis agents should such as bisphosphonates should be considered in patients at high risk of bone fractures. |
format | Text |
id | pubmed-1586206 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2006 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-15862062006-10-03 Adjuvant endocrine therapy for postmenopausal breast cancer in the era of aromatase inhibitors: an update Mokbel, Ramia Karat, Isabella Mokbel, Kefah Int Semin Surg Oncol Editorial There is overwhelming evidence that optimal adjuvant endocrine therapy for hormone sensitive breast cancer in postmenopausal women should include a third generation aromatase inhibitor (AI). On current evidence, adjuvant anstrozole or letrozole should be used upfront in such patients especially in those with high risk disease (node positive and/or tumours > 2 cm). The sequential approach of tamoxifen for 2–3 years followed by exemestane or anastrozole for 2–3 years is a reasonable alternative to 5 years of AI monotherapy in patients with low risk disease (node negative and tumour smaller than 2 cm) especially if the tumour is positive for estrogen and progesterone receptors. Node-positive patients completing 5 years of adjuvant tamoxifen should be offered letrozole for up 48 months. Further research is required to establish the long-term cardiovascular safety of AIs especially that of letrozole and exmestane, the optimal AI to use, duration of AI therapy and whether monotherapy with an AI for 5 years is superior to sequencing an AI after 2–3 years of tamoxifen. The bone mineral density (BMD) should be measured at baseline and monitored during therapy in women being treated with AIs. Anti-osteoporosis agents should such as bisphosphonates should be considered in patients at high risk of bone fractures. BioMed Central 2006-09-18 /pmc/articles/PMC1586206/ /pubmed/16981992 http://dx.doi.org/10.1186/1477-7800-3-31 Text en Copyright © 2006 Mokbel et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Editorial Mokbel, Ramia Karat, Isabella Mokbel, Kefah Adjuvant endocrine therapy for postmenopausal breast cancer in the era of aromatase inhibitors: an update |
title | Adjuvant endocrine therapy for postmenopausal breast cancer in the era of aromatase inhibitors: an update |
title_full | Adjuvant endocrine therapy for postmenopausal breast cancer in the era of aromatase inhibitors: an update |
title_fullStr | Adjuvant endocrine therapy for postmenopausal breast cancer in the era of aromatase inhibitors: an update |
title_full_unstemmed | Adjuvant endocrine therapy for postmenopausal breast cancer in the era of aromatase inhibitors: an update |
title_short | Adjuvant endocrine therapy for postmenopausal breast cancer in the era of aromatase inhibitors: an update |
title_sort | adjuvant endocrine therapy for postmenopausal breast cancer in the era of aromatase inhibitors: an update |
topic | Editorial |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1586206/ https://www.ncbi.nlm.nih.gov/pubmed/16981992 http://dx.doi.org/10.1186/1477-7800-3-31 |
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