Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Mokbel, Ramia, Karat, Isabella, Mokbel, Kefah
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2006
Materias:
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
_version_ 1782130353431904256
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
work_keys_str_mv AT mokbelramia adjuvantendocrinetherapyforpostmenopausalbreastcancerintheeraofaromataseinhibitorsanupdate
AT karatisabella adjuvantendocrinetherapyforpostmenopausalbreastcancerintheeraofaromataseinhibitorsanupdate
AT mokbelkefah adjuvantendocrinetherapyforpostmenopausalbreastcancerintheeraofaromataseinhibitorsanupdate