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Should aromatase inhibitors be used as initial adjuvant treatment or sequenced after tamoxifen?
A number of trials have studied the value of aromatase inhibitors (AIs) for the adjuvant treatment of early hormone-responsive postmenopausal breast cancer. Three different AIs have been used and they have been compared as initial treatment (two trials) or after 2–3 years of tamoxifen (four trials),...
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Formato: | Texto |
Lenguaje: | English |
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Nature Publishing Group
2006
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2361185/ https://www.ncbi.nlm.nih.gov/pubmed/16434989 http://dx.doi.org/10.1038/sj.bjc.6602964 |
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author | Cuzick, J Sasieni, P Howell, A |
author_facet | Cuzick, J Sasieni, P Howell, A |
author_sort | Cuzick, J |
collection | PubMed |
description | A number of trials have studied the value of aromatase inhibitors (AIs) for the adjuvant treatment of early hormone-responsive postmenopausal breast cancer. Three different AIs have been used and they have been compared as initial treatment (two trials) or after 2–3 years of tamoxifen (four trials), in both cases against a standard arm of 5 years of tamoxifen. In addition, two trials have evaluated AIs against no treatment after 5 years of tamoxifen. In all circumstances, the AIs have demonstrated superior efficacy. However, no results are currently available for the key question, that is – is it better to start initially with an AI or use it sequentially after 2 years of tamoxifen? Here, we review the trial results and present two models, which address this issue. The models clearly show that early treatment with an AI is superior to using it after 5 years of tamoxifen. They also favour an upfront strategy to sequencing after 2 years of tamoxifen, but in this case the differences are small and model-dependent. A key question is whether AIs have substantially better efficacy than tamoxifen for ER-positive–PgR-negative tumours, where the data are currently contradictory. A mechanism explaining why greater efficacy might be so is proposed. Further results from ongoing trials will be needed to resolve this issue. |
format | Text |
id | pubmed-2361185 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2006 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-23611852009-09-10 Should aromatase inhibitors be used as initial adjuvant treatment or sequenced after tamoxifen? Cuzick, J Sasieni, P Howell, A Br J Cancer Minireview A number of trials have studied the value of aromatase inhibitors (AIs) for the adjuvant treatment of early hormone-responsive postmenopausal breast cancer. Three different AIs have been used and they have been compared as initial treatment (two trials) or after 2–3 years of tamoxifen (four trials), in both cases against a standard arm of 5 years of tamoxifen. In addition, two trials have evaluated AIs against no treatment after 5 years of tamoxifen. In all circumstances, the AIs have demonstrated superior efficacy. However, no results are currently available for the key question, that is – is it better to start initially with an AI or use it sequentially after 2 years of tamoxifen? Here, we review the trial results and present two models, which address this issue. The models clearly show that early treatment with an AI is superior to using it after 5 years of tamoxifen. They also favour an upfront strategy to sequencing after 2 years of tamoxifen, but in this case the differences are small and model-dependent. A key question is whether AIs have substantially better efficacy than tamoxifen for ER-positive–PgR-negative tumours, where the data are currently contradictory. A mechanism explaining why greater efficacy might be so is proposed. Further results from ongoing trials will be needed to resolve this issue. Nature Publishing Group 2006-02-27 2006-01-24 /pmc/articles/PMC2361185/ /pubmed/16434989 http://dx.doi.org/10.1038/sj.bjc.6602964 Text en Copyright © 2006 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 | Minireview Cuzick, J Sasieni, P Howell, A Should aromatase inhibitors be used as initial adjuvant treatment or sequenced after tamoxifen? |
title | Should aromatase inhibitors be used as initial adjuvant treatment or sequenced after tamoxifen? |
title_full | Should aromatase inhibitors be used as initial adjuvant treatment or sequenced after tamoxifen? |
title_fullStr | Should aromatase inhibitors be used as initial adjuvant treatment or sequenced after tamoxifen? |
title_full_unstemmed | Should aromatase inhibitors be used as initial adjuvant treatment or sequenced after tamoxifen? |
title_short | Should aromatase inhibitors be used as initial adjuvant treatment or sequenced after tamoxifen? |
title_sort | should aromatase inhibitors be used as initial adjuvant treatment or sequenced after tamoxifen? |
topic | Minireview |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2361185/ https://www.ncbi.nlm.nih.gov/pubmed/16434989 http://dx.doi.org/10.1038/sj.bjc.6602964 |
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