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Metronomic chemotherapy for non-metastatic triple negative breast cancer: Selection is the key
Triple negative breast cancer (TNBC) accounts for 15%-20% of all breast cancer, and is still defined as what it is not. Currently, TNBC is the only type of breast cancer for which there are no approved targeted therapies and maximum tolerated dose chemotherapy with taxanes and anthracycline-containi...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Baishideng Publishing Group Inc
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5740099/ https://www.ncbi.nlm.nih.gov/pubmed/29291168 http://dx.doi.org/10.5306/wjco.v8.i6.437 |
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author | Rabanal, Connie Ruiz, Rossana Neciosup, Silvia Gomez, Henry |
author_facet | Rabanal, Connie Ruiz, Rossana Neciosup, Silvia Gomez, Henry |
author_sort | Rabanal, Connie |
collection | PubMed |
description | Triple negative breast cancer (TNBC) accounts for 15%-20% of all breast cancer, and is still defined as what it is not. Currently, TNBC is the only type of breast cancer for which there are no approved targeted therapies and maximum tolerated dose chemotherapy with taxanes and anthracycline-containing regimens is still the standard of care in both the neoadjuvant and adjuvant settings. In the last years, metronomic chemotherapy (MC) is being explored as an alternative to improve outcomes in TNBC. In the neoadjuvant setting, purely metronomic and hybrid approaches have been developed with the objective of increasing complete pathologic response (pCR) and prolonging disease free survival. These regimens proved to be very effective achieving pCR rates between 47%-60%, but at the cost of great toxicity. In the adjuvant setting, MC is used to intensify adjuvant chemotherapy and, more promisingly, as maintenance therapy for high-risk patients, especially those with no pCR after neoadjuvant chemotherapy. Considering the dismal prognosis of TNBC, any strategy that potentially improves outcomes, specially being the oral agents broadly available and inexpensive, should be considered and certainly warrants further exploration. Finally, the benefit of MC needs to be validated in properly designed clinical trials were the selection of the population is the key. |
format | Online Article Text |
id | pubmed-5740099 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Baishideng Publishing Group Inc |
record_format | MEDLINE/PubMed |
spelling | pubmed-57400992017-12-31 Metronomic chemotherapy for non-metastatic triple negative breast cancer: Selection is the key Rabanal, Connie Ruiz, Rossana Neciosup, Silvia Gomez, Henry World J Clin Oncol Minireviews Triple negative breast cancer (TNBC) accounts for 15%-20% of all breast cancer, and is still defined as what it is not. Currently, TNBC is the only type of breast cancer for which there are no approved targeted therapies and maximum tolerated dose chemotherapy with taxanes and anthracycline-containing regimens is still the standard of care in both the neoadjuvant and adjuvant settings. In the last years, metronomic chemotherapy (MC) is being explored as an alternative to improve outcomes in TNBC. In the neoadjuvant setting, purely metronomic and hybrid approaches have been developed with the objective of increasing complete pathologic response (pCR) and prolonging disease free survival. These regimens proved to be very effective achieving pCR rates between 47%-60%, but at the cost of great toxicity. In the adjuvant setting, MC is used to intensify adjuvant chemotherapy and, more promisingly, as maintenance therapy for high-risk patients, especially those with no pCR after neoadjuvant chemotherapy. Considering the dismal prognosis of TNBC, any strategy that potentially improves outcomes, specially being the oral agents broadly available and inexpensive, should be considered and certainly warrants further exploration. Finally, the benefit of MC needs to be validated in properly designed clinical trials were the selection of the population is the key. Baishideng Publishing Group Inc 2017-12-10 2017-12-10 /pmc/articles/PMC5740099/ /pubmed/29291168 http://dx.doi.org/10.5306/wjco.v8.i6.437 Text en ©The Author(s) 2017. Published by Baishideng Publishing Group Inc. All rights reserved. http://creativecommons.org/licenses/by-nc/4.0/ Open-Access: This article is an open-access article which was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/ |
spellingShingle | Minireviews Rabanal, Connie Ruiz, Rossana Neciosup, Silvia Gomez, Henry Metronomic chemotherapy for non-metastatic triple negative breast cancer: Selection is the key |
title | Metronomic chemotherapy for non-metastatic triple negative breast cancer: Selection is the key |
title_full | Metronomic chemotherapy for non-metastatic triple negative breast cancer: Selection is the key |
title_fullStr | Metronomic chemotherapy for non-metastatic triple negative breast cancer: Selection is the key |
title_full_unstemmed | Metronomic chemotherapy for non-metastatic triple negative breast cancer: Selection is the key |
title_short | Metronomic chemotherapy for non-metastatic triple negative breast cancer: Selection is the key |
title_sort | metronomic chemotherapy for non-metastatic triple negative breast cancer: selection is the key |
topic | Minireviews |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5740099/ https://www.ncbi.nlm.nih.gov/pubmed/29291168 http://dx.doi.org/10.5306/wjco.v8.i6.437 |
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