Metronomic chemotherapy for non-metastatic triple negative breast cancer: Selection is the key
Descripción del Articulo
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: | , , , |
---|---|
Formato: | artículo |
Fecha de Publicación: | 2017 |
Institución: | Instituto Nacional de Enfermedades Neoplásicas |
Repositorio: | INEN-Institucional |
Lenguaje: | inglés |
OAI Identifier: | oai:repositorio.inen.sld.pe:inen/152 |
Enlace del recurso: | https://repositorio.inen.sld.pe/handle/inen/152 |
Nivel de acceso: | acceso abierto |
Materia: | adjuvant maintenance metronomic chemotherapy neoadjuvant triple negative breast cancer https://purl.org/pe-repo/ocde/ford#3.02.21 |
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Rabanal, ConnieRuiz, RossanaNeciosup, SilviaGomez, Henry L2024-07-01T16:29:08Z2024-07-01T16:29:08Z2017Triple 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.application/pdf10.5306/wjco.v8.i6.437https://repositorio.inen.sld.pe/handle/inen/152engWorld J Clin OncolUSBaishideng Publishing Groupinfo:eu-repo/semantics/openAccessdc.rights.uri: https//creativecomons.org/licenses/by/4.0/adjuvantmaintenancemetronomic chemotherapyneoadjuvanttriple negative breast cancerhttps://purl.org/pe-repo/ocde/ford#3.02.21Metronomic chemotherapy for non-metastatic triple negative breast cancer: Selection is the keyinfo:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionreponame:INEN-Institucionalinstname:Instituto Nacional de Enfermedades Neoplásicasinstacron:INENPublicationORIGINALRabanal 2017.pdfapplication/pdf1027470https://repositorio.inen.sld.pe/bitstreams/7382cec5-6942-4636-a51f-7635f4bd708e/downloadac352ffc139d6771c8434c151ee7850bMD51TEXTRabanal 2017.pdf.txtRabanal 2017.pdf.txtExtracted texttext/plain49227https://repositorio.inen.sld.pe/bitstreams/8ae57c2a-1dd5-42e7-bf85-3af7c4532f51/downloadb04f3c0575047fc788beafbc4f462246MD52THUMBNAILRabanal 2017.pdf.jpgRabanal 2017.pdf.jpgGenerated Thumbnailimage/jpeg6836https://repositorio.inen.sld.pe/bitstreams/bd0373a4-d209-4af8-9be2-dd34eea82209/download33c994e8945e5006c54cc47715692923MD53inen/152oai:repositorio.inen.sld.pe:inen/1522024-10-23 17:40:50.506dc.rights.uri: https//creativecomons.org/licenses/by/4.0/info:eu-repo/semantics/openAccesshttps://repositorio.inen.sld.peRepositorio INENrepositorioinendspace@gmail.com |
dc.title.none.fl_str_mv |
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 |
spellingShingle |
Metronomic chemotherapy for non-metastatic triple negative breast cancer: Selection is the key Rabanal, Connie adjuvant maintenance metronomic chemotherapy neoadjuvant triple negative breast cancer https://purl.org/pe-repo/ocde/ford#3.02.21 |
title_short |
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_sort |
Metronomic chemotherapy for non-metastatic triple negative breast cancer: Selection is the key |
author |
Rabanal, Connie |
author_facet |
Rabanal, Connie Ruiz, Rossana Neciosup, Silvia Gomez, Henry L |
author_role |
author |
author2 |
Ruiz, Rossana Neciosup, Silvia Gomez, Henry L |
author2_role |
author author author |
dc.contributor.author.fl_str_mv |
Rabanal, Connie Ruiz, Rossana Neciosup, Silvia Gomez, Henry L |
dc.subject.none.fl_str_mv |
adjuvant maintenance metronomic chemotherapy neoadjuvant triple negative breast cancer |
topic |
adjuvant maintenance metronomic chemotherapy neoadjuvant triple negative breast cancer https://purl.org/pe-repo/ocde/ford#3.02.21 |
dc.subject.ocde.none.fl_str_mv |
https://purl.org/pe-repo/ocde/ford#3.02.21 |
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. |
publishDate |
2017 |
dc.date.accessioned.none.fl_str_mv |
2024-07-01T16:29:08Z |
dc.date.available.none.fl_str_mv |
2024-07-01T16:29:08Z |
dc.date.issued.fl_str_mv |
2017 |
dc.type.none.fl_str_mv |
info:eu-repo/semantics/article |
dc.type.version.none.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
format |
article |
status_str |
publishedVersion |
dc.identifier.doi.none.fl_str_mv |
10.5306/wjco.v8.i6.437 |
dc.identifier.uri.none.fl_str_mv |
https://repositorio.inen.sld.pe/handle/inen/152 |
identifier_str_mv |
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dc.language.iso.none.fl_str_mv |
eng |
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eng |
dc.relation.ispartof.none.fl_str_mv |
Baishideng Publishing Group |
dc.rights.none.fl_str_mv |
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dc.rights.uri.none.fl_str_mv |
dc.rights.uri: https//creativecomons.org/licenses/by/4.0/ |
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openAccess |
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dc.rights.uri: https//creativecomons.org/licenses/by/4.0/ |
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application/pdf |
dc.publisher.none.fl_str_mv |
World J Clin Oncol |
dc.publisher.country.none.fl_str_mv |
US |
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World J Clin Oncol |
dc.source.none.fl_str_mv |
reponame:INEN-Institucional instname:Instituto Nacional de Enfermedades Neoplásicas instacron:INEN |
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Nota importante:
La información contenida en este registro es de entera responsabilidad de la institución que gestiona el repositorio institucional donde esta contenido este documento o set de datos. El CONCYTEC no se hace responsable por los contenidos (publicaciones y/o datos) accesibles a través del Repositorio Nacional Digital de Ciencia, Tecnología e Innovación de Acceso Abierto (ALICIA).
La información contenida en este registro es de entera responsabilidad de la institución que gestiona el repositorio institucional donde esta contenido este documento o set de datos. El CONCYTEC no se hace responsable por los contenidos (publicaciones y/o datos) accesibles a través del Repositorio Nacional Digital de Ciencia, Tecnología e Innovación de Acceso Abierto (ALICIA).