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...

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Detalles Bibliográficos
Autores: Rabanal, Connie, Ruiz, Rossana, Neciosup, Silvia, Gomez, Henry L
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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spelling 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
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