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Neoadjuvant treatments in triple-negative breast cancer patients: where we are now and where we are going
Triple-negative breast cancer (TNBC) remains the poorest-prognosis breast cancer (BC) subtype. Gene expression profiling has identified at least six different triple-negative subtypes with different biology and sensitivity to therapies. The heterogeneous nature of TN tumors may justify the difficult...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5772398/ https://www.ncbi.nlm.nih.gov/pubmed/29391830 http://dx.doi.org/10.2147/CMAR.S146658 |
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author | Omarini, Claudia Guaitoli, Giorgia Pipitone, Stefania Moscetti, Luca Cortesi, Laura Cascinu, Stefano Piacentini, Federico |
author_facet | Omarini, Claudia Guaitoli, Giorgia Pipitone, Stefania Moscetti, Luca Cortesi, Laura Cascinu, Stefano Piacentini, Federico |
author_sort | Omarini, Claudia |
collection | PubMed |
description | Triple-negative breast cancer (TNBC) remains the poorest-prognosis breast cancer (BC) subtype. Gene expression profiling has identified at least six different triple-negative subtypes with different biology and sensitivity to therapies. The heterogeneous nature of TN tumors may justify the difficulty in treating this BC subtype. Several targeted agents have been investigated in clinical trials without demonstrating a clear survival benefit. Therefore, systemic chemotherapy remains the cornerstone of current clinical practice. Improving the knowledge of tumor biology is mandatory for patient management. In stages II and III, neoadjuvant systemic treatment is an effective option of care. The achievement of a pathological complete response represents an optimal surrogate for survival outcome as well as a test for tumor drug sensitivity. In this review, we provide a brief description of the main predictive biomarkers for tumor response to systemic treatment. Moreover, we review the treatment strategies investigated for TNBCs in neoadjuvant settings focusing on experimental drugs such as immunotherapy and poly [ADP-ribose] polymerase inhibitors that hold promise in the treatment of this aggressive disease. Therefore, the management of TNBC represents an urgent, current, unmet need in daily clinical practice. A key recommendation is to design biology-driven clinical trials wherein TNBC patients may be treated on the basis of tumor molecular profile. |
format | Online Article Text |
id | pubmed-5772398 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-57723982018-02-01 Neoadjuvant treatments in triple-negative breast cancer patients: where we are now and where we are going Omarini, Claudia Guaitoli, Giorgia Pipitone, Stefania Moscetti, Luca Cortesi, Laura Cascinu, Stefano Piacentini, Federico Cancer Manag Res Review Triple-negative breast cancer (TNBC) remains the poorest-prognosis breast cancer (BC) subtype. Gene expression profiling has identified at least six different triple-negative subtypes with different biology and sensitivity to therapies. The heterogeneous nature of TN tumors may justify the difficulty in treating this BC subtype. Several targeted agents have been investigated in clinical trials without demonstrating a clear survival benefit. Therefore, systemic chemotherapy remains the cornerstone of current clinical practice. Improving the knowledge of tumor biology is mandatory for patient management. In stages II and III, neoadjuvant systemic treatment is an effective option of care. The achievement of a pathological complete response represents an optimal surrogate for survival outcome as well as a test for tumor drug sensitivity. In this review, we provide a brief description of the main predictive biomarkers for tumor response to systemic treatment. Moreover, we review the treatment strategies investigated for TNBCs in neoadjuvant settings focusing on experimental drugs such as immunotherapy and poly [ADP-ribose] polymerase inhibitors that hold promise in the treatment of this aggressive disease. Therefore, the management of TNBC represents an urgent, current, unmet need in daily clinical practice. A key recommendation is to design biology-driven clinical trials wherein TNBC patients may be treated on the basis of tumor molecular profile. Dove Medical Press 2018-01-15 /pmc/articles/PMC5772398/ /pubmed/29391830 http://dx.doi.org/10.2147/CMAR.S146658 Text en © 2018 Omarini et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. |
spellingShingle | Review Omarini, Claudia Guaitoli, Giorgia Pipitone, Stefania Moscetti, Luca Cortesi, Laura Cascinu, Stefano Piacentini, Federico Neoadjuvant treatments in triple-negative breast cancer patients: where we are now and where we are going |
title | Neoadjuvant treatments in triple-negative breast cancer patients: where we are now and where we are going |
title_full | Neoadjuvant treatments in triple-negative breast cancer patients: where we are now and where we are going |
title_fullStr | Neoadjuvant treatments in triple-negative breast cancer patients: where we are now and where we are going |
title_full_unstemmed | Neoadjuvant treatments in triple-negative breast cancer patients: where we are now and where we are going |
title_short | Neoadjuvant treatments in triple-negative breast cancer patients: where we are now and where we are going |
title_sort | neoadjuvant treatments in triple-negative breast cancer patients: where we are now and where we are going |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5772398/ https://www.ncbi.nlm.nih.gov/pubmed/29391830 http://dx.doi.org/10.2147/CMAR.S146658 |
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