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Approach to the Triple Negative Breast Cancer in New Drugs Area

Triple negative breast cancers (TNBCs) are associated with aggressive course, higher rates of visceral and central nervous system metastases and lower survival rate than hormone receptor positive. Once metastasis has occurred, a median survival was approximately one year. Currently, chemotherapy in...

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Autor principal: Mirzania, Mehrzad
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Tehran University of Medical Sciences, Hematology-Oncology and Stem Cell Transplantation Research Center 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4888149/
https://www.ncbi.nlm.nih.gov/pubmed/27252813
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author Mirzania, Mehrzad
author_facet Mirzania, Mehrzad
author_sort Mirzania, Mehrzad
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description Triple negative breast cancers (TNBCs) are associated with aggressive course, higher rates of visceral and central nervous system metastases and lower survival rate than hormone receptor positive. Once metastasis has occurred, a median survival was approximately one year. Currently, chemotherapy in TNBC is similar to other HER2- negative breast cancers but in the near future, it will revolutionize. TNBCs are quite heterogeneous based on biomarkers and genetic variations. The series of new drugs have been tried; in this article, platinum, anti-epigenetic drugs, PARP inhibitors, epidermal growth factor receptor inhibitor, Src family kinase inhibitor, anti androgen, glycoprotein Non-metastatic melanoma B (gpNMB) antibody, LHRH conjugated to cytotoxic drugs and inhibition of the PI3K/AKT/mTOR pathway will be explained. What is the optimal therapy for TNBC patients? It is still not clear but it seems that the road map according to biological and genetic markers is taking shape.
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spelling pubmed-48881492016-06-01 Approach to the Triple Negative Breast Cancer in New Drugs Area Mirzania, Mehrzad Int J Hematol Oncol Stem Cell Res Review Article Triple negative breast cancers (TNBCs) are associated with aggressive course, higher rates of visceral and central nervous system metastases and lower survival rate than hormone receptor positive. Once metastasis has occurred, a median survival was approximately one year. Currently, chemotherapy in TNBC is similar to other HER2- negative breast cancers but in the near future, it will revolutionize. TNBCs are quite heterogeneous based on biomarkers and genetic variations. The series of new drugs have been tried; in this article, platinum, anti-epigenetic drugs, PARP inhibitors, epidermal growth factor receptor inhibitor, Src family kinase inhibitor, anti androgen, glycoprotein Non-metastatic melanoma B (gpNMB) antibody, LHRH conjugated to cytotoxic drugs and inhibition of the PI3K/AKT/mTOR pathway will be explained. What is the optimal therapy for TNBC patients? It is still not clear but it seems that the road map according to biological and genetic markers is taking shape. Tehran University of Medical Sciences, Hematology-Oncology and Stem Cell Transplantation Research Center 2016-04-01 /pmc/articles/PMC4888149/ /pubmed/27252813 Text en Copyright : © International Journal of Hematology-Oncology and Stem Cell Research & Tehran University of Medical Sciences This is an Open Access article distributed under the terms of the Creative Commons Attribution License, (http://creativecommons.org/licenses/by/3.0/) which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Mirzania, Mehrzad
Approach to the Triple Negative Breast Cancer in New Drugs Area
title Approach to the Triple Negative Breast Cancer in New Drugs Area
title_full Approach to the Triple Negative Breast Cancer in New Drugs Area
title_fullStr Approach to the Triple Negative Breast Cancer in New Drugs Area
title_full_unstemmed Approach to the Triple Negative Breast Cancer in New Drugs Area
title_short Approach to the Triple Negative Breast Cancer in New Drugs Area
title_sort approach to the triple negative breast cancer in new drugs area
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4888149/
https://www.ncbi.nlm.nih.gov/pubmed/27252813
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