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Advancements in Human Breast Cancer Targeted Therapy and Immunotherapy

Human breast cancer treatment regimens have evolved greatly due to the significant advances in understanding the molecular mechanisms and pathways of the common subtypes of breast cancer. In this review, we discuss recent progress in breast cancer targeted therapy and immunotherapy as well as ongoin...

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Autores principales: Bou-Dargham, Mayassa J., Draughon, Sophia, Cantrell, Vance, Khamis, Zahraa I., Sang, Qing-Xiang Amy
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Ivyspring International Publisher 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8558657/
https://www.ncbi.nlm.nih.gov/pubmed/34729098
http://dx.doi.org/10.7150/jca.64205
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author Bou-Dargham, Mayassa J.
Draughon, Sophia
Cantrell, Vance
Khamis, Zahraa I.
Sang, Qing-Xiang Amy
author_facet Bou-Dargham, Mayassa J.
Draughon, Sophia
Cantrell, Vance
Khamis, Zahraa I.
Sang, Qing-Xiang Amy
author_sort Bou-Dargham, Mayassa J.
collection PubMed
description Human breast cancer treatment regimens have evolved greatly due to the significant advances in understanding the molecular mechanisms and pathways of the common subtypes of breast cancer. In this review, we discuss recent progress in breast cancer targeted therapy and immunotherapy as well as ongoing clinical trials. We also highlight the potential of combination therapies and personalized approaches to improve clinical outcomes. Targeted therapies have surpassed the hormone receptors and the human epidermal growth factor receptor 2 (HER2) to include many other molecules in targetable pathways such as the epidermal growth factor receptor (EGFR), poly (adenosine diphosphate-ribose) polymerase (PARP), and cyclin-dependent kinase 4/6 (CDK4/6). However, resistance to targeted therapy persists, underpinning the need for more efficacious therapies. Immunotherapy is considered a milestone in breast cancer treatments, including the engineered immune cells (CAR-T cell therapy) to better target the tumor cells, vaccines to stimulate the patient's immune system against tumor antigens, and checkpoint inhibitors (PD-1, PD-L1, and CTLA4) to block molecules that mediate immune inhibition. Targeted therapies and immunotherapy tested in breast cancer clinical trials are discussed here, with special emphasis on combinatorial approaches which are believed to maximize treatment efficacy and enhance patient survival.
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spelling pubmed-85586572021-11-01 Advancements in Human Breast Cancer Targeted Therapy and Immunotherapy Bou-Dargham, Mayassa J. Draughon, Sophia Cantrell, Vance Khamis, Zahraa I. Sang, Qing-Xiang Amy J Cancer Review Human breast cancer treatment regimens have evolved greatly due to the significant advances in understanding the molecular mechanisms and pathways of the common subtypes of breast cancer. In this review, we discuss recent progress in breast cancer targeted therapy and immunotherapy as well as ongoing clinical trials. We also highlight the potential of combination therapies and personalized approaches to improve clinical outcomes. Targeted therapies have surpassed the hormone receptors and the human epidermal growth factor receptor 2 (HER2) to include many other molecules in targetable pathways such as the epidermal growth factor receptor (EGFR), poly (adenosine diphosphate-ribose) polymerase (PARP), and cyclin-dependent kinase 4/6 (CDK4/6). However, resistance to targeted therapy persists, underpinning the need for more efficacious therapies. Immunotherapy is considered a milestone in breast cancer treatments, including the engineered immune cells (CAR-T cell therapy) to better target the tumor cells, vaccines to stimulate the patient's immune system against tumor antigens, and checkpoint inhibitors (PD-1, PD-L1, and CTLA4) to block molecules that mediate immune inhibition. Targeted therapies and immunotherapy tested in breast cancer clinical trials are discussed here, with special emphasis on combinatorial approaches which are believed to maximize treatment efficacy and enhance patient survival. Ivyspring International Publisher 2021-10-11 /pmc/articles/PMC8558657/ /pubmed/34729098 http://dx.doi.org/10.7150/jca.64205 Text en © The author(s) https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/). See http://ivyspring.com/terms for full terms and conditions.
spellingShingle Review
Bou-Dargham, Mayassa J.
Draughon, Sophia
Cantrell, Vance
Khamis, Zahraa I.
Sang, Qing-Xiang Amy
Advancements in Human Breast Cancer Targeted Therapy and Immunotherapy
title Advancements in Human Breast Cancer Targeted Therapy and Immunotherapy
title_full Advancements in Human Breast Cancer Targeted Therapy and Immunotherapy
title_fullStr Advancements in Human Breast Cancer Targeted Therapy and Immunotherapy
title_full_unstemmed Advancements in Human Breast Cancer Targeted Therapy and Immunotherapy
title_short Advancements in Human Breast Cancer Targeted Therapy and Immunotherapy
title_sort advancements in human breast cancer targeted therapy and immunotherapy
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8558657/
https://www.ncbi.nlm.nih.gov/pubmed/34729098
http://dx.doi.org/10.7150/jca.64205
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