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Anti-HER2 therapy in metastatic breast cancer: many choices and future directions

Metastatic HER2 + breast cancer is an expanding area of drug development and research, with three new drugs approved in 2020 alone. While first-line therapy is well-established for metastatic HER2 + breast cancer, the standard of care for second-line therapy will likely be changing soon based on the...

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Autores principales: Wynn, Carrie S., Tang, Shou-Ching
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8924093/
https://www.ncbi.nlm.nih.gov/pubmed/35142964
http://dx.doi.org/10.1007/s10555-022-10021-x
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author Wynn, Carrie S.
Tang, Shou-Ching
author_facet Wynn, Carrie S.
Tang, Shou-Ching
author_sort Wynn, Carrie S.
collection PubMed
description Metastatic HER2 + breast cancer is an expanding area of drug development and research, with three new drugs approved in 2020 alone. While first-line therapy is well-established for metastatic HER2 + breast cancer, the standard of care for second-line therapy will likely be changing soon based on the results of the DESTINY-Breast03 trial. In the third-line setting, many options are available. Considerations in choosing between regimens in the third-line include resistance to trastuzumab, the presence of brain metastases, and tolerability. High rates of resistance exist in this setting particularly due to expression of p95, a truncated form of HER2 that constitutively activates downstream signaling pathways. We suggest a tyrosine kinase inhibitor (TKI)-based regimen because of the activity of TKIs in brain metastases and in p95-expressing tumors. Attempts to overcome resistance to anti-HER2 therapies with PI3K inhibitors, mTOR inhibitors, and CDK 4/6 inhibitors are an active area of research. In the future, biomarkers are needed to help predict which therapies patients may benefit from the most. We review the many new drugs in development, including those with novel mechanisms of action.
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spelling pubmed-89240932022-03-17 Anti-HER2 therapy in metastatic breast cancer: many choices and future directions Wynn, Carrie S. Tang, Shou-Ching Cancer Metastasis Rev Clinical Metastatic HER2 + breast cancer is an expanding area of drug development and research, with three new drugs approved in 2020 alone. While first-line therapy is well-established for metastatic HER2 + breast cancer, the standard of care for second-line therapy will likely be changing soon based on the results of the DESTINY-Breast03 trial. In the third-line setting, many options are available. Considerations in choosing between regimens in the third-line include resistance to trastuzumab, the presence of brain metastases, and tolerability. High rates of resistance exist in this setting particularly due to expression of p95, a truncated form of HER2 that constitutively activates downstream signaling pathways. We suggest a tyrosine kinase inhibitor (TKI)-based regimen because of the activity of TKIs in brain metastases and in p95-expressing tumors. Attempts to overcome resistance to anti-HER2 therapies with PI3K inhibitors, mTOR inhibitors, and CDK 4/6 inhibitors are an active area of research. In the future, biomarkers are needed to help predict which therapies patients may benefit from the most. We review the many new drugs in development, including those with novel mechanisms of action. Springer US 2022-02-10 2022 /pmc/articles/PMC8924093/ /pubmed/35142964 http://dx.doi.org/10.1007/s10555-022-10021-x Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Clinical
Wynn, Carrie S.
Tang, Shou-Ching
Anti-HER2 therapy in metastatic breast cancer: many choices and future directions
title Anti-HER2 therapy in metastatic breast cancer: many choices and future directions
title_full Anti-HER2 therapy in metastatic breast cancer: many choices and future directions
title_fullStr Anti-HER2 therapy in metastatic breast cancer: many choices and future directions
title_full_unstemmed Anti-HER2 therapy in metastatic breast cancer: many choices and future directions
title_short Anti-HER2 therapy in metastatic breast cancer: many choices and future directions
title_sort anti-her2 therapy in metastatic breast cancer: many choices and future directions
topic Clinical
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8924093/
https://www.ncbi.nlm.nih.gov/pubmed/35142964
http://dx.doi.org/10.1007/s10555-022-10021-x
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