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Biosimilars for breast cancer: a review of HER2-targeted antibodies in the United States

The utilization of trastuzumab biosimilar medications is of particular interest in HER2-positive breast cancer as these drugs have the potential for cost savings and increased utilization/access to HER2 targeted therapy in both early stage and metastatic HER2-positive breast cancers. Five trastuzuma...

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Detalles Bibliográficos
Autores principales: Miller, Emily M., Schwartzberg, Lee S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6859678/
https://www.ncbi.nlm.nih.gov/pubmed/31798693
http://dx.doi.org/10.1177/1758835919887044
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author Miller, Emily M.
Schwartzberg, Lee S.
author_facet Miller, Emily M.
Schwartzberg, Lee S.
author_sort Miller, Emily M.
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description The utilization of trastuzumab biosimilar medications is of particular interest in HER2-positive breast cancer as these drugs have the potential for cost savings and increased utilization/access to HER2 targeted therapy in both early stage and metastatic HER2-positive breast cancers. Five trastuzumab biosimilars: MYL-1401O (Ogivri), CT-P6 (Herzuma), SB3 (Ontruzant), PF-05280014 (Trazimera), and ABP980 (Kanjinti), have now been approved by the US Food and Drug Administration (FDA) for use in HER2-positive breast cancers. This review provides an overview of these agents with special consideration of the development and approval process, including available clinical data results for these trastuzumab biosimilars. Adoption in the clinic will depend on the degree of comfort with the overall evidence.
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spelling pubmed-68596782019-12-03 Biosimilars for breast cancer: a review of HER2-targeted antibodies in the United States Miller, Emily M. Schwartzberg, Lee S. Ther Adv Med Oncol Review The utilization of trastuzumab biosimilar medications is of particular interest in HER2-positive breast cancer as these drugs have the potential for cost savings and increased utilization/access to HER2 targeted therapy in both early stage and metastatic HER2-positive breast cancers. Five trastuzumab biosimilars: MYL-1401O (Ogivri), CT-P6 (Herzuma), SB3 (Ontruzant), PF-05280014 (Trazimera), and ABP980 (Kanjinti), have now been approved by the US Food and Drug Administration (FDA) for use in HER2-positive breast cancers. This review provides an overview of these agents with special consideration of the development and approval process, including available clinical data results for these trastuzumab biosimilars. Adoption in the clinic will depend on the degree of comfort with the overall evidence. SAGE Publications 2019-11-14 /pmc/articles/PMC6859678/ /pubmed/31798693 http://dx.doi.org/10.1177/1758835919887044 Text en © The Author(s), 2019 http://www.creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (http://www.creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Review
Miller, Emily M.
Schwartzberg, Lee S.
Biosimilars for breast cancer: a review of HER2-targeted antibodies in the United States
title Biosimilars for breast cancer: a review of HER2-targeted antibodies in the United States
title_full Biosimilars for breast cancer: a review of HER2-targeted antibodies in the United States
title_fullStr Biosimilars for breast cancer: a review of HER2-targeted antibodies in the United States
title_full_unstemmed Biosimilars for breast cancer: a review of HER2-targeted antibodies in the United States
title_short Biosimilars for breast cancer: a review of HER2-targeted antibodies in the United States
title_sort biosimilars for breast cancer: a review of her2-targeted antibodies in the united states
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6859678/
https://www.ncbi.nlm.nih.gov/pubmed/31798693
http://dx.doi.org/10.1177/1758835919887044
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