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Durable Response to PD1 Inhibitor Pembrolizumab in a Metastatic, Metaplastic Breast Cancer
Metaplastic breast cancer (MBC) is a rare and aggressive subtype of breast cancer. Tumor characteristics typically feature estrogen receptor, progesterone receptor, and HER2-negative, triple-negative breast cancer (TNBC), with a poorer prognosis relative to pure invasive ductal or lobular disease. R...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
S. Karger AG
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8255711/ https://www.ncbi.nlm.nih.gov/pubmed/34248561 http://dx.doi.org/10.1159/000515510 |
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author | Gorshein, Elan Matsuda, Kant Riedlinger, Gregory Sokol, Levi Rodriguez-Rodriguez, Lorna Eladoumikdachi, Firas Grandhi, Miral Ganesan, Shridar Toppmeyer, Deborah L. Potdevin, Lindsay Toomey, Kathleen Hirshfield, Kim M. Chan, Nancy |
author_facet | Gorshein, Elan Matsuda, Kant Riedlinger, Gregory Sokol, Levi Rodriguez-Rodriguez, Lorna Eladoumikdachi, Firas Grandhi, Miral Ganesan, Shridar Toppmeyer, Deborah L. Potdevin, Lindsay Toomey, Kathleen Hirshfield, Kim M. Chan, Nancy |
author_sort | Gorshein, Elan |
collection | PubMed |
description | Metaplastic breast cancer (MBC) is a rare and aggressive subtype of breast cancer. Tumor characteristics typically feature estrogen receptor, progesterone receptor, and HER2-negative, triple-negative breast cancer (TNBC), with a poorer prognosis relative to pure invasive ductal or lobular disease. Resistance to chemotherapy often leads to local recurrence and distant metastasis. Genomic profiling has identified multiple molecular abnormalities that may translate to targetable therapies in MBC. These tumors are known to display higher PD-L1 expressivity than other subtypes of breast cancer, and disease control with pembrolizumab and chemotherapy has been documented. We identify a patient with metastatic, metaplastic TNBC, with mesenchymal components and osseous differentiation, who completed 2 years of pembrolizumab treatment and has remained without evidence of disease after 32 months of observation, while maintaining good quality of life. Future efforts should focus on immunotherapy response with respect to the various subtypes of MBC, and treatment should continue to be incorporated in clinical trials to maximize disease response. |
format | Online Article Text |
id | pubmed-8255711 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | S. Karger AG |
record_format | MEDLINE/PubMed |
spelling | pubmed-82557112021-07-09 Durable Response to PD1 Inhibitor Pembrolizumab in a Metastatic, Metaplastic Breast Cancer Gorshein, Elan Matsuda, Kant Riedlinger, Gregory Sokol, Levi Rodriguez-Rodriguez, Lorna Eladoumikdachi, Firas Grandhi, Miral Ganesan, Shridar Toppmeyer, Deborah L. Potdevin, Lindsay Toomey, Kathleen Hirshfield, Kim M. Chan, Nancy Case Rep Oncol Case Report Metaplastic breast cancer (MBC) is a rare and aggressive subtype of breast cancer. Tumor characteristics typically feature estrogen receptor, progesterone receptor, and HER2-negative, triple-negative breast cancer (TNBC), with a poorer prognosis relative to pure invasive ductal or lobular disease. Resistance to chemotherapy often leads to local recurrence and distant metastasis. Genomic profiling has identified multiple molecular abnormalities that may translate to targetable therapies in MBC. These tumors are known to display higher PD-L1 expressivity than other subtypes of breast cancer, and disease control with pembrolizumab and chemotherapy has been documented. We identify a patient with metastatic, metaplastic TNBC, with mesenchymal components and osseous differentiation, who completed 2 years of pembrolizumab treatment and has remained without evidence of disease after 32 months of observation, while maintaining good quality of life. Future efforts should focus on immunotherapy response with respect to the various subtypes of MBC, and treatment should continue to be incorporated in clinical trials to maximize disease response. S. Karger AG 2021-06-18 /pmc/articles/PMC8255711/ /pubmed/34248561 http://dx.doi.org/10.1159/000515510 Text en Copyright © 2021 by S. Karger AG, Basel https://creativecommons.org/licenses/by-nc/4.0/This article is licensed under the Creative Commons Attribution-NonCommercial-4.0 International License (CC BY-NC) (http://www.karger.com/Services/OpenAccessLicense). Usage and distribution for commercial purposes requires written permission. |
spellingShingle | Case Report Gorshein, Elan Matsuda, Kant Riedlinger, Gregory Sokol, Levi Rodriguez-Rodriguez, Lorna Eladoumikdachi, Firas Grandhi, Miral Ganesan, Shridar Toppmeyer, Deborah L. Potdevin, Lindsay Toomey, Kathleen Hirshfield, Kim M. Chan, Nancy Durable Response to PD1 Inhibitor Pembrolizumab in a Metastatic, Metaplastic Breast Cancer |
title | Durable Response to PD1 Inhibitor Pembrolizumab in a Metastatic, Metaplastic Breast Cancer |
title_full | Durable Response to PD1 Inhibitor Pembrolizumab in a Metastatic, Metaplastic Breast Cancer |
title_fullStr | Durable Response to PD1 Inhibitor Pembrolizumab in a Metastatic, Metaplastic Breast Cancer |
title_full_unstemmed | Durable Response to PD1 Inhibitor Pembrolizumab in a Metastatic, Metaplastic Breast Cancer |
title_short | Durable Response to PD1 Inhibitor Pembrolizumab in a Metastatic, Metaplastic Breast Cancer |
title_sort | durable response to pd1 inhibitor pembrolizumab in a metastatic, metaplastic breast cancer |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8255711/ https://www.ncbi.nlm.nih.gov/pubmed/34248561 http://dx.doi.org/10.1159/000515510 |
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