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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: S. Karger AG 2021
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.
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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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