Cargando…

Checkpoint inhibitor therapy for metastatic triple-negative breast cancer

Immunotherapy has become a mainstay of cancer treatment in many malignancies, though its application in breast cancer remains limited. Of the breast cancer subtypes, triple-negative breast cancers (TNBCs) are characterized by immune activation and infiltration and more commonly express biomarkers as...

Descripción completa

Detalles Bibliográficos
Autores principales: Heeke, Arielle L., Tan, Antoinette R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8184866/
https://www.ncbi.nlm.nih.gov/pubmed/34101053
http://dx.doi.org/10.1007/s10555-021-09972-4
_version_ 1783704666289209344
author Heeke, Arielle L.
Tan, Antoinette R.
author_facet Heeke, Arielle L.
Tan, Antoinette R.
author_sort Heeke, Arielle L.
collection PubMed
description Immunotherapy has become a mainstay of cancer treatment in many malignancies, though its application in breast cancer remains limited. Of the breast cancer subtypes, triple-negative breast cancers (TNBCs) are characterized by immune activation and infiltration and more commonly express biomarkers associated with response to immunotherapy. Checkpoint inhibitor therapy has shown promising activity in metastatic TNBC. In 2019, the US FDA granted accelerated approval of atezolizumab, a programmed death-ligand 1 (PD-L1) inhibitor, in combination with nab-paclitaxel for unresectable locally advanced or metastatic PD-L1-positive TNBC, based on the results of the phase III IMpassion130 trial. In 2020, the FDA also granted accelerated approval of pembrolizumab, a PD-1 inhibitor, in combination with chemotherapy for locally recurrent unresectable and metastatic PD-L1-positive TNBC, based on results of the phase III KEYNOTE-355 trial. Additional combination strategies are being explored in the treatment of metastatic TNBC, with the goal of augmenting antitumor activity. In this review, the clinical development of checkpoint inhibitors in the treatment of metastatic TNBC will be discussed, including clinical outcomes with monotherapy and combination therapy regimens, biomarkers that may predict for benefit, and future directions in the field.
format Online
Article
Text
id pubmed-8184866
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher Springer US
record_format MEDLINE/PubMed
spelling pubmed-81848662021-06-08 Checkpoint inhibitor therapy for metastatic triple-negative breast cancer Heeke, Arielle L. Tan, Antoinette R. Cancer Metastasis Rev Article Immunotherapy has become a mainstay of cancer treatment in many malignancies, though its application in breast cancer remains limited. Of the breast cancer subtypes, triple-negative breast cancers (TNBCs) are characterized by immune activation and infiltration and more commonly express biomarkers associated with response to immunotherapy. Checkpoint inhibitor therapy has shown promising activity in metastatic TNBC. In 2019, the US FDA granted accelerated approval of atezolizumab, a programmed death-ligand 1 (PD-L1) inhibitor, in combination with nab-paclitaxel for unresectable locally advanced or metastatic PD-L1-positive TNBC, based on the results of the phase III IMpassion130 trial. In 2020, the FDA also granted accelerated approval of pembrolizumab, a PD-1 inhibitor, in combination with chemotherapy for locally recurrent unresectable and metastatic PD-L1-positive TNBC, based on results of the phase III KEYNOTE-355 trial. Additional combination strategies are being explored in the treatment of metastatic TNBC, with the goal of augmenting antitumor activity. In this review, the clinical development of checkpoint inhibitors in the treatment of metastatic TNBC will be discussed, including clinical outcomes with monotherapy and combination therapy regimens, biomarkers that may predict for benefit, and future directions in the field. Springer US 2021-06-08 2021 /pmc/articles/PMC8184866/ /pubmed/34101053 http://dx.doi.org/10.1007/s10555-021-09972-4 Text en © The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature 2021 This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic.
spellingShingle Article
Heeke, Arielle L.
Tan, Antoinette R.
Checkpoint inhibitor therapy for metastatic triple-negative breast cancer
title Checkpoint inhibitor therapy for metastatic triple-negative breast cancer
title_full Checkpoint inhibitor therapy for metastatic triple-negative breast cancer
title_fullStr Checkpoint inhibitor therapy for metastatic triple-negative breast cancer
title_full_unstemmed Checkpoint inhibitor therapy for metastatic triple-negative breast cancer
title_short Checkpoint inhibitor therapy for metastatic triple-negative breast cancer
title_sort checkpoint inhibitor therapy for metastatic triple-negative breast cancer
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8184866/
https://www.ncbi.nlm.nih.gov/pubmed/34101053
http://dx.doi.org/10.1007/s10555-021-09972-4
work_keys_str_mv AT heekeariellel checkpointinhibitortherapyformetastatictriplenegativebreastcancer
AT tanantoinetter checkpointinhibitortherapyformetastatictriplenegativebreastcancer