Abstract
Triple negative breast cancer (TNBC), an aggressive breast cancer subtype lacking estrogen receptor (ER), progesterone receptor, and human epidermal growth factor receptor 2 (HER2) expression, is associated with heightened metastatic potential and poor prognosis. While systemic chemotherapy, radiation, and surgical excision remain the current treatment modalities for patients with TNBC, the immunogenic nature of this aggressive disease has presented opportunity for the development of TNBC-targeting immunotherapies. Bispecific antibody-based therapeutics for the treatment of TNBC have gained recent attention in the scientific community. Clinical precedent has been previously established for the FDA-approved bispecific T cell engager, blinatumomab, for acute lymphoblastic leukemia. The present review discusses novel bispecific antibodies for TNBC and emerging TNBC targets for future bispecific antibody development.
Keywords:
T cell redirection; bispecific antibodies; breast cancer; immunotherapy; triple negative breast cancer.
Copyright © 2020 Elsevier Inc. All rights reserved.
MeSH terms
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Antibodies, Bispecific / pharmacology
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Antibodies, Bispecific / therapeutic use*
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Antibodies, Monoclonal, Humanized / pharmacology
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Antibodies, Monoclonal, Humanized / therapeutic use
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Antineoplastic Agents, Immunological / pharmacology
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Antineoplastic Agents, Immunological / therapeutic use*
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Camptothecin / analogs & derivatives
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Camptothecin / pharmacology
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Camptothecin / therapeutic use
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Clinical Trials as Topic
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Female
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Humans
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Immune Checkpoint Inhibitors / pharmacology
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Immune Checkpoint Inhibitors / therapeutic use*
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Immunoconjugates / pharmacology
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Immunoconjugates / therapeutic use
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Medical Oncology / methods
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Medical Oncology / trends
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Molecular Targeted Therapy / methods
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Survival Rate
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T-Lymphocytes, Cytotoxic / drug effects
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T-Lymphocytes, Cytotoxic / immunology
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Treatment Outcome
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Triple Negative Breast Neoplasms / drug therapy*
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Triple Negative Breast Neoplasms / immunology
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Triple Negative Breast Neoplasms / mortality
Substances
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Antibodies, Bispecific
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Antibodies, Monoclonal, Humanized
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Antineoplastic Agents, Immunological
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Immune Checkpoint Inhibitors
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Immunoconjugates
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atezolizumab
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sacituzumab govitecan
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Camptothecin