Literature DB >> 33781662

Advances in Therapeutic Approaches for Triple-Negative Breast Cancer.

Reshma Mahtani1, Muaiad Kittaneh2, Kevin Kalinsky3, Eleftherios Mamounas4, Sunil Badve5, Charles Vogel6, Elyse Lower7, Lee Schwartzberg8, Mark Pegram9.   

Abstract

Triple-negative breast cancer (TNBC), defined as breast cancer lacking expression of estrogen receptor, progesterone receptor, and human epidermal growth factor receptor 2 (HER2), accounts for up to 20% of all breast cancer, and it occurs at a higher frequency in younger, African American, and Hispanic women. Compared to breast cancers that are hormone receptor and/or HER2 positive, TNBC has an aggressive clinical course and worse prognosis. Because TNBC is by definition unresponsive to endocrine therapy (eg, tamoxifen, aromatase inhibitors) and HER2-directed therapies (eg, trastuzumab), chemotherapy continues to play an important role. TNBC constitutes a molecularly heterogeneous group of tumors that can vary in response to treatment, and clinical management can be challenging, particularly for the practicing community oncologist, for whom breast cancer may be only one of many tumor types encountered. In January 2020, the Breast Cancer Therapy Expert Group (BCTEG) convened a roundtable discussion on the topic of advances in the treatment of TNBC. Topics discussed included histopathologic classification/definition of TNBC, neoadjuvant strategies, adjuvant chemotherapy (with special emphasis on management of patients who do not experience a pathologic complete response), and treatment of metastatic disease. Also reviewed was the wide range of emerging pathways and therapies currently under investigation to expand TNBC treatment options, including immunotherapies and poly(ADP-ribose) polymerase (PARP) inhibitors. This article summarizes the BCTEG discussion and highlights the key opinions relating to the treatment of patients with TNBC.
Copyright © 2020. Published by Elsevier Inc.

Entities:  

Keywords:  BRCA mutation; Breast Cancer Therapy Expert Group; Immunotherapy; PARP inhibitor; Sacituzumab govitecan

Mesh:

Substances:

Year:  2020        PMID: 33781662     DOI: 10.1016/j.clbc.2020.12.011

Source DB:  PubMed          Journal:  Clin Breast Cancer        ISSN: 1526-8209            Impact factor:   3.225


  4 in total

1.  A Marine λ-Oligocarrageenan Inhibits Migratory and Invasive Ability of MDA-MB-231 Human Breast Cancer Cells through Actions on Heparanase Metabolism and MMP-14/MMP-2 Axis.

Authors:  Rémi Cousin; Hugo Groult; Chanez Manseur; Romain Ferru-Clément; Mario Gani; Rachel Havret; Claire Toucheteau; Grégoire Prunier; Béatrice Colin; Franck Morel; Jean-Marie Piot; Isabelle Lanneluc; Kévin Baranger; Thierry Maugard; Ingrid Fruitier-Arnaudin
Journal:  Mar Drugs       Date:  2021-09-28       Impact factor: 5.118

2.  Ceritinib is a novel triple negative breast cancer therapeutic agent.

Authors:  Shengli Dong; Hassan Yousefi; Isabella Van Savage; Samuel C Okpechi; Maryl K Wright; Margarite D Matossian; Bridgette M Collins-Burow; Matthew E Burow; Suresh K Alahari
Journal:  Mol Cancer       Date:  2022-06-29       Impact factor: 41.444

Review 3.  Persistent EGFR/K-RAS/SIAH pathway activation drives chemo-resistance and early tumor relapse in triple-negative breast cancer.

Authors:  Amy H Tang; Richard A Hoefer; Mary L Guye; Harry D Bear
Journal:  Cancer Drug Resist       Date:  2022-06-22

Review 4.  OB-Folds and Genome Maintenance: Targeting Protein-DNA Interactions for Cancer Therapy.

Authors:  Sui Par; Sofia Vaides; Pamela S VanderVere-Carozza; Katherine S Pawelczak; Jason Stewart; John J Turchi
Journal:  Cancers (Basel)       Date:  2021-07-03       Impact factor: 6.639

  4 in total

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