Literature DB >> 21778572

Current treatment options in triple negative breast cancer.

Eve Rodler1, Larissa Korde, Julie Gralow.   

Abstract

Triple negative breast cancer (TNBC) refers to a subgroup of breast carcinomas that do not express the estrogen receptor, progesterone receptor, or human epidermal growth factor receptor type 2. This heterogeneous group of tumors has significant overlap with both basal-like tumors (defined through gene expression array) and BRCA1 mutation-associated tumors. Due to a lack of well defined clinical targets, chemotherapy is the standard of care treatment for TNBC. When compared with other breast cancer subtypes, TNBC exhibits at least equivalent, or often superior sensitivity to chemotherapy. However, despite this increased chemosensitivity, TNBC has a worse clinical outcome than other breast cancer subtypes. This has led to the investigation of DNA damaging chemotherapy agents, including platinum drugs, angiogenesis inhibitors, poly(ADP-ribose) polymerase inhibitors, novel microtubule inhibitors, and other targeted therapies in an effort to improve the outcome for patients with these high-risk tumors. Treatment decisions for patients with TNBC should be based on the best currently available evidence, which consists mainly of retrospective and prospective subgroup analyses and phase II prospective data. This review summarizes data from select neoadjuvant, adjuvant, and metastatic chemotherapy clinical trials which included analyses of treatment effects and outcomes in TNBC and/or basal-like breast cancer.

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Year:  2010        PMID: 21778572     DOI: 10.3233/BD-2010-0304

Source DB:  PubMed          Journal:  Breast Dis        ISSN: 0888-6008


  21 in total

1.  Loss of monocyte chemoattractant protein-1 expression delays mammary tumorigenesis and reduces localized inflammation in the C3(1)/SV40Tag triple negative breast cancer model.

Authors:  Taryn L Cranford; Kandy T Velázquez; Reilly T Enos; Jackie E Bader; Meredith S Carson; Ioulia Chatzistamou; Mitzi Nagarkatti; E Angela Murphy
Journal:  Cancer Biol Ther       Date:  2017-01-11       Impact factor: 4.742

2.  Metabolic role of fatty acid binding protein 7 in mediating triple-negative breast cancer cell death via PPAR-α signaling.

Authors:  Soke Chee Kwong; Amira Hajirah Abd Jamil; Anthony Rhodes; Nur Aishah Taib; Ivy Chung
Journal:  J Lipid Res       Date:  2019-09-04       Impact factor: 5.922

3.  The FGF/FGFR axis as a therapeutic target in breast cancer.

Authors:  Nicholas Brady; Polly Chuntova; Lindsey K Bade; Kathryn L Schwertfeger
Journal:  Expert Rev Endocrinol Metab       Date:  2013-07

4.  Piperlongumine for Enhancing Oral Bioavailability and Cytotoxicity of Docetaxel in Triple-Negative Breast Cancer.

Authors:  Ketan Patel; Nusrat Chowdhury; Ravi Doddapaneni; Cedar H A Boakye; Chandraiah Godugu; Mandip Singh
Journal:  J Pharm Sci       Date:  2015-09-15       Impact factor: 3.534

5.  Doxorubicin-Hyaluronan Conjugated Super-Paramagnetic Iron Oxide Nanoparticles (DOX-HA-SPION) Enhanced Cytoplasmic Uptake of Doxorubicin and Modulated Apoptosis, IL-6 Release and NF-kappaB Activity in Human MDA-MB-231 Breast Cancer Cells.

Authors:  Dinesh Vyas; Nicolas Lopez-Hisijos; Sulakshana Gandhi; M El-Dakdouki; Marc D Basson; Mary F Walsh; X Huang; Arpita K Vyas; Lakshmi S Chaturvedi
Journal:  J Nanosci Nanotechnol       Date:  2015-09

6.  Platinum-based therapy for triple-negative breast cancer treatment: A meta-analysis.

Authors:  Muyou Tian; Yahua Zhong; Fuxiang Zhou; Conghua Xie; Yunfeng Zhou; Zhengkai Liao
Journal:  Mol Clin Oncol       Date:  2015-02-26

7.  Peptidomimetic Src/pretubulin inhibitor KX-01 alone and in combination with paclitaxel suppresses growth, metastasis in human ER/PR/HER2-negative tumor xenografts.

Authors:  Muralidharan Anbalagan; Alaa Ali; Ryan K Jones; Carolyn G Marsden; Mei Sheng; Latonya Carrier; Yahao Bu; David Hangauer; Brian G Rowan
Journal:  Mol Cancer Ther       Date:  2012-07-10       Impact factor: 6.261

8.  CDK4/6 inhibition antagonizes the cytotoxic response to anthracycline therapy.

Authors:  A Kathleen McClendon; Jeffry L Dean; Dayana B Rivadeneira; Justine E Yu; Christopher A Reed; Erhe Gao; John L Farber; Thomas Force; Walter J Koch; Erik S Knudsen
Journal:  Cell Cycle       Date:  2012-07-15       Impact factor: 4.534

9.  Prospective study of cyclophosphamide, thiotepa, carboplatin combined with adoptive DC-CIK followed by metronomic cyclophosphamide therapy as salvage treatment for triple negative metastatic breast cancers patients (aged <45).

Authors:  X Wang; J Ren; J Zhang; Y Yan; N Jiang; J Yu; L Di; G Song; L Che; J Jia; X Zhou; H Yang; H K Lyerly
Journal:  Clin Transl Oncol       Date:  2015-08-13       Impact factor: 3.405

10.  Expression of a novel peptide derived from PCNA damages DNA and reverses cisplatin resistance.

Authors:  Robert G Lingeman; Robert J Hickey; Linda H Malkas
Journal:  Cancer Chemother Pharmacol       Date:  2014-09-05       Impact factor: 3.333

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