Literature DB >> 26118876

[Advanced luminal breast cancer (hormone receptor-positive, HER2 negative): New therapeutic options in 2015].

Hélène Vanacker1, Olivia Bally1, Loay Kassem2, Olivier Tredan1, Pierre Heudel1, Thomas Bachelot3.   

Abstract

Despite improvements in early detection, surgery and systemic therapy, metastatic breast cancer remains a major cause of death. Luminal type breast cancers expressing hormone estrogen receptor (ER) or progesterone (PR) and without HER2 overexpression are generally sensitive to endocrine therapy, but raise the issue of the occurrence of resistance to treatment, particularly at metastatic stage. A better understanding of hormone resistance may guide the development of new therapeutics. New strategies aim at enhancing and prolonging of endocrine sensitivity, by optimizing existing schemes, or by combining an endocrine therapy with a targeted therapies specific to hormone resistance pathways: ER signaling, PI3K/AKT/mTOR and Cyclin Dependent Kinase (CDK). Key corners of 2014 include confirmation of benefit of high dose fulvestrant, and commercialization of everolimus as the first mTOR inhibitor in this indication. Other strategies are being tested dealing with new endocrine therapies or new molecular targets such as PI3K inhibitors, insulin-like growth factor receptor (IGF-R) and histone deacetylase (HDAC) inhibitors. Coming years may be fruitful and might radically change our way to treat these patients.
Copyright © 2015 Société Françise du Cancer. Publié par Elsevier Masson SAS. Tous droits réservés. Published by Elsevier Masson SAS. All rights reserved.

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Keywords:  Cancer du sein; Hormone; Hormone therapy; Hormonothérapie; Targeted therapy; Thérapies moléculaires; advanced breast cancer; ciblées; hormonosensible; receptor-positive

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Year:  2015        PMID: 26118876     DOI: 10.1016/S0007-4551(15)31217-0

Source DB:  PubMed          Journal:  Bull Cancer        ISSN: 0007-4551            Impact factor:   1.276


  1 in total

1.  A Flavone Constituent from Myoporum bontioides Induces M-Phase Cell Cycle Arrest of MCF-7 Breast Cancer Cells.

Authors:  Jing-Ru Weng; Li-Yuan Bai; Wei-Yu Lin; Chang-Fang Chiu; Yu-Chang Chen; Shi-Wei Chao; Chia-Hsien Feng
Journal:  Molecules       Date:  2017-03-15       Impact factor: 4.411

  1 in total

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