Literature DB >> 17485906

Recent perspectives of endocrine therapy for breast cancer.

Toshiaki Utsumi1, Naomi Kobayashi, Hidetaka Hanada.   

Abstract

The choice of endocrine therapy for breast cancer depends on the menopausal status and stage of disease. Endocrine therapy remains the first choice and most important component in the treatment of hormone sensitive non-life threatening advanced breast cancer. In premenopausal women with metastatic disease, the combination of a luteinizing hormone-releasing hormone (LH-RH) agonist plus tamoxifen is reasonable as first-line endocrine therapy. In postmenopausal patients with recurrent disease progressing after or during adjuvant tamoxifen, third-generation aromatase inhibitors (AIs) are the preferred first-line endocrine treatment. Many premenopausal and postmenopausal women with hormone responsive breast cancer benefit from sequential use of endocrine therapies at the time of disease progression. Recent clinical trials designs have been implemented, employing AIs as monotherapy in postmenopausal breast cancer patients, as first-line adjuvant therapy, and in sequence either 2-3 or 5 years, with initial tamoxifen. Emerging results from these trials indicate an advantage to patients for any of these strategies, and most international guidelines now suggest the use of an AI in the adjuvant setting in postmenopausal women. The use of endocrine treatment for metastatic and early breast cancer will be reviewed here.

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Year:  2007        PMID: 17485906     DOI: 10.2325/jbcs.959

Source DB:  PubMed          Journal:  Breast Cancer        ISSN: 1340-6868            Impact factor:   4.239


  13 in total

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Authors:  V Cortez; M Mann; D W Brann; R K Vadlamudi
Journal:  Minerva Ginecol       Date:  2010-12

Review 2.  Intrinsic cancer subtypes--next steps into personalized medicine.

Authors:  Cristina Santos; Rebeca Sanz-Pamplona; Ernest Nadal; Julieta Grasselli; Sonia Pernas; Rodrigo Dienstmann; Victor Moreno; Josep Tabernero; Ramon Salazar
Journal:  Cell Oncol (Dordr)       Date:  2015-01-14       Impact factor: 6.730

3.  TCR-dependent transformation of mature memory phenotype T cells in mice.

Authors:  Xi Wang; Miriam B F Werneck; Boris G Wilson; Hye-Jung Kim; Michael J Kluk; Christopher S Thom; Jonathan W Wischhusen; Julia A Evans; Jonathan L Jesneck; Phuong Nguyen; Courtney G Sansam; Harvey Cantor; Charles W M Roberts
Journal:  J Clin Invest       Date:  2011-09-19       Impact factor: 14.808

4.  Significance of PELP1 in ER-negative breast cancer metastasis.

Authors:  Sudipa Roy; Dimple Chakravarty; Valerie Cortez; Keya De Mukhopadhyay; Abhik Bandyopadhyay; Jung-Mo Ahn; Ganesh V Raj; Rajeshwar R Tekmal; LuZhe Sun; Ratna K Vadlamudi
Journal:  Mol Cancer Res       Date:  2011-11-15       Impact factor: 5.852

5.  Extranuclear functions of ER impact invasive migration and metastasis by breast cancer cells.

Authors:  Dimple Chakravarty; Sujit S Nair; Bindu Santhamma; Binoj C Nair; Long Wang; Abhik Bandyopadhyay; Joseph K Agyin; Darrell Brann; Lu-Zhe Sun; I-Tien Yeh; Francis Y Lee; Rajeshwar Rao Tekmal; Rakesh Kumar; Ratna K Vadlamudi
Journal:  Cancer Res       Date:  2010-05-11       Impact factor: 12.701

6.  Uterine changes during tamoxifen, toremifene, and other therapy for breast cancer: evaluation with magnetic resonance imaging.

Authors:  Junko Ochi; Katsumi Hayakawa; Yoshio Moriguchi; Yoji Urata; Akira Yamamoto; Kanae Kawai
Journal:  Jpn J Radiol       Date:  2010-07-27       Impact factor: 2.374

7.  c-MYC-regulated miR-23a/24-2/27a cluster promotes mammary carcinoma cell invasion and hepatic metastasis by targeting Sprouty2.

Authors:  Xiaoni Li; Xin Liu; Weiyi Xu; Peng Zhou; Ping Gao; Songshan Jiang; Peter E Lobie; Tao Zhu
Journal:  J Biol Chem       Date:  2013-05-06       Impact factor: 5.157

8.  Targeting the PELP1-KDM1 axis as a potential therapeutic strategy for breast cancer.

Authors:  Valerie Cortez; Monica Mann; Seshidhar Tekmal; Takayoshi Suzuki; Naoki Miyata; Cristian Rodriguez-Aguayo; Gabriel Lopez-Berestein; Anil K Sood; Ratna K Vadlamudi
Journal:  Breast Cancer Res       Date:  2012-07-19       Impact factor: 6.466

9.  Glibenclamide inhibits cell growth by inducing G0/G1 arrest in the human breast cancer cell line MDA-MB-231.

Authors:  Mariel Núñez; Vanina Medina; Graciela Cricco; Máximo Croci; Claudia Cocca; Elena Rivera; Rosa Bergoc; Gabriela Martín
Journal:  BMC Pharmacol Toxicol       Date:  2013-01-11       Impact factor: 2.483

10.  Fulvestrant-induced cell death and proteasomal degradation of estrogen receptor α protein in MCF-7 cells require the CSK c-Src tyrosine kinase.

Authors:  Wei-Lan Yeh; Keiko Shioda; Kathryn R Coser; Danielle Rivizzigno; Kristen R McSweeney; Toshi Shioda
Journal:  PLoS One       Date:  2013-04-04       Impact factor: 3.240

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