Literature DB >> 16504510

Postmenopausal advanced breast cancer: options for therapy after tamoxifen and aromatase inhibitors.

D Dodwell1, A Wardley, S Johnston.   

Abstract

All patients receiving endocrine treatment for advanced breast cancer (ABC) eventually progress, resulting in a need for new therapies that lack cross-resistance with existing agents. Oestrogen receptor (ER) modulators such as toremifene and raloxifene have poor efficacy following tamoxifen failure, whereas the non-steroidal aromatase inhibitors (AIs), anastrozole and letrozole and the steroidal AI exemestane are effective. Fulvestrant is a new ER antagonist with no agonist effects that is as effective as anastrozole in treating patients who have progressed on tamoxifen. AIs are replacing tamoxifen as first-line treatments for ABC and in the adjuvant setting, necessitating a re-evaluation of optimal sequencing. Preliminary data suggest that tamoxifen, exemestane and fulvestrant have activity in patients who have progressed on non-steroidal AIs and hence could be considered for use in this setting. Due to the apparent lack of cross-resistance between non-steroidal and steroidal AIs, non-steroidal AIs could also be effective following steroidal AI failure. Clinical trials are underway to assess the most appropriate treatment sequence following non-steroidal AI failure, with comparisons of fulvestrant and exemestane of major interest.

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Year:  2006        PMID: 16504510     DOI: 10.1016/j.breast.2006.01.007

Source DB:  PubMed          Journal:  Breast        ISSN: 0960-9776            Impact factor:   4.380


  17 in total

Review 1.  The changing role of ER in endocrine resistance.

Authors:  Agostina Nardone; Carmine De Angelis; Meghana V Trivedi; C Kent Osborne; Rachel Schiff
Journal:  Breast       Date:  2015-08-10       Impact factor: 4.380

Review 2.  ESR1 mutations—a mechanism for acquired endocrine resistance in breast cancer.

Authors:  Rinath Jeselsohn; Gilles Buchwalter; Carmine De Angelis; Myles Brown; Rachel Schiff
Journal:  Nat Rev Clin Oncol       Date:  2015-06-30       Impact factor: 66.675

Review 3.  Mechanisms of endocrine resistance in breast cancer.

Authors:  C Kent Osborne; Rachel Schiff
Journal:  Annu Rev Med       Date:  2011       Impact factor: 13.739

4.  The turnover of estrogen receptor α by the selective estrogen receptor degrader (SERD) fulvestrant is a saturable process that is not required for antagonist efficacy.

Authors:  Suzanne E Wardell; Jeffrey R Marks; Donald P McDonnell
Journal:  Biochem Pharmacol       Date:  2011-04-09       Impact factor: 5.858

5.  Endocrine Therapy-related Endocrinopathies-Biology, Prevalence and Implications for the Management of Breast Cancer.

Authors:  Kristy A Brown; Eleni Andreopoulou; Panagiota Andreopoulou
Journal:  Oncol Hematol Rev       Date:  2020-02-16

6.  Bazedoxifene exhibits antiestrogenic activity in animal models of tamoxifen-resistant breast cancer: implications for treatment of advanced disease.

Authors:  Suzanne E Wardell; Erik R Nelson; Christina A Chao; Donald P McDonnell
Journal:  Clin Cancer Res       Date:  2013-03-27       Impact factor: 12.531

Review 7.  Endocrine-Resistant Breast Cancer: Mechanisms and Treatment.

Authors:  Andreas D Hartkopf; Eva-Maria Grischke; Sara Y Brucker
Journal:  Breast Care (Basel)       Date:  2020-07-29       Impact factor: 2.860

Review 8.  Management of adverse events in patients with hormone receptor-positive breast cancer treated with everolimus: observations from a phase III clinical trial.

Authors:  Mary E Peterson
Journal:  Support Care Cancer       Date:  2013-05-19       Impact factor: 3.603

9.  Everolimus plus exemestane versus bevacizumab-based chemotherapy for second-line treatment of hormone receptor-positive metastatic breast cancer in Greece: An economic evaluation study.

Authors:  Georgia Kourlaba; Vasiliki Rapti; Athanasios Alexopoulos; John Relakis; Georgios Koumakis; Magdalini Chatzikou; Nikos Maniadakis; Vassilis Georgoulias
Journal:  BMC Health Serv Res       Date:  2015-08-05       Impact factor: 2.655

10.  Aurora-A mitotic kinase induces endocrine resistance through down-regulation of ERα expression in initially ERα+ breast cancer cells.

Authors:  Mateusz Opyrchal; Jeffrey L Salisbury; Shuya Zhang; James McCubrey; John Hawse; Mattew P Goetz; Gwen A Lomberk; Tufia Haddad; Amy Degnim; Carol Lange; James N Ingle; Evanthia Galanis; Antonino B D'Assoro
Journal:  PLoS One       Date:  2014-05-09       Impact factor: 3.240

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