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Volume 45, Issue 17, Pages 2940-2946 (November 2009)


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Activity of ixabepilone in oestrogen receptor-negative and oestrogen receptor-progesterone receptor-human epidermal growth factor receptor 2-negative metastatic breast cancer

Xavier B. PivotaCorresponding Author Informationemail address, Rubi K. Lib, Eva S. Thomasc, Hyun-Cheol Chungd, Luis E. Feine, Valorie F. Chanf, Jacek Jassemg, Fernando Hurtado de Mendozah, Pralay Mukhopadyayi, Henri H. Rochéj

Received 14 April 2009; received in revised form 18 June 2009; accepted 22 July 2009. published online 17 August 2009.

Abstract 

Oestrogen receptor (ER)-negative breast cancer, including oestrogen receptor-, progesterone receptor- and human epidermal growth factor receptor 2-negative (ER/PR/HER2-negative) breast cancer, is more aggressive than ER-positive disease. A major limitation in the treatment of ER-negative disease subtypes is the inherent insensitivity to hormonal agents (tamoxifen, aromatase inhibitors) that are widely used in the treatment of breast cancer. Thus, therapeutic options for poor prognosis patients with ER-negative breast cancer are limited to a handful of chemotherapeutic agents, and new agents are needed to improve the treatment of this disease.

Ixabepilone, a novel epothilone B analogue with low susceptibility to cellular mechanisms that confer resistance to taxanes and other chemotherapeutic agents, has demonstrated potent preclinical antitumour activity in multiple models, including those with primary or acquired drug resistance. This review summarises the results of a prospective subset analysis from a phase III clinical trial evaluating ixabepilone for the treatment of metastatic breast cancer (MBC), in which efficacy and safety were evaluated in patients with ER-negative and ER/PR/HER2-negative disease.

a Medical Oncology University Hospital, Service Oncologie, Boulevard Fleming, Besançon, Inserm U645, France

b St. Luke’s Medical Center, Quezon City, The Philippines

c Kaiser Permanente, Oakland, CA, USA

d Yonsei Cancer Center, Seoul, Republic of Korea

e Centro de Oncologia Rosario, Sante Fe, Argentina

f Veterans Memorial Medical Center, Quezon City, The Philippines

g Medical University of Gdansk, Gdansk, Poland

h Hospital Nacional Edgardo Rebagliati Martins, Lima, Peru

i Bristol-Myers Squibb, Wallingford, CT, USA

j Institut Claudius Regaud, Toulouse, France

Corresponding Author InformationCorresponding author: Tel.: +33 3 81669386; fax: +33 4 92031096.

PII: S0959-8049(09)00581-4

doi:10.1016/j.ejca.2009.07.015


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