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Summary
June 2005, Vol. 6, No. 7, Pages 1073-1094
, DOI 10.1517/14656566.6.7.1073
The role of taxanes in the treatment of breast cancerJean-Marc Nabholtz1La PrandieBreast Cancer Research Institute, , 24290 Valojoulx, France. jmnabholtz@hotmail.com 2CancerEst APHP Tenon, Medical Oncology Department 4, Rue de la Chine, 75970 Paris Cedex 20, France Among the novel chemotherapeutic agents introduced in the last decade, the taxanes have emerged as the most powerful group of compounds, and results available so far confirm that they will be remembered in the future as the breast cancer chemotherapy of the 1990s. Two taxanes are available (paclitaxel and docetaxel) and they share some characteristics, although they do have some significant differences both in terms of their preclinical profile and, most importantly, their clinical characteristics. There are three main clinical differences: different efficacy–toxicity ratio in relation to dose and schedule; different integrability in anthracycline- and taxane-containing regimens, secondary to differences in pharmacokinetic interactions with anthracyclines; and different level of synergism between each taxane and trastuzumab. In clinical practice, the taxanes are now standard therapy in metastatic breast cancer. Their role as monochemotherapy or in combination with anthracyclines in advanced breast cancer has suggested their potential therapeutic impact in the treatment of patients with early breast cancer. Recent results in the adjuvant setting show that taxanes, used either in combination or in sequential therapy, possess the capability to induce significant improvements, in particular in terms of survival; thus confirming the positive impact of taxanes on the natural history of breast cancer. However, further results of all completed or ongoing Phase III trials in the early setting will help define the optimal use of taxanes and maximise the induced benefits for breast cancer patients. Forward Links to Citing ArticlesPaul A. Foster, Yaik T. Ho, Simon P. Newman, Philip G. Kasprzyk, Mathew P. Leese, Barry V. L. Potter, Michael J. Reed, Atul Purohit. (2008) 2-MeOE2bisMATE and 2-EtE2bisMATE induce cell cycle arrest and apoptosis in breast cancer xenografts as shown by a novel ex vivo technique. Breast Cancer Research and Treatment 111:2, 251-260 Online publication date: 1-Oct-2008. CrossRef Rajeshwar P. Verma, Corwin Hansch. (2008) Taxane Analogues against Breast Cancer: A Quantitative Structure–Activity Relationship Study. ChemMedChem 3:4, 642-652Online publication date: 14-May-2008. CrossRef Neelima Denduluri, Sandra M Swain. (2008) Ixabepilone for the treatment of solid tumors: a review of clinical data. Expert Opinion on Investigational Drugs 17:3, 423-435 Online publication date: 1-Mar-2008. Summary | Full Text | PDF (146 KB) | PDF Plus (231 KB) Sharon Marsh, Howard L McLeod. (2007) Pharmacogenetics and oncology treatment for breast cancer. Expert Opinion on Pharmacotherapy 8:2, 119-127 Online publication date: 1-Feb-2007. Summary | Full Text | PDF (173 KB) | PDF Plus (328 KB) Michael C Cox, Tu D Dan, Sandra M Swain. (2006) Emerging drugs to replace current leaders in first-line therapy for breast cancer. Expert Opinion on Emerging Drugs 11:3, 489-501 Online publication date: 1-Sep-2006. Summary | Full Text | PDF (144 KB) | PDF Plus (290 KB) Debra Patt, Michelle Gauthier, Sharon Giordano. (2006) Paclitaxel in breast cancer. Women s Health 2:1, 11 CrossRef |
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Author for correspondence
P. Verma
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