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Epirubicin and cyclophosphamide, methotrexate, and fluorouracil as adjuvant therapy for early breast cancer

By Christopher J. Poole, Helena M. Earl, Louise Hiller, Janet A. Dunn, Sarah Bathers, Robert J. Grieve, David A. Spooner, Rajiv K. Agrawal, Indrajit N. Fernando, A. Murray Brunt, Susan M. O'Reilly, S. Michael Crawford, Daniel W. Rea, Peter Simmonds, Janine L. Mansi, Andrew Stanley, Peter Harvey, Karen McAdam, Liz Foster, Robert C.F. Leonard and for the NEAT Investigators and the SCTBG Christopher J. Twelves

Abstract

Background The National Epirubicin Adjuvant Trial (NEAT) and the BR9601 trial examined the efficacy of anthracyclines in the adjuvant treatment of early breast cancer. <br/>Methods In NEAT, we compared four cycles of epirubicin followed by four cycles of cyclophosphamide, methotrexate, and fluorouracil (CMF) with six cycles of CMF alone. In the BR9601 trial, we compared four cycles of epirubicin followed by four cycles of CMF, with eight cycles of CMF alone every 3 weeks. The primary end points were relapse-free and overall survival. The secondary end points were adverse effects, dose intensity, and quality of life. <br/>Results The two trials included 2391 women with early breast cancer; the median follow-up was 48 months. Relapse-free and overall survival rates were significantly higher in the epirubicin–CMF groups than in the CMF-alone groups (2-year relapse-free survival, 91% vs. 85%; 5-year relapse-free survival, 76% vs. 69%; 2-year overall survival, 95% vs. 92%; 5-year overall survival, 82% vs. 75%; P&lt;0.001 by the log-rank test for all comparisons). Hazard ratios for relapse (or death without relapse) (0.69; 95% confidence interval [CI], 0.58 to 0.82; P&lt;0.001) and death from any cause (0.67; 95% CI, 0.55 to 0.82; P&lt;0.001) favored epirubicin plus CMF over CMF alone. Independent prognostic factors were nodal status, tumor grade, tumor size, and estrogen-receptor status (P&lt;0.001 for all four factors) and the presence or absence of vascular or lymphatic invasion (P=0.01). These factors did not significantly interact with the effect of epirubicin plus CMF. The overall incidence of adverse effects was significantly higher with epirubicin plus CMF than with CMF alone but did not significantly affect the delivered-dose intensity or the quality of life. <br/>Conclusions Epirubicin plus CMF is superior to CMF alone as adjuvant treatment for early breast cancer

Topics: RM, RC0254
Year: 2006
OAI identifier: oai:eprints.soton.ac.uk:44624
Provided by: e-Prints Soton
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