Literature DB >> 21121833

Adjuvant docetaxel for high-risk, node-negative breast cancer.

Miguel Martín1, Miguel A Seguí, Antonio Antón, Amparo Ruiz, Manuel Ramos, Encarna Adrover, Ignacio Aranda, Alvaro Rodríguez-Lescure, Regina Grosse, Lourdes Calvo, Agustí Barnadas, Dolores Isla, Purificación Martinez del Prado, Manuel Ruiz Borrego, Jerzy Zaluski, Angels Arcusa, Montserrat Muñoz, José M López Vega, José R Mel, Blanca Munarriz, Cristina Llorca, Carlos Jara, Emilio Alba, Jesús Florián, Junfang Li, José A López García-Asenjo, Amparo Sáez, María José Rios, Sergio Almenar, Gloria Peiró, Ana Lluch.   

Abstract

BACKGROUND: A regimen of docetaxel, doxorubicin, and cyclophosphamide (TAC) is superior to a regimen of fluorouracil, doxorubicin, and cyclophosphamide (FAC) when used as adjuvant therapy in women with node-positive breast cancer. The value of taxanes in the treatment of node-negative disease has not been determined.
METHODS: We randomly assigned 1060 women with axillary-node-negative breast cancer and at least one high-risk factor for recurrence (according to the 1998 St. Gallen criteria) to treatment with TAC or FAC every 3 weeks for six cycles after surgery. The primary end point was disease-free survival after at least 5 years of follow-up. Secondary end points included overall survival and toxicity.
RESULTS: At a median follow-up of 77 months, the proportion of patients alive and disease-free was higher among the 539 women in the TAC group (87.8%) than among the 521 women in the FAC group (81.8%), representing a 32% reduction in the risk of recurrence with TAC (hazard ratio, 0.68; 95% confidence interval [CI], 0.49 to 0.93; P=0.01 by the log-rank test). This benefit was consistent, regardless of hormone-receptor status, menopausal status, or number of high-risk factors. The difference in survival rates (TAC, 95.2%; FAC, 93.5%) was not significant (hazard ratio, 0.76; 95% CI, 0.45 to 1.26); however, the number of events was small (TAC, 26; FAC, 34). Rates of grade 3 or 4 adverse events were 28.2% with TAC and 17.0% with FAC (P<0.001). Toxicity associated with TAC was diminished when primary prophylaxis with granulocyte colony-stimulating factor was provided.
CONCLUSIONS: As compared with adjuvant FAC, adjuvant TAC improved the rate of disease-free survival among women with high-risk, node-negative breast cancer. (Funded by GEICAM and Sanofi-Aventis; ClinicalTrials.gov number, NCT00121992.).

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Year:  2010        PMID: 21121833     DOI: 10.1056/NEJMoa0910320

Source DB:  PubMed          Journal:  N Engl J Med        ISSN: 0028-4793            Impact factor:   91.245


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