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Extended Benefit from Sequential Administration of Docetaxel after Standard Fluorouracil, Epirubicin, and Cyclophosphamide Regimen for Node-Positive Breast Cancer: The 8-Year Follow-Up Results of the UNICANCER-PACS01 Trial.

Authors :
COUDERT, BRUNO
ASSELAIN, BERNARD
CAMPONE, MARIO
SPIELMANN, MARC
MACHIELS, JEAN-PASCAL
PÉNAULT-LLORCA, FRÉDÉRIQUE
SERIN, DANIEL
LÉVY, CHRISTELLE
ROMIEU, GILLES
CANON, JEAN-LUC
ORFEUVRE, HUBERT
PIOT, GILLES
PETIT, THIERRY
JERUSALEM, GUY
AUDHUY, BRUNO
VEYRET, CORINNE
BEAUDUIN, MARC
EYMARD, JEAN-CHRISTOPHE
MARTIN, ANNE-LAURE
ROCHÉ, HENRI
Source :
Oncologist; Jul2012, Vol. 17 Issue 7, p900-909, 10p, 4 Charts, 2 Graphs
Publication Year :
2012

Abstract

Patients and Methods. Between June 1997 and March 2000, a total of 1,999 patients (age <65) with localized, resectable, non-pretreated, unilateral breast cancer were randomly assigned to receive either standard FEC100 for 6 cycles or 3 cycles of FEC100 followed by 3 cycles of 100 mg/m<superscript>2</superscript> docetaxel (FEC-D), both given every 21 days. Radiotherapy was mandatory after conservative surgery and tamoxifen was given for 5 years to hormone receptor (HR)- positive patients. Five-year DFS was the trial's main endpoint. Updated 8-year survival data are presented. Results. With a median follow-up of 92.8 months, 639 patients experienced at least one event. A total number of 383 deaths were registered. Eight-year DFS rates were 65.8% with FEC alone and 70.2% with FEC-D. OS rates at 8 years were 78% with FEC alone and 83.2% with FEC-D. Cox regression analysis adjusted for age and number of positive nodes showed a 15% reduction in the relative risk of relapse and a 25% reduction in the relative risk of death in favor of FEC-D. Significant relative risk reductions were observed in the HR-positive, HER2-positive, and Ki67≥20% subpopulations. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
10837159
Volume :
17
Issue :
7
Database :
Complementary Index
Journal :
Oncologist
Publication Type :
Academic Journal
Accession number :
78317115
Full Text :
https://doi.org/10.1634/theoncologist.2011-0442