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A randomised factorial trial of sequential doxorubicin and CMF vs CMF and chemotherapy alone vs chemotherapy followed by goserelin plus tamoxifen as adjuvant treatment of node-positive breast cancer

Authors :
DE PLACIDO, SABINO
DE LAURENTIIS, MICHELINO
LAURIA, ROSSELLA
PETRELLA, GIUSEPPE
LIMITE, GENNARO
COSTANZO, RAFFAELE
DE LENA M
LORUSSO V
PARADISO A
D'APRILE M
PISTILLUCCI G
FARRIS A
SAROBBA MG
PALAZZO S
MANZIONE L
ADAMO V
PALMERI S
FERRAU F
PAGLIARULO C
BIANCO AR
GOCSI COOPERATIVE G.R.O.U.P.
DE PLACIDO, Sabino
DE LAURENTIIS, Michelino
DE LENA, M
Lorusso, V
Paradiso, A
D'Aprile, M
Pistillucci, G
Farris, A
Sarobba, Mg
Palazzo, S
Manzione, L
Adamo, V
Palmeri, S
Ferrau, F
Lauria, Rossella
Pagliarulo, C
Petrella, Giuseppe
Limite, Gennaro
Costanzo, Raffaele
Bianco, Ar
GOCSI COOPERATIVE, G. R. O. U. P.
Publication Year :
2005
Publisher :
Editore attuale:NATURE PUBLISHING GROUP, MACMILLAN BUILDING, 4 CRINAN ST, LONDON, ENGLAND, N1 9XW Harcourt Publishers Limited:Foots Cray High Street, Sidcup Kent DA14 5HP United Kingdom:011 44 20 83085700, EMAIL: journals@harcourt.com, INTERNET: http://www.harcourt-international.com, Fax: 011 44 20 83085876, 2005.

Abstract

The sequential doxorubicin --> CMF (CMF=cyclophosphamide, methotrexate, fluorouracil) regimen has never been compared to CMF in a randomised trial. The role of adding goserelin and tamoxifen after chemotherapy is unclear. In all, 466 premenopausal node-positive patients were randomised to: (a) CMF x 6 cycles (CMF); (b) doxorubicin x 4 cycles followed by CMF x 6 cycles (A --> CMF); (c) CMF x 6 cycles followed by goserelin plus tamoxifen x 2 years (CMF --> GT); and (d) doxorubicin x 4 cycles followed by CMF x 6 cycles followed by goserelin plus tamoxifen x 2 years (A --> CMF --> GT). The study used a 2 x 2 factorial experimental design to assess: (1) the effect of the chemotherapy regimens (CMF vs A --> CMF or arms a+c vs b+d) and (2) the effect of adding GT after chemotherapy (arms a+b vs c+d). At a median follow-up of 72 months, A --> CMF as compared to CMF significantly improved disease-free survival (DFS) with a multivariate hazard ratio (HR)=0.740 (95\% confidence interval (CI): 0.556-0.986; P=0.040) and produced a nonsignificant improvement of overall survival (OS) (HR=0.764; 95\% CI: 0.489-1.193). The addition of GT after chemotherapy significantly improved DFS (HR=0.74; 95\% CI: 0.555-0.987; P=0.040), with a nonsignificant improvement of OS (HR=0.84; 95\% CI: 0.54-1.32). A --> CMF is superior to CMF. Adding GT after chemotherapy is beneficial for premenopausal node-positive patients..

Details

Database :
OpenAIRE
Accession number :
edsair.od......3730..14ea7abbd07390e1b30c250579199fb7