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Long-term follow-up of the SBG 9401 study comparing tailored FEC-based therapy versus marrow-supported high-dose therapy

Authors :
Carl Blomqvist
Henrik Lindman
N. O. Bengtsson
Gun Anker
Jonas Bergh
Per Ljungman
Johan Nilsson
Bjørn Erikstein
Harald Holte
Elisabet Lidbrink
Per-Uno Malmström
T. Wiklund
G. Söderlund
Erik Wist
P-L Kellokumpu-Lehtinen
Nils Wilking
Eeva Salminen
S. Ottosson
Source :
Annals of Oncology. 18:694-700
Publication Year :
2007
Publisher :
Elsevier BV, 2007.

Abstract

Background: The purpose was to investigate adjuvant marrow-supportive high-dose chemotherapy compared with an equitoxicity-tailored comparator arm. Patients and methods: Five hundred and twenty-five women below the age of 60 years with operated high-risk primary breast cancer were randomised to nine cycles of granulocyte colony-stimulating factor supported and individually tailored FEC (5-fluorouracil, epirubicin, cyclophosphamide), (n = 251) or standard FEC followed by marrow-supported high-dose therapy with CTCb (cyclophosphamide, thiotepa, carboplatin) therapy (n = 274), followed by locoregional radiotherapy and tamoxifen for 5 years. Results: There were 104 breast cancer relapses in the tailored FEC group versus 139 in the CTCb group (double triangular method by Whitehead, P = 0.046), with a median follow-up of all included patients of 60.8 months. The event-free survival demonstrated 121 and 150 events in the tailored FEC- and CTCb group, respectively [P = 0.074, hazard ratio (HR) 0.804, 95% confidence interval (CI) 0.633-1.022]. Ten patients in the tailored FEC regimen developed acute myeloid leukaemia (AML)/myelodysplasia (MDS). One hundred deaths occurred in the tailored FEC group and 121 in the CTCb group (P = 0.287, HR 0.866, 95% CI 0.665-1.129). Conclusion: The update of this study shows an improved outcome linked to the tailored FEC treatment in relation to breast cancer relapse, but also an increased incidence of AML/MDS. (Less)

Details

ISSN :
09237534
Volume :
18
Database :
OpenAIRE
Journal :
Annals of Oncology
Accession number :
edsair.doi.dedup.....75724032fb8c97c83a76b4549ea9da6d
Full Text :
https://doi.org/10.1093/annonc/mdl488